
Overview
overview
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Joe Leigh Simpson, M.D., FACOG, FACMG, FRCOG, received his undergraduate and medical education at Duke University (M.D., 1968) and post graduate training at Cornell University Medical College (New York City). Academic positions have included: Professor at Northwestern University (1975-1986), Professor and Chairman of Obstetrics and Gynecology at University of Tennessee Memphis (1986-1994), Professor and Chairman of Obstetrics and Gynecology at Baylor College of Medicine (1994-2006), and Professor and Founding Executive Associate Dean for Academic Affairs at Florida International University, College of Medicine (2007-2011). He served as Senior Vice President for Research and Global programs, March of Dimes, (MOD) (2012-2018). He remained Professor of Human and Molecular Genetics/ Professor of Obstetrics and Gynecology at Florida International University throughout time at March of Dimes.
During the time he was on leave of absence from FIU, Dr. Simpson oversaw the MOD programs for conference support and individual investigator proposals. He developed a $60M program involving six prematurity research centers dedicated to discovering the causes of labor and, hence, preterm labor. Each center was chosen for its prowess in a given domain of discovery research and its ability to pursue collaborative investigations with other centers. Major discoveries have been made in genes associated with preterm birth, microbiome, fetal gene expression patterns during gestation, gene regulation and uterine pace-marker functions.
Dr. Simpson has contributed to many aspects of reproductive genetics, prenatal genetic diagnosis and birth defects. He is certified in Medical Genetics as well as in Obstetrics and Gynecology. He has written over 800 articles and chapters. His major books include seven editions as co-editor of Obstetrics: Normal and Problem Pregnancies and three editions for Genetics in Obstetrics and Gynecology. He has received research funding from NICHD, March of Dimes, USAID, and the Department of Defense.
Dr. Simpson has served in leadership roles for numerous grant review panels, prestigious national and international committees and many professional organizations. He has been President of the American Society for Reproductive Medicine, International Society of Prenatal Diagnosis, and Society for Gynecologic Investigation, American College of Medical Genetics, and Preimplantation Genetic Diagnosis International Society. He has been a member of the National Academy of Medicine, U.S. National Academy of Sciences since 1994.
He is active in many global initiations, especially in organizations in official relations with World Health Organization. As immediate Past President of the International Federation of Fertility Societies (IFFS), Dr. Simpson is Chair of the Scientific Committee for the 23rd IFFS World Congress (Shanghai, April 11-14, 2019)
research interests
- Prenatal genetic diagnosis, cytogenetics and reproductive genetics
Scholarly & Creative Works
selected publications
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Article
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2021FIGO good practice recommendations on delayed umbilical cord clampingFull Text via DOI: 10.1002/ijgo.13841
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2021FIGO good practice recommendations on progestogens for prevention of preterm deliveryFull Text via DOI: 10.1002/ijgo.13852 Web of Science: 000695639800006
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2021Developing a core outcome set for future infertility research: an international consensus development studyFull Text via DOI: 10.1016/j.fertnstert.2020.11.012 Web of Science: 000607624200038
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2020Developing a core outcome set for future infertility research: an international consensus development studyFull Text via DOI: 10.1093/humrep/deaa241 Web of Science: 000606693900010
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2019Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGDFull Text via DOI: 10.1002/pd.5442 Web of Science: 000466098600003
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2019Good clinical practice advice: Antenatal corticosteroids for fetal lung maturationFull Text via DOI: 10.1002/ijgo.12746
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2019Good clinical practice advice: Iron deficiency anemia in pregnancyFull Text via DOI: 10.1002/ijgo.12740
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2019Good clinical practice advice: Management of twin pregnancyFull Text via DOI: 10.1002/ijgo.12742
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2019Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future DirectionFull Text via DOI: 10.1007/978-1-4939-8889-1_2 Web of Science: 000683214200003
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2017The International Glossary on Infertility and Fertility Care, 2017Full Text via DOI: 10.1016/j.fertnstert.2017.06.005
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2017The international glossary on infertility and fertility care, 2017Full Text via DOI: 10.1093/humrep/dex234
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2017Genetics of Premature Ovarian Failure: New Developments in EtiologyFull Text via DOI: 10.1159/000477276
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2015Chromosome territory repositioning induced by PHA-activation of lymphocytes: A 2D and 3D appraisalFull Text via DOI: 10.1186/s13039-015-0146-3 Web of Science: 000357252900001
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2015CSB-PGBD3 Mutations Cause Premature Ovarian FailureFull Text via DOI: 10.1371/journal.pgen.1005419
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2015Transcription factor SOHLH1 potentially associated with primary ovarian insufficiencyFull Text via DOI: 10.1016/j.fertnstert.2014.11.011 Web of Science: 000348966700040
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2014FMR1 Premutation Is an Uncommon Explanation for Premature Ovarian Failure in Han ChineseFull Text via DOI: 10.1371/journal.pone.0103316 Web of Science: 000339551100103
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2014Novel variants in the SOHLH2 gene are implicated in human premature ovarian failureFull Text via DOI: 10.1016/j.fertnstert.2014.01.001 Web of Science: 000333805000045
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2014Genetics of Female Infertility Due to Anomalies of the Ovary and Mullerian DuctsFull Text via DOI: 10.1007/978-1-4939-0659-8_3 Web of Science: 000338440200004
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2013I1 Clinical challenges in application of prenatal technologiesFull Text via DOI: 10.1016/s1472-6483(13)00237-x
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2012Chromosomal Microarray versus Karyotyping for Prenatal DiagnosisFull Text via DOI: 10.1056/NEJMoa1203382 Web of Science: 000311890600004
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2012Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophyFull Text via DOI: 10.1016/j.rbmo.2012.08.002 Web of Science: 000310639600011
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2012Genetic Causes of Premature Ovarian Failure (POF).Full Text via DOI: 10.1093/biolreprod/87.s1.130
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2012Cytogenetic analysis of 531 Chinese women with premature ovarian failureFull Text via DOI: 10.1093/humrep/des104 Web of Science: 000305458800035
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2012Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trialFull Text via DOI: 10.1002/pd.3863 Web of Science: 000302149400014
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2012Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF)Full Text via DOI: 10.1093/hmg/ddr462 Web of Science: 000298658300016
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2012Invasive procedures for prenatal diagnosis: Any future left?Full Text via DOI: 10.1016/j.bpobgyn.2012.05.007
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2012Xq;autosome translocation in POF: Xq27.2 deletion resulting in haploinsufficiency for SPANXFull Text via DOI: 10.1007/s10815-011-9653-2 Web of Science: 000298999200010
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2011Novel Non-invasive Prenatal Diagnosis as Related to Congenital Adrenal HyperplasiaFull Text via DOI: 10.1007/978-1-4419-8002-1_8 Web of Science: 000321936100008
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2010Moral attitudes and beliefs among couples pursuing PGD for sex selectionFull Text via DOI: 10.1016/j.rbmo.2010.09.009 Web of Science: 000286161400004
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2010C39 PGD and ethics: What limits should be assigned to the indications?Full Text via DOI: 10.1016/s1472-6483(10)62293-6
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2010Plasma cell-free DNA in ovarian cancer: An independent prognostic biomarkerFull Text via DOI: 10.1002/cncr.24997
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2010Florida International University Herbert Wertheim College of MedicineFull Text via DOI: 10.1097/ACM.0b013e3181e86d75
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2009Florida International University: Development and Accreditation of Miami's Public College of MedicineFull Text via DOI: 10.1097/ACM.0b013e3181b6c537 Web of Science: 000207786100034
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2009Mutation analysis of NOBOX homeodomain in chinese women with premature ovarian failureFull Text via DOI: 10.1016/j.fertnstert.2008.08.020 Web of Science: 000265132600063
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2009Impact of PGD on genetic practice and assisted reproductionFull Text via DOI: 10.1016/s1472-6483(10)61196-0
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2008What next for preimplantation genetic screening? Randomized clinical trial in assessing PGS: necessary but not sufficientFull Text via DOI: 10.1093/humrep/den250 Web of Science: 000259327300002
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2008Transcription factor FIGLA is mutated in patients with Premature Ovarian FailureFull Text via DOI: 10.1016/j.ajhg.2008.04.018 Web of Science: 000256647000011
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2008Genetic and phenotypic heterogeneity in ovarian failure - Overview of selected candidate genesFull Text via DOI: 10.1196/annals.1429.019 Web of Science: 000257452900019
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2008Gonadal Dysgenesis in 46,XY Females (XY Gender-Reversal)Full Text via DOI: 10.3843/glowm.10356
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2008PND or PGD: the place of PGD in human medicineFull Text via DOI: 10.1016/s1472-6483(10)61311-9
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2008XX Gonadal Dysgenesis and Premature Ovarian Failure in 46,XX IndividualsFull Text via DOI: 10.3843/glowm.10355
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2007NOBOX homeobox mutation causes premature ovarian failureFull Text via DOI: 10.1086/519496 Web of Science: 000249128200013
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2006Genética del síndrome de ovarios poliquísticosFull Text via DOI: 10.1016/s1283-081x(06)46490-0
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2006Génétique du syndrome des ovaires polykystiquesFull Text via DOI: 10.1016/s0246-1064(06)45020-9
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2005O▪64 Celebrating or restricting the new technology? OverviewFull Text via DOI: 10.1016/s1472-6483(11)60285-x
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2005Research agenda for preterm birth: Recommendations from the March of DimesFull Text via DOI: 10.1016/j.ajog.2005.02.106
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2004Over a decade of experience with preimplantation genetic diagnosis: a multicenter reportFull Text via DOI: 10.1016/j.fertnstert.2003.09.082 Web of Science: 000223263000003
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2004First-Trimester Screening for Trisomies 21 and 18Full Text via DOI: 10.1097/01.ogx.0000115850.05556.bc
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2003Intact fetal cells in maternal plasma: Are they really there?Full Text via DOI: 10.1016/S0140-6736(03)12191-5
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2002Molecular approach to common causes of female infertilityFull Text via DOI: 10.1053/beog.2002.0317
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2002O-2. PGD as part of pre-pregnancy genetic screeningFull Text via DOI: 10.1016/s1472-6483(12)60021-2
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2002Prenatal diagnosis of chromosomal abnormalities using maternal blood.Full Text via DOI: 10.1385/1-59259-300-3:243
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2001Changing indications for preimplantation genetic diagnosis (PGD)Full Text via DOI: 10.1016/S0303-7207(01)00573-1
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1999Evaluation of chorionic villus sampling safetyWeb of Science: 000079100200001
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1998Unintended pregnancies in women delivering at 18 South American hospitalsFull Text via DOI: 10.1093/humrep/13.7.1991
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1996Genetics of male pseudohermaphroditism and true hermaphroditismFull Text via DOI: 10.1016/S1067-5701(96)80008-8
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1996Assessing congenital anomalies after preimplantation genetic diagnosisFull Text via DOI: 10.1007/BF02072540
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1996Chorionic villus sampling safety - Report of World Health Organization EURO meeting in association with the seventh international conference on early prenatal diagnosis of genetic diseases, Tel-Aviv, Israel, May 21, 1994Full Text via DOI: 10.1016/S0002-9378(96)70304-6 Web of Science: A1996UC86600002
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1996Registration of congenital anomalies in ART populations: PitfallsFull Text via DOI: 10.1093/humrep/11.suppl_4.81
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1995Detection of low‐grade mosaicism in fetal cells isolated from maternal bloodFull Text via DOI: 10.1002/pd.1970151218
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1994Lack of heritability in ovarian germ cell malignanciesFull Text via DOI: 10.1016/s0002-9378(12)91850-5
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1994PREIMPLANTATION DIAGNOSIS OF GENETIC AND CHROMOSOMAL DISORDERSFull Text via DOI: 10.1007/BF02214343 Web of Science: A1994PZ51500002
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1994Are obese women at higher risk for producing malformed offspring?Full Text via DOI: 10.1016/S0002-9378(94)70224-1
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1994Fetal Cells in Maternal Blood: Overview and Historical PerspectiveFull Text via DOI: 10.1111/j.1749-6632.1994.tb55743.x
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1994Isolating fetal cells in maternal circulation for prenatal diagnosisFull Text via DOI: 10.1002/pd.1970141308
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1994Lack of heritability in ovarian germ cell malignanciesFull Text via DOI: 10.1016/S0002-9378(94)70356-6
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1993CURRENT PROGRESS IN PREIMPLANTATION GENETIC DIAGNOSISFull Text via DOI: 10.1007/BF01213430 Web of Science: A1993ND15600004
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1993RISK-EVALUATION OF CVSFull Text via DOI: 10.1002/pd.1970130307 Web of Science: A1993KU67100006
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1992Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisFull Text via DOI: 10.1007/BF00220087
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1992Cytogenetic results from the U.S. collaborative study on CVSFull Text via DOI: 10.1002/pd.1970120503
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1992Transvaginal chorionic villus sampling using transabdominal ultrasound guidanceFull Text via DOI: 10.1002/pd.1970120313
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1991Resource management: Opportunities and challengesFull Text via DOI: 10.1016/s0957-5839(06)80063-1
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19919 Screening for fetal and genetic abnormalitiesFull Text via DOI: 10.1016/S0950-3552(05)80264-0
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1990Spermicides, hormonal contraception and congenital malformationsFull Text via DOI: 10.1007/BF01849490
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1989Transabdominal Chorionic Villus Sampling in a Patient with a Bicornuate UterusFull Text via DOI: 10.1055/s-2007-999596
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1988Prenatal Effects of Maternal-Fetal HLA CompatibilityFull Text via DOI: 10.1097/00006254-198843060-00015
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1988Growth disadvantage of 45,X and 46,X,del (X) (p11) fibroblastsFull Text via DOI: 10.1111/j.1399-0004.1988.tb03449.x
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1988Prenatal effects of maternal-fetal HLA compatibilityFull Text via DOI: 10.1097/00006254-198806000-00015
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1987Low fetal loss rates after ultrasound-proved viability in early pregnancyFull Text via DOI: 10.1001/jama.258.18.2555
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1987Fibrinopeptide a increases after Chorionic villus samplingFull Text via DOI: 10.1002/pd.1970070805
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1987Low maternal serum α-fetoprotein and perinatal outcomeFull Text via DOI: 10.1016/0002-9378(87)90341-3
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1987Verification of Early Pregnancy Tests in a Multicenter TrialFull Text via DOI: 10.3181/00379727-184-42468
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1987Verification of early pregnancy tests in a multicenter trial (42468)Full Text via DOI: 10.1097/00006254-198709000-00006
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1986Chorionic villus sampling: First trimester prenatal diagnosisFull Text via DOI: 10.1007/BF02748570
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1986Hypermodal cells, hypomodal cells, and repetitive abortionsFull Text via DOI: 10.1016/s0015-0282(16)49637-8
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1985Genes and chromosomes that cause female infertilityFull Text via DOI: 10.1016/s0015-0282(16)49029-1
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1984Elevated alpha-fetoprotein and acetylcholinesterase associated with hydroceleFull Text via DOI: 10.1002/ajmg.1320190404
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1984Sister chromatid exchanges after exposure to ultrasound and mitomycin CFull Text via DOI: 10.1016/0002-9378(84)90542-8
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1983Genetic Forms of Gonadal Dysgenesis in 46,XX and 46,XY IndividualsFull Text via DOI: 10.1055/s-2007-1022579
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1983Linkage analysis in von Willebrand diseaseFull Text via DOI: 10.1111/j.1399-0004.1983.tb00099.x
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1982Failure to detect polycystic kidneys in utero by second trimester ultrasonographyFull Text via DOI: 10.1007/BF00303026
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1981Ultrasonic induction of sister chromatid exchanges in human lymphocytesFull Text via DOI: 10.1007/BF00283668
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1981Chromosome analysis of ectopic human conceptusesFull Text via DOI: 10.1016/s0002-9378(15)33314-7
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1980Clinical Genetics: A Source Book for PhysiciansFull Text via DOI: 10.1001/jama.1980.03310010063038
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1980Heritable aspects of endometriosis. I. Genetic studiesFull Text via DOI: 10.1016/0002-9378(80)90917-5
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1980Pericentric X chromosome ascertained during antenatal diagnosisFull Text via DOI: 10.1111/j.1399-0004.1980.tb01361.x
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1980Prenatal diagnosis of harlequin ichthyosisFull Text via DOI: 10.1111/j.1399-0004.1980.tb00147.x
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1979Genetically determined sex-reversal in 46, XY humansFull Text via DOI: 10.1097/00006254-197903000-00019
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1977Diagnosis and management of the infant with genital ambiguityFull Text via DOI: 10.1016/0002-9378(77)90677-9
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1976Genetics for the obstetrician gynecologist: Questions and answersFull Text via DOI: 10.1097/00003081-197612000-00023
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1976Prenatal diagnosis of cytogenetic disordersFull Text via DOI: 10.1097/00003081-197612000-00013
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1969Gonadal dysgenesis as an autosomal recessive conditionFull Text via DOI: 10.1016/0002-9378(69)90697-8
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Book
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2016Obstetrics: Normal and Problem PregnanciesFull Text via DOI: 10.1016/B978-0-323-32108-2.00063-9
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2013
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2011Preface. Ed. 707.
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Book Chapter
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2022The Genetic Risk of a Couple Aiming to Conceive. 24-35.Full Text via DOI: 10.1201/9781003024941-3
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20225 Hypogonadotropic and Hypergonadotropic Hypogonadism in Females: Disorders of Reproductive Ducts. 87-119.Full Text via DOI: 10.1016/b978-0-12-815236-2.00005-9
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2020Preimplantation Genetic Testing in the Future. 151-156.Full Text via DOI: 10.1201/9780429445972-11
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2019Chapter 28 Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders. 461-484.Full Text via DOI: 10.1016/b978-0-12-813209-8.00028-5
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2019Chapter 29 Prenatal Diagnosis and Treatment of Genetic Steroid Disorders. 653-658.Full Text via DOI: 10.1016/b978-0-12-813570-9.00029-2
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2019Prenatal Diagnosis and Treatment of Genetic Steroid Disorders. 653-658.Full Text via DOI: 10.1016/B978-0-12-813570-9.00029-2 Web of Science: 000534279800029
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2016Early Pregnancy Loss and Stillbirth. 578-594.Full Text via DOI: 10.1016/B978-0-323-32108-2.00027-5
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2016Genetic Screening and Prenatal Genetic Diagnosis. 193-218.Full Text via DOI: 10.1016/B978-0-323-32108-2.00010-X
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2015Preimplantation genetic screening and diagnostic testing. 31-47.Full Text via DOI: 10.1007/978-3-319-18911-6_2
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2014Chapter 13C Preimplantation Diagnosis and Other Modern Methods for Prenatal Diagnosis. 343-350.Full Text via DOI: 10.1016/b978-0-12-416006-4.00028-4
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2014Disorders of the Gonads, Genital Tract, and GenitaliaFull Text via DOI: 10.1016/b978-0-12-801238-3.05560-4
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2014Preimplantation Diagnosis and Other Modern Methods for Prenatal Diagnosis. 343-350.Full Text via DOI: 10.1016/B978-0-12-416006-4.00028-4
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2013Disorders of the gonads, genital tract, and genitalia. 1-45.Full Text via DOI: 10.1016/B978-0-12-383834-6.00092-6
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2013Chapter 88 Disorders of the Gonads, Genital Tract, and Genitalia. 1-45.Full Text via DOI: 10.1016/b978-0-12-383834-6.00092-6
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2012Chapter 10 Genetic Counseling and Genetic Screening. 193-209.Full Text via DOI: 10.1016/b978-1-4377-1935-2.00010-7
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2012Chapter 11 Prenatal Genetic Diagnosis. 210-236.Full Text via DOI: 10.1016/b978-1-4377-1935-2.00011-9
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2012Chapter 8 Drugs and Environmental Agents in Pregnancy and Lactation Embryology, Teratology, Epidemiology. 140-165.e4.Full Text via DOI: 10.1016/b978-1-4377-1935-2.00008-9
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2008Principles of Human Genetics: Chromosomal and Single-Gene Disorders. 110-116.Full Text via DOI: 10.1002/9780470753323.ch18
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2008Principles of Human Genetics: Chromosomal and Singlegene Disorders. 293-317.Full Text via DOI: 10.1002/9780470753293.ch20
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2007CHAPTER 6 Genetic Counseling and Genetic Screening. 138-151.Full Text via DOI: 10.1016/b978-0-443-06930-7.50008-6
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2007CHAPTER 7 Prenatal Genetic Diagnosis. 152-183.Full Text via DOI: 10.1016/b978-0-443-06930-7.50009-8
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2007CHAPTER 8 Drugs and Environmental Agents in Pregnancy and Lactation: Embryology, Teratology, Epidemiology. 184-214.Full Text via DOI: 10.1016/b978-0-443-06930-7.50010-4
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2007Chapter 3 Genetic programming in ovarian development and oogenesis. 29-47.Full Text via DOI: 10.1016/b978-012369443-0/50005-3
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2007
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2006Intact Fetal Cells and Cell-free DNA in Maternal Blood:. 314-314.Full Text via DOI: 10.5005/jp/books/10670_16
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2004Chapter 32 Germ Cell Failure and Ovarian Resistance Human Genes and Disorders. 541-557.Full Text via DOI: 10.1016/b978-012444562-8/50033-1
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2004Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders. 541-557.Full Text via DOI: 10.1016/B978-012444562-8/50033-1
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2002Prenatal Diagnosis of Chromosomal Abnormalities Using Maternal Blood. 243-258.Full Text via DOI: 10.1385/1-59259-300-3:243
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2000Chapter 5 Genetic Programming in Ovarian Development and Oogenesis. 77-94.Full Text via DOI: 10.1016/b978-012453790-3/50006-8
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199413 XY Sex Reversal in the Human. 287-309.Full Text via DOI: 10.1016/b978-0-12-728960-1.50017-3
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1993Prenatal Diagnosis of Genetic Disorders. 172-202.Full Text via DOI: 10.1007/978-1-4613-9240-8_10
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1991Assessing Loss Rates in the Preimplantation Stages of Gestation. 175-180.Full Text via DOI: 10.1007/978-1-4684-1351-9_19
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1989Evaluation and Development of a System for Automated Preparation of Blood Specimens for Cytogenetic Analysis. 149-173.Full Text via DOI: 10.1007/978-3-642-74738-0_13
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1987Ovarian Dysgenesis and Related Genetic Disorders. 303-326.Full Text via DOI: 10.1007/978-1-4613-2157-6_14
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1987Phenotypic-Karyotypic Correlations of Gonadal Determinants: Current Status and Relationship to Molecular Studies. 224-232.Full Text via DOI: 10.1007/978-3-642-71635-5_27
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1985Methodological Problems in Determining Fetal Loss Rates: Relevance to Chorionic Villi Sampling. 321-333.Full Text via DOI: 10.1007/978-3-642-70707-0_50
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Conference
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2017Risky Business: Meeting the Structural Needs of Transdisciplinary Science. 255-258.Full Text via DOI: 10.1016/j.jpeds.2017.08.072
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2013Novel Variants in the H1FOO Gene Are Associated with Premature Ovarian Failure. 170A-170A.Web of Science: 000329543100367
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2013Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status. 1124-1134.Full Text via DOI: 10.1016/j.fertnstert.2013.02.012
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2006Hypoxia-induced membrane-bound apoptotic DNA particles: Potential mechanism of fetal DNA in maternal plasma. 57-62.Full Text via DOI: 10.1196/annals.1368.007
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2006Quantification of total plasma cell-free DNA in ovarian cancer using real-time PCR. 230-234.Full Text via DOI: 10.1196/annals.1368.031
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2002Heritability and molecular genetic studies of endometriosis. 239-251.Full Text via DOI: 10.1111/j.1749-6632.2002.tb02785.x
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1999
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1999Increased heterogeneity of chromosome 17 aneuploidy in endometriosis. 792-797.Full Text via DOI: 10.1016/S0002-9378(99)70649-6
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1998The Society for Gynecologic Investigation as a year-round society. 287.Full Text via DOI: 10.1016/S1071-5576(98)00036-7
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1997Effects of timing of conception on birth weight and preterm delivery of natural family planning users. 215-228.Full Text via DOI: 10.1023/A:1006508106197
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1997Pregnancy complications in natural family planning users. 229-237.Full Text via DOI: 10.1023/A:1006560123036
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1997Pregnancy outcome in natural family planning users: Cohort and case-control studies evaluating safety. 201-214.Full Text via DOI: 10.1023/A:1006556022127
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1994
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1992Marker chromosomes in gonadal dysgenesis: Avoiding unnecessary surgery. 39-42.Full Text via DOI: 10.1016/S0932-8610(12)80105-8
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1986Chorionic villus sampling in continuing pregnancies I. Low fetal loss rates in initial 109 cases. 1349-1352.Full Text via DOI: 10.1016/0002-9378(86)90723-4
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1986Chorionic villus sampling in continuing pregnancies II. Cytogenetic reliability. 1353-1362.Full Text via DOI: 10.1016/0002-9378(86)90724-6
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Editorial Material
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2019PGDIS Position Statement on the Transfer of Mosaic Embryos 2019. e1-e4.Full Text via DOI: 10.1016/j.rbmo.2019.06.012
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2017First birth following spindle transfer for mitochondrial replacement therapy: hope and trepidation. 333-336.Full Text via DOI: 10.1016/j.rbmo.2017.02.004
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2014Telomere length and aneuploidy: Clinical and biological insights into human preimplantation embryos. 531-532.Full Text via DOI: 10.1016/j.rbmo.2014.03.009
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2010Are we ready for universal genetic screening?. 437-439.Full Text via DOI: 10.1016/j.rbmo.2010.07.002
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2005Choosing the best prenatal screening protocol. 2068-2070.Full Text via DOI: 10.1056/NEJMe058189
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2005Where are the genes that cause endometriosis?. 143-144.Full Text via DOI: 10.1016/j.jsgi.2005.02.001
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2004Cell-Free Fetal DNA in Maternal Blood: Evolving Clinical Applications. 1135-1137.Full Text via DOI: 10.1001/jama.291.9.1135
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2003Public objections to designer babies and cloning in USA: Not quite what was expected. 147-148.Full Text via DOI: 10.1016/S1472-6483(10)61699-9
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2001Genetics of common disorders causing female infertility: Part I. 2.Full Text via DOI: 10.1093/humupd/7.1.2
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1999Disorders of sexual differentiation. 175.Full Text via DOI: 10.1002/(SICI)1096-8628(19991229)89:4<175::AID-AJMG1>3.0.CO;2-F
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1999Fetal surgery for myelomeningocele: Promise, progress, and problems. 1873-1874.Full Text via DOI: 10.1001/jama.282.19.1873
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1996Reproductive medicine in a shrinking world. 248-249.Full Text via DOI: 10.1016/S0015-0282(16)58078-9
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1995Pregnancy and the timing of intercourse. 1563-1565.Full Text via DOI: 10.1056/NEJM199512073332311
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1987
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1981Genetic screening for donors in artificial insemination. 395-402.Full Text via DOI: 10.1016/s0015-0282(16)45430-0
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1979More Than We Ever Wanted to Know about Sex — Should We Be Afraid to Ask?. 1483-1484.Full Text via DOI: 10.1056/NEJM197906283002609
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1979
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Letter
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2017Response from the Editors: First birth following spindle transfer. 548.Full Text via DOI: 10.1016/j.rbmo.2017.07.002
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2011Genetic factors in stillbirths. 878-878.Full Text via DOI: 10.1016/S0140-6736(11)61416-5 Web of Science: 000294791300027
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2010The Illusory "Level Playing Field". 4-5.Web of Science: 000284395000004
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2007In vitro fertilization with preimplantation genetic screening. 1769-1770.Web of Science: 000250355100017
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1999Fetal cells in maternal blood: NIFTY clinical trial interim analysis [2]. 994-995.Full Text via DOI: 10.1002/(SICI)1097-0223(199910)19:10<994::AID-PD662>3.0.CO;2-H
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1998Low false-positive rate of aneuploidy detection using fetal cells isolated from maternal blood [1]. 380.Full Text via DOI: 10.1159/000020874
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1996Fetoscopy, fetal-tissue sampling and the ESHRE guidelines on prenatal diagnosis.. 682.Full Text via DOI: 10.1093/HUMREP/11.3.682
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1996Pregnancy and the timing of intercourse [1]. 1266-1268.Full Text via DOI: 10.1056/NEJM199605093341911
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1995Down syndrome is not increased in offspring of natural family planning users (case control analysis). 525.Full Text via DOI: 10.1002/ajmg.1320590424
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1995Prenatal diagnosis by use of fetal cells isolated from maternal blood. 1354-1355.Full Text via DOI: 10.1016/0002-9378(95)91393-9
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1993In Reply: Caffeine Use During Pregnancy: How Much Is Safe?. 47-48.Full Text via DOI: 10.1001/jama.1993.03510010052026
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1992First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood.. 1033.Full Text via DOI: 10.1016/0140-6736(92)93041-k
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1992Early twin amniocentesis prior to 14 weeks' gestation. 625-626.Full Text via DOI: 10.1002/pd.1970120710
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1991Maternal serum alpha-fetoprotein screening in adolescents. 51.Full Text via DOI: 10.1016/S0932-8610(12)80095-8
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1991Minimal fetomaternal transfusion in ultrasound‐guided fetal skin sampling. 924-927.Full Text via DOI: 10.1002/pd.1970111210
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1990Second trimester maternal serum human chorionic gonadotropin and unconjugated oestriol levels in blacks and whites. 1459-1460.Full Text via DOI: 10.1016/0140-6736(90)91485-S
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1990Vitamins During Pregnancy and Neural Tube Defects. 2747-2748.Full Text via DOI: 10.1001/jama.1990.03440200049013
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1990Periconceptional Use of Multivitamins and the Prevalence of Neural-Tube Defects. 1082-1084.Full Text via DOI: 10.1056/NEJM199004123221513
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1989Dilatation and evacuation is a preferable method of mid‐trimester genetic termination of pregency. 741-742.Full Text via DOI: 10.1002/pd.1970091010
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1988Diabetic Control and Fetal Malformations. 647-649.Full Text via DOI: 10.1056/NEJM198809083191011
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1986
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1985Prenatal Diagnosis of Congenital Muscular Dystrophy Producing Arthrogryposis. 1230.Full Text via DOI: 10.1056/NEJM198511073131918
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1985Increased male-to-female sex ratio among HLA-DR compatible pregnancies.. 761.Full Text via DOI: 10.1016/s0140-6736(85)91307-8
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1983Further comments on amniocentesis in twin gestations. 397-398.Full Text via DOI: 10.1002/ajmg.1320140223
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1980Amniocentesis for prenatal diagnosis in twin gestation.. 300-301.Full Text via DOI: 10.1111/j.1399-0004.1980.tb00152.x
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1978Intrauterine Growth Retardation in Osteogenesis Imperfecta. 23.Full Text via DOI: 10.1001/jama.1978.03280280023006
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1977Delayed Fertilization and Down's Syndrome. 1811.Full Text via DOI: 10.1001/jama.1977.03280180015006
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1973CYTOGENETIC CONFIRMATION OF FAILURE OF POLAR-BODY EXTRUSION. 1391-1392.Full Text via DOI: 10.1016/S0140-6736(73)93363-1
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1973TESTICULAR FEMINISATION AND INGUINAL HERNIA. 891.Full Text via DOI: 10.1016/S0140-6736(73)91467-0
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1972Chromosomal mosaicism. 768-769.
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Note
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2013Chromosomal microarray versus karyotyping for prenatal diagnosis. 276-278.Full Text via DOI: 10.1097/01.ogx.0000429294.57890.b8
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2003Toward scientific discussion of human reproductive cloning. 10-11.Full Text via DOI: 10.1016/S1472-6483(10)61721-X
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2001Celebrating preimplantation genetic diagnosis of p53 mutations in Li-Fraumeni syndrome. 2-3.Full Text via DOI: 10.1016/S1472-6483(10)61953-0
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1996Multifetal reduction in high-order gestations: a nonelective procedure?. 1-2.Full Text via DOI: 10.1177/107155769600300101
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Other Scholarly Work
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2021FIGO good practice recommendations for reducing preterm birth and improving child outcomes. 1-4.Full Text via DOI: 10.1002/ijgo.13863 Web of Science: 000695639800001
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2020Preterm birth: A clinical enigma and a worldwide public health concern. 1-2.Full Text via DOI: 10.1002/ijgo.13194 Web of Science: 000539273000001
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2019Before the beginning: the genetic risk of a couple aiming to conceive. 622-630.Full Text via DOI: 10.1016/j.fertnstert.2019.08.002 Web of Science: 000487818300003
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2019Can Pregnancies Be Achieved in Premature Ovarian Insufficiency?. 157-158.Full Text via DOI: 10.1177/1933719118823597 Web of Science: 000459609700001
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2017Why are we still talking about chromosomal heteromorphisms?. 1-2.Full Text via DOI: 10.1016/j.rbmo.2017.05.006 Web of Science: 000407005000002
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2016The Olympic Games and Athletic Sex Assignment. 1359-1360.Full Text via DOI: 10.1001/jama.2016.11850 Web of Science: 000384591300013
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2016Commentary re: Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy. 585-586.Full Text via DOI: 10.1016/j.rbmo.2016.08.018 Web of Science: 000386591100007
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2015Improving assisted reproductive technology pregnancy rates: excluding aneuploid and interrogating euploid embryos. 557-558.Full Text via DOI: 10.1016/j.fertnstert.2015.06.017 Web of Science: 000366484100014
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2013Next-generation sequencing for preimplantation genetic diagnosis. 1203-1204.Full Text via DOI: 10.1016/j.fertnstert.2013.01.112 Web of Science: 000317393700015
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2012NON-SYNONYMOUS SINGLE NUCLEOTIDE POLYMORPHISM IN MCM8 DECREASED IN A COHORT OF PREMATURE OVARIAN FAILURE PATIENTS. S208-S208.Full Text via DOI: 10.1016/j.fertnstert.2012.07.1083 Web of Science: 000209842700689
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2012Is Cell-Free Fetal DNA From Maternal Blood Finally Ready for Prime Time?. 883-885.Full Text via DOI: 10.1097/AOG.0b013e318251e499 Web of Science: 000303150000001
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2011Salute to a giant ... Robert Geoffrey Edwards. 1-98.Web of Science: 000303047900001
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2011Fetal Surgery for Myelomeningocele?. 1076-1077.Full Text via DOI: 10.1056/NEJMe1101228 Web of Science: 000288439000014
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2010SEX AND GENDER IN SPORT: FALLACY OF THE "LEVEL PLAYING FIELD". 149-149.Full Text via DOI: 10.1203/00006450-201011001-00289 Web of Science: 000208479700290
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2010Preface: Genetic Screening and Counseling. XV-XVI.Full Text via DOI: 10.1016/j.ogc.2010.04.001 Web of Science: 000278966600002
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2010Children born after preimplantation genetic diagnosis show no increase in congenital anomalies. 6-8.Full Text via DOI: 10.1093/humrep/dep428 Web of Science: 000272929600003
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2009Yury Verlinsky (01/09/1943-16/07/2009): pioneer in CVS, PGD and hESC Obituary. 298-299.Full Text via DOI: 10.1016/S1472-6483(10)60162-9 Web of Science: 000269966400003
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2008Developing a national collaborative study system for rare genetic diseases. 325-329.Full Text via DOI: 10.1097/GIM.0b013e31817b80fd Web of Science: 000256069800004
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2008Analysis of LHX8 mutation in premature ovarian failure. 1012-1014.Full Text via DOI: 10.1016/j.fertnstert.2007.04.017 Web of Science: 000255250100041
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2007Substandard application screening may interfere of preimplantation genetic with its clinical success. 781-784.Full Text via DOI: 10.1016/j.fertnstert.2007.08.002 Web of Science: 000250192800003
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2005Genetic testing of embryos: a critical need for data. 667-670.Full Text via DOI: 10.1016/S1472-6483(10)61681-1 Web of Science: 000233857100004
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2004Protein expression profiling of endometriosis: validation of 2-mm tissue microarrays. 1681-1683.Full Text via DOI: 10.1016/j.fertnstert.2004.06.044 Web of Science: 000225802300034
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2004Over a decade of experience with preimplantation genetic diagnosis. 302-303.Full Text via DOI: 10.1016/j.fertnstert.2004.02.108 Web of Science: 000223263000007
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1999Bowel and mesenteric injury: evaluation with emergency abdominal US.. 399-403.Full Text via DOI: 10.1148/radiology.211.2.r99ma54399
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1997Current status of preimplantation diagnosis. 72-75.Full Text via DOI: 10.1007/BF02765773 Web of Science: A1997WH84000002
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1995Isolating fetal cells in the maternal circulation.. 409-418.Full Text via DOI: 10.1093/humupd/1.4.409
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1975A patient with the Larsen syndrome.. 116-120.
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Review
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2022PGDIS position statement on the transfer of mosaic embryos 2021.. 19-25.Full Text via DOI: 10.1016/j.rbmo.2022.03.013
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2020Preimplantation genetic testing to reduce preterm births in assisted reproductive technology. 34-40.Full Text via DOI: 10.1002/ijgo.13192 Web of Science: 000539273000007
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2019Prenatal genetic testing and treatment for congenital adrenal hyperplasia. 21-23.Full Text via DOI: 10.1016/j.fertnstert.2018.11.041 Web of Science: 000454711800004
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2018Forty years of IVF. 185-+.Full Text via DOI: 10.1016/j.fertnstert.2018.06.005 Web of Science: 000439966800001
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2017Preimplantation diagnosis and other modern methods for prenatal diagnosis. 124-130.Full Text via DOI: 10.1016/j.jsbmb.2016.03.022 Web of Science: 000390506200017
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2015Genetics of primary ovarian insufficiency: new developments and opportunities. 787-808.Full Text via DOI: 10.1093/humupd/dmv036 Web of Science: 000364766700008
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2015Cell-free DNA versus intact fetal cells for prenatal genetic diagnostics: what does the future hold?. 989-998.Full Text via DOI: 10.1586/14737159.2015.1051529 Web of Science: 000358295300004
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2014Birth defects and assisted reproductive technologies. 177-182.Full Text via DOI: 10.1016/j.siny.2014.01.001
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2013Can microarray analysis reveal additional abnormalities in prenatal diagnosis?. 193-195.Full Text via DOI: 10.1586/eog.13.15
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2011Novel Therapies for Treating Short Stature with Congenital Adrenal Hyperplasia. 45-50.Full Text via DOI: 10.5005/jp-journals-10016-1017
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2010Micronutrients and women of reproductive potential: required dietary intake and consequences of dietary deficiency or excess. Part I - Folate, Vitamin B12, Vitamin B6. 1323-1343.Full Text via DOI: 10.3109/14767051003678234 Web of Science: 000284075000001
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2010Preimplantation genetic diagnosis at 20 years. 682-695.Full Text via DOI: 10.1002/pd.2552 Web of Science: 000279835800017
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2010Role of preimplantation genetic diagnosis (PGD) in current infertility practice. 1-10.Full Text via DOI: 10.5005/jp-journals-10016-1001
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2007The FMR1 premutation and reproduction. 456-465.Full Text via DOI: 10.1016/j.fertnstert.2006.09.004
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2006Endocervical fetal trophoblast for prenatal genetic diagnosis. 216-220.Full Text via DOI: 10.1097/01.gco.0000192985.22718.17
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2005ART and offspring anomalies: How concerned should we be?. 52-58.Full Text via DOI: 10.1016/j.sram.2005.09.008
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2005Cell-free fetal DNA in maternal blood: Kinetics, source and structure. 59-67.Full Text via DOI: 10.1093/humupd/dmh053
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2005Preimplantation genetic diagnosis (PGD) for heritable neoplasia.. 87-90.Full Text via DOI: 10.1093/jncimonographs/lgi027
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2004Genetics of endometriosis: Heritability and candidate genes. 219-232.Full Text via DOI: 10.1016/j.bpobgyn.2004.01.004
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2004The genetics of polycystic ovary syndrome. 707-718.Full Text via DOI: 10.1016/j.bpobgyn.2004.05.002
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2003Klinefelter syndrome: Expanding the phenotype and identifying new research directions. 460-468.Full Text via DOI: 10.1097/01.GIM.0000095626.54201.D0
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2003Heritability and candidate genes for endometriosis. 162-169.Full Text via DOI: 10.1016/S1472-6483(10)61746-4
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2002
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2002Genetic counseling in translocations. 793-807.Full Text via DOI: 10.1016/S0094-0143(02)00088-5
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2002A general approach to genetic counseling. 265-276.Full Text via DOI: 10.1016/S0889-8545(02)00003-7
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2002Genetic screening for cystic fibrosis. 329-340.Full Text via DOI: 10.1016/S0889-8545(02)00005-0
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2001Genetic effects of intracytoplasmic sperm injection. 239-249.Full Text via DOI: 10.1055/s-2001-18043
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2000Genetic factors in common disorders of female infertility. 173-202.Full Text via DOI: 10.1017/S0962279900000314
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2000Gender verification of female athletes. 249-254.Full Text via DOI: 10.1097/00125817-200007000-00008
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2000Heritability and molecular genetic studies of endometriosis. 37-44.Full Text via DOI: 10.1093/humupd/6.1.37
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1999Genetics of the female reproductive ducts. 224-239.Full Text via DOI: 10.1002/(SICI)1096-8628(19991229)89:4<224::AID-AJMG7>3.0.CO;2-C
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1999Ovarian differentiation and gonadal failure. 186-200.Full Text via DOI: 10.1002/(SICI)1096-8628(19991229)89:4<186::AID-AJMG3>3.0.CO;2-5
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1995
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1994Single-cell genetic diagnosis: Molecular methods and pitfalls. 196-200.Full Text via DOI: 10.1055/s-2007-1016400
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1993Gender Verification in Competitive Sports. 305-315.Full Text via DOI: 10.2165/00007256-199316050-00002
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1992The de Watteville Memorial Lecture: reproductive technologies and genetic advances in obstetrics and gynecology.. 261-280.Full Text via DOI: 10.1016/0020-7292(92)91018-j
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1992Preimplantation genetics and recovery of fetal cells from maternal blood. 295-301.Full Text via DOI: 10.1097/00001703-199204000-00016
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1990Chorionic villus sampling. 446-455.
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1990Incidence and timing of pregnancy losses: Relevance to evaluating safety of early prenatal diagnosis. 165-173.Full Text via DOI: 10.1002/ajmg.1320350205
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1989
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1987Abnormal sexual differentiation and neoplasia. 191-218.Full Text via DOI: 10.1016/0165-4608(87)90180-4
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1986Gestational diabetes mellitus: A syndrome with phenotypic and genotypic heterogeneity. 427-430.Full Text via DOI: 10.1055/s-2007-1012338
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1985Relationship between congenital anomalies and contraception. 3-30.Full Text via DOI: 10.1007/BF01849140
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1982Abnormal sexual differentiation in humans.. 193-224.Full Text via DOI: 10.1146/annurev.ge.16.120182.001205
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1982The prenatal diagnosis of genetic disorders. 635-658.Full Text via DOI: 10.1097/00003081-198212000-00004
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1981Antenatal diagnosis of cytogenetic abnormalities. 1023-1039.Full Text via DOI: 10.1097/00003081-198112000-00004
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1981Repeated suboptimal pregnancy outcome.. 113-142.
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1980
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1979
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1978Male pseudohermaphroditism: Genetics and Clinical delineation. 1-49.Full Text via DOI: 10.1007/BF00283573
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1972Genetic aspects of gynecologic disorders occurring in 46,XX individuals.. 157-182.Full Text via DOI: 10.1097/00003081-197203000-00005
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1969Hereditary factors in obstetrics and gynecology. 580-601.Full Text via DOI: 10.1097/00006254-196907000-00002
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Research
principal investigator on
- Mass Scale Biosensor Threat Dianostic for In-Theater Defense Utilization awarded by U.S. Army 2010 - 2013
- Health Care and Other Facilities awarded by Health Resources & Services Administrati 2009 - 2011
Contact
full name
- Joe Simpson
Identifiers
ORCID iD
- https://orcid.org/0000-0002-5309-6881 (confirmed)
visualizations
publication subject areas
- Biochemistry & Molecular Biology
- Biomedical Social Sciences
- Education & Educational Research
- Endocrinology & Metabolism
- General & Internal Medicine
- Genetics & Heredity
- Geriatrics & Gerontology
- Health Care Sciences & Services
- Medical Ethics
- Neurosciences & Neurology
- Obstetrics & Gynecology
- Pathology
- Pediatrics
- Reproductive Biology
- Science & Technology - Other Topics
- Social Sciences - Other Topics