Joe Leigh Simpson

Joe Leigh Simpson's AcademicInfluence.com Rankings

Joe Leigh Simpson

Biology

#6138

World Rank

#8788

Historical Rank

Genetics

#569

World Rank

#648

Historical Rank

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Biology

Joe Leigh Simpson's Degrees

Doctorate Medicine Stanford University

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Joe Leigh Simpson's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Chromosomal microarray versus karyotyping for prenatal diagnosis. (2012) (989)
Obstetrics: Normal and Problem Pregnancies (1986) (981)
The International Glossary on Infertility and Fertility Care, 2017. (2017) (794)
Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index (2012) (505)
The International Glossary on Infertility and Fertility Care, 2017†‡§ (2017) (453)
Heritable aspects of endometriosis. I. Genetic studies. (1980) (435)
Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis (1988) (367)
The FMR1 premutation and reproduction. (2007) (357)
First-trimester screening for trisomies 21 and 18 (2003) (353)
Abnormal sexual differentiation and neoplasia. (1987) (349)
Incidence of spontaneous abortion among normal women and insulin-dependent diabetic women whose pregnancies were identified within 21 days of conception. (1988) (346)
Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data (2002) (337)
Genetics of primary ovarian insufficiency: new developments and opportunities (2015) (334)
Cytogenetic results from the U.S. collaborative study on CVS (1992) (311)
Metabolic Control and Progression of Retinopathy: The Diabetes in Early Pregnancy Study (1995) (301)
Are obese women at higher risk for producing malformed offspring? (1994) (298)
Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancy-associated plasma protein A, and nuchal translucency with intrauterine growth restriction and other adverse pregnancy outcomes. (2004) (243)
Ovarian differentiation and gonadal failure. (1999) (241)
The absence of a relation between the periconceptional use of vitamins and neural-tube defects. National Institute of Child Health and Human Development Neural Tube Defects Study Group. (1989) (230)
Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. (2005) (227)
NOBOX homeobox mutation causes premature ovarian failure. (2007) (221)
Research agenda for preterm birth: recommendations from the March of Dimes. (2005) (215)
Heritability and molecular genetic studies of endometriosis. (2000) (211)
First-trimester screening for trisomies 21 and 18. (2004) (208)
Over a decade of experience with preimplantation genetic diagnosis: a multicenter report. (2004) (202)
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group. (1992) (200)
Isolating fetal cells from maternal blood. Advances in prenatal diagnosis through molecular technology. (1993) (178)
Klinefelter syndrome: Expanding the phenotype and identifying new research directions (2003) (177)
Transcription factor FIGLA is mutated in patients with premature ovarian failure. (2008) (177)
Cell-free fetal DNA in maternal blood: kinetics, source and structure. (2005) (167)
Forty years of IVF. (2018) (165)
Physiological reduction in fasting plasma glucose concentration in the first trimester of normal pregnancy: the diabetes in early pregnancy study. (1998) (161)
Frequency of diabetes mellitus in mothers of probands with gestational diabetes: possible maternal influence on the predisposition to gestational diabetes. (1985) (161)
Maternal Serum Screening for Fetal Down Syndrome in Women Less Than 35 Years of Age Using Alpha-Fetoprotein, hCG, and Unconjugated Estriol: A Prospective 2-Year Study (1992) (154)
Moderate caffeine use and the risk of spontaneous abortion and intrauterine growth retardation (1993) (137)
Cross-Country Individual Participant Analysis of 4.1 Million Singleton Births in 5 Countries with Very High Human Development Index Confirms Known Associations but Provides No Biologic Explanation for 2/3 of All Preterm Births (2016) (136)
Growth differentiating factor-9 mutations may be associated with premature ovarian failure. (2007) (132)
First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood (1992) (129)
Circulating cell-free DNA: A novel biomarker for response to therapy in ovarian carcinoma (2006) (128)
Heritable aspects of endometriosis (1980) (121)
Genetics of the female reproductive ducts. (2000) (119)
Heritage aspects of endometriosis. II. Clinical characteristics of familial endometriosis. (1980) (118)
Micronutrients and women of reproductive potential: required dietary intake and consequences of dietary deficiency or excess. Part I – Folate, Vitamin B12, Vitamin B6 (2010) (115)
Interlaboratory comparison of fetal male DNA detection from common maternal plasma samples by real-time PCR. (2004) (114)
Elevated pregnancy losses at high and low extremes of maternal glucose in early normal and diabetic pregnancy: evidence for a protective adaptation in diabetes. (2005) (110)
Substandard application of preimplantation genetic screening may interfere with its clinical success. (2007) (105)
The Diabetes in Early Pregnancy Study: beta-hydroxybutyrate levels in type 1 diabetic pregnancy compared with normal pregnancy. NICHD-Diabetes in Early Pregnancy Study Group (DIEP). National Institute of Child Health and Development. (1998) (105)
Low fetal loss rates after ultrasound-proved viability in early pregnancy. (1987) (105)
A previously unrecognized X-linked syndrome of dysmorphia. (1975) (105)
Causes of fetal wastage. (2007) (100)
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients. (2001) (98)
Genetics in obstetrics and gynecology (1982) (98)
Late First-Trimester Invasive Prenatal Diagnosis: Results of an International Randomized Trial (2004) (96)
Genes, chromosomes, and reproductive failure. (1980) (96)
Transformations and losses of urea nitrogen after application to flooded rice (1984) (94)
Cytogenetic analysis of 531 Chinese women with premature ovarian failure. (2012) (93)
Parental decision following prenatal diagnosis of fetal chromosome abnormality. (1988) (92)
Declining insulin requirement in the late first trimester of diabetic pregnancy. (2001) (91)
Disorders of sexual differentiation: Etiology and clinical delineation (1976) (91)
Noninvasive Determination of Fetal RhD Status Using Fetal DNA in Maternal Serum and PCR (1999) (90)
Somatic DNA alterations in endometriosis: high frequency of chromosome 17 and p53 loss in late-stage endometriosis. (2002) (88)
PGDIS Position Statement on the Transfer of Mosaic Embryos 2019. (2019) (85)
Shared HLA antigens and reproductive performance among Hutterites. (1983) (84)
Sequential Pathways of Testing After First-Trimester Screening for Trisomy 21 (2004) (83)
Micronutrients and women of reproductive potential: required dietary intake and consequences of dietary deficienty or excess. Part II - Vitamin D, Vitamin A, Iron, Zinc, Iodine, Essential Fatty Acids (2011) (82)
Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy. (2012) (82)
Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure. (2007) (78)
Pregnancy-Associated Plasma Protein A, Free β-hCG, Nuchal Translucency, and Risk of Pregnancy Loss (2004) (78)
Predictive value, sensitivity, and specificity of ultrasonic targeted imaging for fetal anomalies in gravid women at high risk for birth defects. (1985) (77)
Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry. (1996) (76)
Diabetes in pregnancy, Northwestern University series (1977-1981). I. Prospective study of anomalies in offspring of mothers with diabetes mellitus. (1983) (76)
Endometrial adenocarcinoma: genetic analysis suggesting heritable site-specific uterine cancer. (1992) (74)
Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis. (2002) (74)
Genetically determined sex-reversal in 46,XY humans (1978) (74)
Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data. (1971) (73)
Isolated fetal choroid plexus cysts and trisomy 18: a review and meta-analysis. (1995) (73)
Genetic and Phenotypic Heterogeneity in Ovarian Failure (2008) (72)
Increased heterogeneity of chromosome 17 aneuploidy in endometriosis. (1999) (71)
Fetal Cells in the Maternal Circulation: Isolation by Multiparameter Flow Cytometry and Confirmation by Polymerase Chain Reaction (1991) (70)
CSB-PGBD3 Mutations Cause Premature Ovarian Failure (2015) (68)
The genetics of polycystic ovary syndrome. (2004) (68)
Chorionic 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, 1994. (1996) (66)
Genetic amniocentesis in twin gestations. (1980) (66)
Chorionic mosaicism: Association with fetal loss but not with adverse perinatal outcome (1992) (66)
Genetics of endometriosis: heritability and candidate genes. (2004) (65)
Vitamin A and birth defects. (1997) (65)
Over a decade of experience with preimplantation genetic diagnosis. (2004) (63)
Adverse outcomes of planned and unplanned pregnancies among users of natural family planning: a prospective study. (1997) (62)
Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial (2012) (60)
Evaluating Progestogens for Preventing Preterm birth International Collaborative (EPPPIC): meta-analysis of individual participant data from randomised controlled trials (2021) (58)
Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations. (1975) (58)
Heritable aspects of uterine anomalies. II. Genetic analysis of Müllerian aplasia. (1983) (57)
Gender verification of female athletes (2000) (57)
Pseudovaginal perineoscrotal hypospadias (1972) (56)
Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH) (1997) (56)
Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure. (2009) (56)
Gender verification in the Olympics. (2000) (56)
Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21. (1998) (55)
Birth defects and assisted reproductive technologies. (2014) (54)
Invasive procedures for prenatal diagnosis: any future left? (2012) (53)
Quantity versus quality: Optimal methods for cell-free DNA isolation from plasma of pregnant women (2006) (52)
FALSE-NEGATIVE FINDING ON CHORIONIC VILLUS SAMPLING (1986) (51)
Sex ratio associated with timing of insemination and length of the follicular phase in planned and unplanned pregnancies during use of natural family planning. (1998) (51)
Adverse effects of human leukocyte antigen-DR sharing on fertility: a cohort study in a human isolate. (1985) (51)
What next for preimplantation genetic screening? Randomized clinical trial in assessing PGS: necessary but not sufficient. (2008) (50)
First birth following spindle transfer for mitochondrial replacement therapy: hope and trepidation. (2017) (50)
Abnormalities of human sex chromosomes (1974) (50)
Prenatal diagnosis by use of fetal cells isolated from maternal blood. (1995) (50)
Preimplantation genetic diagnosis (PGD) for heritable neoplasia. (2005) (49)
A solution pathway for preterm birth: accelerating a priority research agenda (2013) (47)
Late First-Trimester Placental Disruption and Subsequent Gestational Hypertension/Preeclampsia (2005) (46)
Gestational diabetes mellitus: a syndrome with phenotypic and genotypic heterogeneity. (1986) (46)
Risk evaluation of CVS (1993) (45)
HLA associations in endometriosis. (1984) (45)
Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. (2014) (45)
Choosing the best prenatal screening protocol. (2005) (44)
Fetal cells in maternal blood: NIFTY clinical trial interim analysis (1999) (44)
ULTRASOUND MARKERS FOR FETAL CHROMOSOMAL DEFECTS (1996) (43)
Gender Verification in Competitive Sports (1993) (42)
Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies. (1983) (42)
Genetic Basis of Endometriosis (2004) (42)
Sol-gel preparation of transparent silica glass (1984) (42)
Risk of neural tube defects in relation to maternal fertility and fertility drug use (1990) (41)
Medical examination for health of all athletes replacing the need for gender verification in international sports. The International Amateur Athletic Federation Plan. (1992) (41)
Timing of conception and the risk of spontaneous abortion among pregnancies occurring during the use of natural family planning. (1995) (40)
Translocations are infrequent among couples having repeated spontaneous abortions but no other abnormal pregnancies. (1989) (40)
Genetics of endometriosis. (2003) (40)
Intact fetal cells in maternal plasma: are they really there? (2003) (39)
Chromosomal microarray versus karyotyping for prenatal diagnosis (2013) (39)
Fetal surgery for myelomeningocele: promise, progress, and problems. (1999) (38)
Cancers of the breast and female genital system: search for recessive genetic factors through analysis of human isolate. (1981) (38)
Gonadal dysgenesis as an autosomal recessive condition. (1969) (38)
Fetus-placenta-newborn☆ (1995) (37)
Gonadal and statural determinants on the X chromosome and their relationship to in vitro studies showing prolonged cell cycles in 45,X; 46,X,del(X)(p11); 46,X,del(X)(q13); and 46,X,del(X)(q22) fibroblasts. (1981) (37)
Spermicides, hormonal contraception and congenital malformations (1990) (37)
Chromosome analysis of ectopic human conceptuses. (1981) (36)
Moral attitudes and beliefs among couples pursuing PGD for sex selection. (2010) (36)
Heritability and Molecular Genetic Studies of Endometriosis (2002) (35)
Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive form. (1996) (34)
Lack of association between antiphospholipid antibodies and first-trimester spontaneous abortion: prospective study of pregnancies detected within 21 days of conception. (1998) (33)
Analysis of LHX8 mutation in premature ovarian failure. (2008) (33)
Children born after preimplantation genetic diagnosis show no increase in congenital anomalies. (2010) (32)
Developing a national collaborative study system for rare genetic diseases (2008) (31)
Parental chromosomal rearrangements associated with repetitive spontaneous abortions. (1981) (30)
Chorionic villus sampling for first-trimester prenatal diagnosis: Northwestern University program. (1985) (30)
Preimplantation diagnosis of genetic and chromosomal disorders (1994) (30)
Chorionic villus sampling in continuing pregnancies. II. Cytogenetic reliability. (1986) (29)
Genetically Determined Sex‐Reversal in 46, XY Humans (1979) (29)
Maternal serum alpha-fetoprotein screening: low and high values for detection of genetic abnormalities. (1986) (29)
Celebrating preimplantation genetic diagnosis of p53 mutations in Li-Fraumeni syndrome. (2001) (29)
Genetics Studies in Incomplete Müllerian Fusion (1984) (28)
Genetic heterogeneity in neural tube defects. (1991) (27)
Novel NR5A1 Missense Mutation in Premature Ovarian Failure: Detection in Han Chinese Indicates Causation in Different Ethnic Groups (2013) (27)
Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF). (2012) (27)
Severity of abnormality influences decision to terminate pregnancies affected with fetal neural tube defects. (1994) (27)
Prenatal effects of maternal-fetal HLA compatibility. (1987) (27)
The reproductive option of sex selection. (1999) (26)
Heritability and candidate genes for endometriosis. (2003) (26)
Good clinical practice advice: Prediction of preterm labor and preterm premature rupture of membranes (2019) (26)
Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. (2015) (26)
Genetic testing of embryos: a critical need for data. (2005) (25)
Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure. (2007) (25)
Preimplantation genetic diagnosis to improve pregnancy outcomes in subfertility. (2012) (25)
Abnormal sexual differentiation in humans. (1982) (25)
FMR1 Premutation Is an Uncommon Explanation for Premature Ovarian Failure in Han Chinese (2014) (24)
Good clinical practice advice: Antenatal corticosteroids for fetal lung maturation (2019) (24)
Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable. (2004) (24)
Developing a core outcome set for future infertility research: an international consensus development study (2020) (24)
Associations between adverse perinatal outcome and serially obtained second- and third-trimester maternal serum alpha-fetoprotein measurements. (1995) (24)
American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism. (1982) (23)
Protein expression profiling of endometriosis: validation of 2-mm tissue microarrays. (2004) (23)
Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status. (2013) (23)
Chronic renal disease, myotonic dystrophy, and gonadoblastoma in XY gonadal dysgenesis (1982) (23)
XY gonadal dysgenesis: Genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis (2004) (23)
Oocyte-specific G-protein-coupled receptor 3 (GPR3): no perturbations found in 82 women with premature ovarian failure (first report). (2008) (23)
Changing indications for preimplantation genetic diagnosis (PGD) (2001) (23)
Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia. (1978) (22)
Familial urinary tract anomalies. (1970) (22)
Unintended pregnancies in women delivering at 18 South American hospitals. NFP-ECLAMC Group. Latin American Collaborative Study of Congenital Malformations. (1998) (22)
First‐trimester biochemical and molecular diagnoses using chorionic villi: High accuracy in the U.S. collaborative study (1992) (22)
Fetal surgery for myelomeningocele? (2002) (21)
Impact of an Academic–Community Partnership in Medical Education on Community Health: Evaluation of a Novel Student-Based Home Visitation Program (2014) (21)
Current status of preimplantation diagnosis (1997) (21)
XX Sex Reversal in the Human (1994) (20)
Chorionic villus sampling in continuing pregnancies. I. Low fetal loss rates in initial 109 cases. (1986) (20)
Good clinical practice advice: Management of twin pregnancy (2019) (20)
Unclassified sex cord-stromal tumors of the ovary: a report of eight cases. (1998) (20)
Infectious processes: an infrequent cause of first trimester spontaneous abortions. (1996) (20)
Hypostatic ulcers in 47,XXY Klinefelter's syndrome (1983) (20)
Chromosomal mosaicism. (1972) (20)
Fetomaternal transfusion depends on amount of chorionic villi aspirated but not on method of chorionic villus sampling. (1990) (19)
Nuclear chromosomal localization in human preimplantation embryos: correlation with aneuploidy and embryo morphology. (2004) (19)
Triploidy (69,XXY) in a liveborn infant. (1972) (19)
Preimplantation genetic diagnosis. (1992) (19)
Isolating fetal cells in the maternal circulation. (1995) (19)
Good clinical practice advice: Iron deficiency anemia in pregnancy (2019) (18)
Abnormalities of the Müllerian and Wolffian duct systems. (1978) (18)
Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction. (2018) (18)
Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differences. (1993) (18)
Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion. (2015) (18)
Growth disadvantage of 45,X and 46,X,del (X) (p11) fibroblasts (1988) (18)
Genetic counseling in translocations. (2002) (17)
Pregnancy and the timing of intercourse. (1995) (17)
Low maternal serum α-fetoprotein and perinatal outcome (1987) (17)
Genetic and Nongenetic Causes of Pregnancy Loss (2009) (17)
Relationship between Y-chromosome length and first-trimester spontaneous abortions. (1983) (17)
Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis (1992) (17)
Carrier screening for cystic fibrosis: implications for obstetric and gynecologic practice. (1991) (17)
Genetic Programming in Ovarian Development and Oogenesis (2007) (17)
Gender testing in the Olympics. (1986) (16)
Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs. (1971) (16)
Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes. (1991) (16)
Cell-free fetal DNA in maternal blood: evolving clinical applications. (2004) (16)
Prenatal genetic testing and treatment for congenital adrenal hyperplasia. (2019) (16)
Comparison of serum placental protein hormone levels in diabetic and normal pregnancy. (1989) (16)
Preimplantation diagnosis and other modern methods for prenatal diagnosis (2017) (16)
Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal). (1989) (16)
Assessing congenital anomalies after preimplantation genetic diagnosis (1996) (15)
Lack of heritability in ovarian germ cell malignancies. (1994) (15)
The Olympic Games and Athletic Sex Assignment. (2016) (15)
Evaluation of a Culture System for Enrichment of CD34+ Hematopoietic Progenitor Cells Present in Maternal Blood (2002) (15)
Detecting fetal DNA from dried maternal blood spots: another step towards broad scale non-invasive prenatal genetic screening and feasible testing. (2003) (15)
Ultrasonic induction of sister chromatid exchanges in human lymphocytes (1981) (14)
Professional self-regulation for preimplantation genetic diagnosis: experience of the American Society for Reproductive Medicine and other professional societies. (2006) (14)
Prenatal diagnosis of congenital muscular dystrophy producing arthrogryposis. (1985) (14)
Transabdominal chorionic villus sampling for first-trimester prenatal diagnosis. (1989) (14)
Role of Preimplantation Genetic Diagnosis (PGD) in Current Infertility Practice (2010) (14)
Genetic screening for cystic fibrosis. (2002) (14)
Good clinical practice advice: First trimester screening and prevention of pre‐eclampsia in singleton pregnancy (2019) (13)
Teratology and Drugs in Pregnancy (2009) (13)
Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam. (1973) (13)
Public objections to designer babies and cloning in USA: not quite what was expected. (2003) (13)
INCREASED MALE-TO-FEMALE SEX RATIO AMONG HLA-DR COMPATIBLE PREGNANCIES (1985) (13)
Endocervical fetal trophoblast for prenatal genetic diagnosis (2006) (13)
Verification of Early Pregnancy Tests in a Multicenter Trial (1987) (12)
Male pseudohermaphroditism: Genetics and Clinical delineation (1978) (12)
Periconceptional use of multivitamins and the prevalence of neural-tube defects. (1990) (12)
Current progress in preimplantation genetic diagnosis (1993) (12)
Relationship between congenital anomalies and contraception (1985) (12)
Vitamins, folic acid and neural tube defects: Comments on investigations in the United States (1991) (12)
Genes and chromosomes that cause female infertility. (1985) (12)
Fetal Cells in Maternal Blood: Prospects for Noninvasive Prenatal Diagnosis. Proceedings of a conference. Arlington, Virginia, September 27-29, 1993. (1994) (12)
Spatial Positioning of All 24 Chromosomes in the Lymphocytes of Six Subjects: Evidence of Reproducible Positioning and Spatial Repositioning following DNA Damage with Hydrogen Peroxide and Ultraviolet B (2015) (12)
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization. (1995) (12)
Bilateral anorchia: discordance in monozygotic twins. (1971) (12)
9 Screening for fetal and genetic abnormalities (1991) (12)
Best Practice & Research Clinical Obstetrics and Gynaecology (2012) (12)
Why are we still talking about chromosomal heteromorphisms? (2017) (11)
Down syndrome is not increased in offspring of natural family planning users (case control analysis) (1995) (11)
Elevated levels of total (maternal and fetal) beta-globin DNA in maternal blood from first trimester pregnancies with trisomy 21. (2007) (11)
Chorionic villus sampling (CVS): World health organization european regional office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis (1992) (11)
Genetic Aspects of Gynecologic Disorders Occurring in 46,XX Individuals (1972) (11)
Vitamins During Pregnancy and Neural Tube Defects (1990) (11)
Risky Business: Meeting the Structural Needs of Transdisciplinary Science. (2017) (11)
Genetic counseling and genetic services in obstetrics and gynecology: implications for educational goals and clinical practice. (1981) (11)
Is cell-free fetal DNA from maternal blood finally ready for prime time? (2012) (11)
Drug ingestion during pregnancy: infrequent exposure in a contemporary United States sample. National Institute of Child Health and Human Development Diabetes in Early Pregnancy Study Group. (1989) (10)
Chromosome territory repositioning induced by PHA-activation of lymphocytes: A 2D and 3D appraisal (2015) (10)
Drugs and Environmental Agents in Pregnancy and Lactation: Embryology, Teratology, Epidemiology (2007) (10)
Hormonal and genetic basis of sexual differentiation disorders and hot topics in endocrinology : proceedings of the 2nd world conference (2013) (10)
Unexplained elevated maternal serum alpha-fetoprotein is not predictive of adverse perinatal outcome in an indigent urban population. (1992) (10)
Disorders of the Gonads, Genital Tract, and Genitalia (2013) (10)
Timing of intercourse. (1995) (10)
Next-generation sequencing for preimplantation genetic diagnosis. (2013) (10)
Genetics of diabetes mellitus (DM) and anomalies in offspring of diabetic mothers. (1978) (10)
Can the Oxytocin Challenge Test Serve as the Primary Method for Managing High‐Risk Pregnancies? (1975) (10)
Failure to detect polycystic kidneys in utero by second trimester ultrasonography (1982) (10)
NAT2 and GSTM1 DNA polymorphisms: increased GSTM1 (active) genotypes in endometriosis (2002) (10)
Phenotypic-Karyotypic Correlations of Gonadal Determinants: Current Status and Relationship to Molecular Studies (1987) (10)
Further evidence that infection is an infrequent cause of first trimester spontaneous abortion. (1996) (10)
Genetic Forms of Gonadal Dysgenesis in 46,XX and 46,XY Individuals (1983) (9)
Xq;autosome translocation in POF: Xq27.2 deletion resulting in haploinsufficiency for SPANX (2011) (9)
Medicine: Blastomeres and stem cells (2006) (9)
Recovery and amplification of placental RNA from dried maternal blood spots: utility for non-invasive prenatal diagnosis. (2006) (9)
Cancer mortality in a human isolate. (1980) (9)
Methodological Problems in Determining Fetal Loss Rates: Relevance to Chorionic Villi Sampling (1985) (9)
Good clinical practice advice: Thyroid and pregnancy (2019) (9)
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women. (2014) (9)
Molecular approach to common causes of female infertility. (2002) (9)
Knowledge of likely time of ovulation and contraceptive use in unintended pregnancies (1999) (9)
The Prenatal Diagnosis of Genetic Disorders (1982) (9)
A general approach to genetic counseling. (2002) (8)
Aetiology of Pregnancy Failure (1992) (8)
Preterm births in countries with a very high human development index – Authors' reply (2013) (8)
Before the beginning: the genetic risk of a couple aiming to conceive. (2019) (8)
Testicular feminisation and inguinal hernia. (1973) (8)
Genetic screening for donors in artificial insemination. (1981) (8)
Interstitial deletion 46,XY,del(1)(q23q25) (1982) (8)
Low fetal loss rates after ultrasound-proved viability in early pregnancy (1988) (8)
Cell-free DNA versus intact fetal cells for prenatal genetic diagnostics: what does the future hold? (2015) (8)
Fetal cells in maternal blood. Overview and historical perspective. (1994) (8)
Toward scientific discussion of human reproductive cloning. (2003) (8)
Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and infertility. (2007) (8)
Genetics of female infertility due to anomalies of the ovary and mullerian ducts. (2014) (8)
Maternal serum alpha-fetoprotein screening in 1987. (1987) (8)
Preimplantation genetic testing to reduce preterm births in assisted reproductive technology (2020) (7)
Prenatal diagnosis and 47,XXY (2013) (7)
Evaluation and Development of a System for Automated Preparation of Blood Specimens for Cytogenetic Analysis (1989) (7)
Low maternal serum alpha-fetoprotein and perinatal outcome. (1987) (7)
Prenatal genetic diagnosis. (1971) (7)
Trisomy 21 and maternal age of menopause: does reproductive age rather than chronological age influence risk of nondisjunction? (2004) (7)
Verification of early pregnancy tests in a multicenter trial. (1987) (7)
Florida International University Herbert Wertheim College of Medicine. (2010) (7)
Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (7)
Metastatic rhabdomyosarcoma presenting as an isolated lateral rectus restriction. (1999) (7)
Necessity of Formal Genetic Screening in Artificial Insemination by Donor (1983) (7)
Association of N-Acetyltransferase 2 (NAT2) genetic polymorphism resulting in decreased capacity to detoxify aromatic amines in women with endometriosis (1998) (7)
Genetic Causes of Premature Ovarian Failure (POF). (2012) (7)
Intrauterine growth retardation in osteogenesis imperfecta. (1978) (6)
ANTENATAL DIAGNOSIS OF CYTOGENETIC ABNORMALITIES (1980) (6)
The Effect of the Elapsed Time Between Blood Draw and Processing on the Recovery of Fetal Cells From Maternal Blood (2004) (6)
Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosis. (1990) (6)
Developing a core outcome set for future infertility research: an international consensus development study. (2020) (6)
Good clinical practice advice: Micronutrients in the periconceptional period and pregnancy (2019) (6)
Pericentric X chromosome ascertained during antenatal diagnosis (1980) (6)
Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance. (1982) (6)
Olympic row over sex testing (1992) (6)
Genetic Causes of Spontaneous Abortion (1993) (6)
The prenatal diagnosis of genetic disorders. (1982) (6)
Quantitative DNA perturbations of p53 in endometriosis: analysis of American and Icelandic cases. (2005) (6)
Hereditary factors in obstetrics and gynecology. (1969) (6)
Screening for down syndrome (2002) (6)
Elevated alpha-fetoprotein and acetylcholinesterase associated with hydrocele. (1984) (6)
Could cloning become permissible (2007) (5)
Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditism. (1971) (5)
Genetics of Spontaneous Abortions (2014) (5)
Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations. (1991) (5)
CHAPTER 5 – Genetic Programming in Ovarian Development and Oogenesis (2000) (5)
Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD (2019) (5)
Genetics of Premature Ovarian Failure: New Developments in Etiology (2017) (5)
Pocket Companion to Accompany Obstetrics: Normal and Problem Pregnancies (2002) (5)
Transvaginal chorionic villus sampling using transabdominal ultrasound guidance: a new technique for first-trimester prenatal diagnosis. (1993) (5)
Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p. (1971) (5)
Pocket Companion to Obstetrics: Normal & Problem Pregnancies (1999) (5)
Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi. (1990) (5)
Antenatal detection of genetic disorders. (1976) (5)
Re: Update on MSAFP Policy Statement from the ASHG. (1990) (5)
Maternal serum screening for fetal down syndrome using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated estriol in adolescents (1993) (5)
Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits (1974) (5)
Developmental anomaly resembling the trisomy 18 syndrome. (1969) (5)
Preterm birth: A clinical enigma and a worldwide public health concern (2020) (5)
Cytogenetic analysis of a case of "13q- syndrome" (46,XX,del 13) using banding techniques. (1980) (5)
Generalized dysmorphia of a similar type in two unrelated babies. (1975) (4)
Isolation and genetic analysis of fetal nucleated red blood cells from maternal blood: the Baylor College of Medicine experience. (1996) (4)
Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband. (1983) (4)
Transvaginal chorionic villus sampling using transabdominal ultrasound guidance (1992) (4)
Smith’s Recognizable Patterns of Human Malformation, 6th ed., Kenneth Lyons Jones (Ed.). Elsevier Saunders, Philadelphia, Pennsylvania (2005), 1, Price: $93.00 (2007) (4)
Novel NR 5 A 1 Missense Mutation in Premature Ovarian Failure : Detection in Han Chinese Indicates Causation in Different Ethnic Groups (2016) (4)
Ovarian Dysgenesis and Premature Ovarian Failure Caused by X Chromosomal Abnormalities (2009) (4)
Where Are the Genes That Cause Endometriosis? (2005) (4)
Prenatal Diagnosis for Pediatricians (1980) (4)
A patient with the Larsen syndrome. (1975) (4)
Do contraceptive methods pose fetal risks? (1985) (4)
Stability of sex chromosome mosaicism. (1980) (4)
Genetic Counseling and Genetic Screening (2007) (4)
Good clinical practice advice: Role of ultrasound in the management of twin pregnancy (2019) (4)
Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS). (2007) (4)
Clinical Implications of Chromosomal Inversions (2008) (4)
Analysis for amniotic fluid crystallization in second-trimester amniocentesis. (1979) (4)
289 Sex and Gender in Sport: Fallacy of the “Level Playing Field” (2010) (4)
Telomere length and aneuploidy: clinical and biological insights into human preimplantation embryos. (2014) (4)
PRENATAL DIAGNOSIS OF CYTOGENETIC DISORDERS (1976) (4)
Closing the folate gap in reproductive-age women (2010) (4)
Diabetes Mellitus: Preventing Anomalies Through Maternal Metabolic Intervention (1986) (4)
Risk of recurrent spontaneous abortion for pregnancies discovered in the fifth week of gestation (1994) (4)
Gender Verification and the Next Olympic Games-Reply (1993) (3)
Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis. (1971) (3)
Genetic Control of Sex Determination (1987) (3)
Novel non-invasive prenatal diagnosis as related to congenital adrenal hyperplasia. (2011) (3)
Yury Verlinsky (01/09/1943–16/07/2009): pioneer in CVS, PGD and hESC (2009) (3)
Gender Testing in the Olympics (1987) (3)
Genetics of Oocyte Depletion (1997) (3)
Fertilisation involving ageing gametes, major birth defects, and Down's syndrome (2002) (3)
Comprar Obstetrics. Normal And Problem Pregnancies (Online And Print) 7th Ed. | Steven G. Gabbe | 9780323321082 | Elsevier Internacional (2016) (3)
Male Pseudohermaphroditism Due to Androgen Insensitivity or 5α-Reductase Deficiency (2009) (3)
XX Gonadal Dysgenesis and Premature Ovarian Failure in 46,XX Individuals (2009) (3)
Chorionic villus sampling: First trimester prenatal diagnosis (1986) (3)
Mutations in mitochondrial histidyl tRNA synthetase (HARS2) is not associated with premature ovarian failure in a cohort of 69 patients (2012) (3)
Contraception and Congenital Malformations (2009) (3)
Repeated suboptimal pregnancy outcome. (1981) (3)
Anencephaly in Three Siblings (1969) (3)
Multifetal Reduction in High-Order Gestations: A Nonelective Procedure? (1996) (3)
Practical Preimplantation Genetic Testing (2020) (3)
Florida International University: Development and Accreditation of Miami’s Public College of Medicine (2009) (3)
FIGO good practice recommendations for reducing preterm birth and improving child outcomes (2021) (3)
Timing of conception and the risk of spontaneous abortion among pregnancies during use of natural family planning. (1994) (2)
Prenatal cytogenetic screening (1995) (2)
Assessing Loss Rates in the Preimplantation Stages of Gestation (1991) (2)
Absence of Close Linkage Between the Locus for Xg and the Locus for Anhidrotic Ectodermal Dysplasia 1 (1969) (2)
Diagnosis and management of the infant with genital ambiguity. (1977) (2)
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation. (1975) (2)
Lower nephron nephrosis in pregnancy. (1952) (2)
The frequency and spectrum of congenital anomalies in natural family planning users in South America: No increase in a case-control study (1997) (2)
Can Pregnancies Be Achieved in Premature Ovarian Insufficiency? (2019) (2)
Gonadal Dysgenesis in 46,XY Females (XY Gender-Reversal) (2009) (2)
Detection of genomic imbalances by comparative genomic hybridization in Chinese fetuses with malformations. (2007) (2)
Screening for fetal and genetic abnormalities. (1991) (2)
Risk factors associated with transcervical CVS losses (1992) (2)
Further comments on amniocentesis in twin gestations. (1983) (2)
Polygenic/Multifactorial Inheritance (2009) (2)
Does unexplained second‐trimester (15 to 20 weeks' gestation) maternal serum α‐fetoprotein elevation presage adverse perinatal outcome? Pitfalls and preliminary studies with late second‐ and third‐trimester maternal serum α‐fetoprotein (1992) (2)
Hypermodal cells, hypomodal cells, and repetitive abortions. (1986) (2)
Clinical Genetics: A Source Book for Physicians (1980) (2)
In vitro fertilization with preimplantation genetic screening. (2007) (2)
Sister chromatid exchanges after exposure to ultrasound and mitomycin C. (1984) (2)
Response from the Editors: First birth following spindle transfer. (2017) (2)
9.2 Advantages and Disadvantages of Competing in International Markets (2020) (2)
Sister chromatid exchange (SCE) frequencies differ between directly prepared cytotrophoblasts and cultured mesenchymal core cells (1991) (2)
Improving assisted reproductive technology pregnancy rates: excluding aneuploid and interrogating euploid embryos. (2015) (2)
Localization of the nucleolar organizer by computer-aided analysis of a variant no. 21 in a human isolate (1979) (2)
Antenatal diagnosis of chromosomal disorders. (1980) (2)
Genetic factors in stillbirths (2011) (2)
Genetic diseases in pregnancy : maternal effects and fetal outcome (1981) (2)
Delayed fertilization and Down's syndrome. (1977) (2)
Prospects for prevention of neural tube defects by vitamin supplementation. (1993) (2)
Genetics of common disorders causing female infertility: part I (2001) (2)
Preface: Genetic screening and counseling. (2010) (2)
Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY. (1974) (2)
Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic villi mosaicism. (1989) (2)
Letter: Bilateral teratoma of testis in 2 brothers with 47,XXY Klinefelter's syndrome. (1976) (2)
I1 Clinical challenges in application of prenatal technologies (2013) (2)
Invasive Prenatal Genetic Techniques (2009) (2)
Antenatal diagnosis of cytogenetic abnormalities. (1981) (2)
Direct analysis of uncultured cytotrophoblastic cells from second- and third-trimester placentas: An accurate and rapid method for detection of fetal chromosome abnormalities (1990) (2)
Commentary re: Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy. (2016) (2)
IMPACT OF EXPANDED CARRIER SCREENING (ECS) ON UPTAKE OF PREIMPLANTATION GENETIC TESTING FOR MONOGENIC DISORDERS (PGT-M) (2019) (2)
Reproductive medicine in a shrinking world. (1996) (1)
GENDER VERIFICATION AND THE NEXT OLYMPIC GAMES. AUTHOR'S REPLIES (1993) (1)
FDA approves 23andMe gene carrier test (2015) (1)
Disorders of gonadal development in humans. (1989) (1)
Down syndrome and natural family planning (1996) (1)
[Late first-trimester invasive prenatal diagnosis--secondary publication. An international randomized trial]. (2005) (1)
Section 4: Fetoscopy and fetal tissue sampling (1981) (1)
Methods of Culture (2014) (1)
Book ReviewMajor Sex-Determining Genes (1980) (1)
Ovarian Dysgenesis and Related Genetic Disorders (1987) (1)
Genetic screening and counseling (2002) (1)
Strategies and Indications for Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) (2020) (1)
Seattle Metropolitan Chapter (SMC) (1999) (1)
Clarification of ECLAMC/NFP case control study (1996) (1)
Preimplantation genetic diagnosis (PGD) for a balanced reciprocal translocation reveals a high proportion (85%) of abnormal embryos. (2001) (1)
GENETICS FOR THE OBSTETRICIAN‐GYNECOLOGIST: QUESTIONS AND ANSWERS (1976) (1)
A prospective study of adverse pregnancy outcomes among planned and unplanned pregnancies in natural family planning users. (1996) (1)
Mammalian Sex Determination (2008) (1)
Noninvasive screening for prenatal genetic diagnosis. (1995) (1)
Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-). (1971) (1)
Caffeine Use During Pregnancy: How Much Is Safe?-Reply (1993) (1)
Comprar Obstetrics: Normal and Problem Pregnancies | Mark Landon | 9780443069307 | Churchill Livingstone (2007) (1)
Noninvasive fetal diagnosis (2012) (1)
Letter: Cytogenetic confirmation of failure of polar-body extrusion. (1973) (1)
Jumping 22q11.21 Translocation: Clinical Consequences and Counseling in an Oligospermic but Otherwise Healthy Adult Male (2005) (1)
PGD : a model to evaluate efficacy? Authors' reply (2006) (1)
Preimplantation Genetic Testing in the Future (2020) (1)
Are we ready for universal genetic screening? (2010) (1)
Increased sister chromatid exchanges in human cell lines characterized by monosomy X or structural abnormalities of the X chromosome (2004) (1)
Preimplantation genetic diagnosis: Its time is now (2016) (1)
Outcome of pregnancy in users of natural family planning. (1989) (1)
Prenatal diagnosis of chromosomal abnormalities using maternal blood. (2002) (1)
Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (1)
More than we ever wanted to know about sex--should we be afraid to ask? (1979) (1)
Fetoscopy, fetal-tissue sampling and the ESHRE guidelines on prenatal diagnosis. (1996) (1)
Genital Duct Anomalies (2009) (1)
FIGO good practice recommendations on the importance of registry data for monitoring rates and health systems performance in prevention and management of preterm birth (2021) (1)
Diabetic control and fetal malformations. (1988) (1)
Cover Story: Noninvasive screening for aneuploidy: who, when, and why? (2000) (1)
GENETIC: GENETIC CAUSES OF PREMATURE OVARIAN FAILURE (POF) AND EARLY MENOPAUSE (2011) (1)
Clinical Outcome of Preimplantation Genetic Testing (2020) (1)
Anatomy of the Pelvis (1996) (1)
Presidents' Page (1999) (1)
Storms of Silence (1996) (1)
Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders (2019) (1)
True Method of Education (2014) (0)
Abstracts From Invited Speakers (2007) (0)
Hypogonadotropic and Hypergonadotropic Hypogonadism in Females: Disorders of Reproductive Ducts (2022) (0)
Cultivation of Taste (2014) (0)
Founder of the Normal School (2014) (0)
Early amniocentesis had similar fetal loss/very preterm delivery rate, compared to late CVS, but more foot defects (2005) (0)
Prevenire il deficit di acido folico nelle donne in età fertile (2011) (0)
7.2 Entrepreneurial Orientation (2020) (0)
8.5 Strategies for Getting Smaller (2020) (0)
David L. Healy, M.D., Ph.D., 1948-2012. (2012) (0)
1.5 Contemporary Critique of Strategic Management (2020) (0)
11.2 Doing Well by Doing Good (2020) (0)
First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) (1990) (0)
Preimplantation genetic diagnosis: Which patients to test and other controversies (2009) (0)
Preimplantation Genetic Testing (PGT) for Human Leukocyte Antigens (HLA) (PGT-HLA) (2020) (0)
Fetal Wastage: Genetic Evaluation (2009) (0)
REPETITIVE SPONTANEOUS ABORTION (1986) (0)
Genetics of male pseudohermaphroditism and true hermaphroditism (1996) (0)
The Journal ofln Vitro Fertilization and Embryo Transfer would like to thank all reviewers for their contri- butions to the Journal by listing their names in alphabetic order. (1986) (0)
HBOC and Lynch syndrome testing: All in a day’s work (2018) (0)
Call for Papers (2004) (0)
3.4 Evaluating the Industry (2020) (0)
9.5 Drivers of Success and Failure When Competing in International Markets (2020) (0)
Single-cell genetic diagnosis: molecular methods and pitfalls (1994) (0)
Major Components of Preimplantation Genetic Testing: Adjustment of Available Genetic Technology to PGT Practice (2020) (0)
3.1 Introduction (2020) (0)
Chapter 3: Evaluating the External Environment (2020) (0)
Chapter 6: Selecting Business-Level Strategies (2020) (0)
P103S Missense Mutation in a Highly Conserved Region of Growth Differentiating Factor - 9 (GDF-9): Single Abnormality Among 62 Women With Premature Ovarian Failure (2005) (0)
Maternal serum alpha-fetoprotein screening: promise not yet fulfilled. (1979) (0)
2.2 Vision, Mission, and Goals (2020) (0)
Chapter 1: Mastering Strategy: Art and Science (2020) (0)
Reviewer Acknowledgment (2013) (0)
8.1 Introduction (2020) (0)
Chapter 33. Klinefelter Syndrome (2010) (0)
8.4 Implementing Corporate Strategy (2020) (0)
9.4 Types of International Strategies (2020) (0)
4.6 Conclusion (2020) (0)
ACOG Clinical Guidelines at a Glance: Prenatal diagnostic testing for genetic disorder (2017) (0)
9.3 CAGE Framework (2020) (0)
11.3 Corporate Governance (2020) (0)
Call for papers (1993) (0)
3.5 Mapping Strategic Groups (2020) (0)
O-45. PGD of a cryptic translocation: implications for segregation products (2002) (0)
The Genetics of Spontaneous Abortions (2020) (0)
The President’s Page (1974) (0)
95018358 Trisomy 21 and maternal age of menopause: Does reproductive age rather than chronological age influence risk of nondisjunction? (1995) (0)
Marker chromosomes in gonadal dysgenesis : avoiding unnecessary surgery (1992) (0)
P-688: Oocyte specific G-protein coupled receptor-3 (GPR3) gene perturbations are not commonly involved in premature ovarian failure (2006) (0)
Nuclear localization of chromosomes in blastomeres from human preimplantation embryos (2003) (0)
Heritable Factors In Gynecologic Cancer (2009) (0)
Vitamin a & birth defects (1998) (0)
4.1 Introduction (2020) (0)
Medical Examination for Health of All Athletes Replacing the Need for Gender Verification in International Sports: The International Amateur Athletic Federation Plan (1992) (0)
Sign Out: Chasing Cassandra (2005) (0)
Medical Genetics: Principles and Practice (1982) (0)
2.5 Conclusion (2020) (0)
Comprar Hormonal and Genetic Basis of Sexual Differentiation Disorders and Hot Topics in Endocrinology: Proceedings of the 2nd World Conference | New, Maria I. | 9781441980014 | Springer (2011) (0)
P-921: Prevention of rhesus alloimmunization: Determination of paternal rhesus D zygosity by plasma DNA analysis prior to preimplantation genetic diagnosis (PGD) (2006) (0)
Incomplete testicular feminization (1974) (0)
1937: Fluorescence In-Situ Hybridization of Sperm Consistent with Gonadal Mosaicism in a Male with Normal Karyotype: Transmission by ICSI Resulting in Recurrent Pregnancy Loss (2007) (0)
Authors' reply (1992) (0)
[Detection of fetal cells in maternal blood: towards a noninvasive prenatal diagnosis]. (1995) (0)
Touch the void with Congress speaker: An introduction to Joe Simpson’s talk at Congress 2010 (2009) (0)
Genética del síndrome de ovarios poliquísticos (2006) (0)
9.7 Conclusion (2020) (0)
Epidermoid carcinoma of the cervix; a statistical study. (1951) (0)
Mass Scale Biosensor Threat Diagnostic for In-Theater Defense Utilization (2012) (0)
Prenatal Diagnosis and Treatment of Genetic Steroid Disorders (2019) (0)
X International Congress of The Society for the Advancement of Contraception Manila, Philippines, 5–9 November 1998 Abstracts (in alphabetical order of author) (1998) (0)
Invasive Diagnostic Procedures for Prenatal Genetic Diagnosis (2000) (0)
Chapter 10: Executing Strategy through Organizational Design (2020) (0)
SOMATIC DNA ALTERATIONS IN ENDOMETRIOSIS: HIGH FREQUENCY OF CHRO-CYP1A1, GSTM1, ENDOMETRIOSIS, SOUTH INDIAN WOMEN MOSOME 17 AND P53 LOSS IN LATE-STAGE ENDOMETRIOSIS (2002) (0)
Occupational and Environmental Perspectives of Birth Defects (2002) (0)
The Educator: THE MEANS OF ELEVATING THE PROFEESSION OF THE EDUCATOR IN PUBLIC ESTIMATION (2014) (0)
Chapter 4: Evaluating the Internal Environment (2020) (0)
True Character of the Educator (2014) (0)
6.2 Understanding Business-Level Strategy through “Generic Strategies” (2020) (0)
10.2 Why Organizational Design (2020) (0)
C39 PGD and ethics: What limits should be assigned to the indications? (2010) (0)
Hahn S., Holzgreve W. Fetal cells and fetal DNA in maternal blood: New developments for a new millennium. Basel: Karger, 2001:1–137. $85.25. (2002) (0)
Genetic source of femininity. (1991) (0)
Transabdominal chorionic villus sampling in a patient with a bicornuate uterus. (1989) (0)
3.6 Conclusion (2020) (0)
The Subfertility Handbook: Early pregnancy loss (2010) (0)
Study Guide for Obstetrics: Normal and Problem Pregnancies (1992) (0)
4.2 Managing Firm Resources (2020) (0)
11.4 Corporate Ethics and Social Responsibility (2020) (0)
1.6 Understanding the Strategic Management Process (2020) (0)
Chapter 11: Leading an Ethical Organization: Corporate Governance, Corporate Ethics, and Social Responsibility (2020) (0)
Novel Therapies for Treating Short Stature withCongenital Adrenal Hyperplasia (2011) (0)
7.7 Conclusion (2020) (0)
6.7 Stuck in the Middle (2020) (0)
Chapter 9: Competing in International Markets (2020) (0)
1.4 The History of Strategic Management (2020) (0)
10.6 Legal Forms of Business (2020) (0)
CV: Joe Leigh Simpson, M.D. (2011) (0)
Maternal serum AFP screening: promise not yet fulfilled. (1979) (0)
2.1 Introduction (2020) (0)
Editorial help (2004) (0)
8.6 Portfolio Planning and Corporate-Level Strategy (2020) (0)
Chapter 2: Assessing Organizational Performance (2020) (0)
The Educator: Connexion of Education with the Character and Position of the Educator (2014) (0)
4.5 Value Chain (2020) (0)
LIST OF Contributors (2022) (0)
CHAPTER 32 – Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders (2003) (0)
Female Sex Anomalies, by Cary M. Dougherty, M.D., and Rowena Spencer, M.D. New York/Evanston/San Francisco/London: Harper & Row, Publishers, 1972, 273 pp., $12.75 (1973) (0)
1.7 Conclusion (2020) (0)
DNA microarrays: A promising new option for prenatal diagnosis (2007) (0)
Noninvasive screening forprenatal genetic diagnosis (1995) (0)
Genetics: Androgen insensitivity (2001) (0)
10.1 Introduction (2020) (0)
5.3 Strategic Issue Identification (2020) (0)
11.5 Contemporary Questions of Corporate Ethics (2020) (0)
The Educator: Prize Essays on the Expediency and Means of Elevating the Profession of the Educator in Society (2008) (0)
6.5 Focused Cost Leadership and Focused Differentation (2020) (0)
DTC genetic testing: What do you tell patients? (2009) (0)
4.3 Resource-Based View (2020) (0)
Place of Preimplantation Genetic Testing (PGT) Among Available Options for Prevention of Genetic Disorders (2020) (0)
10.3 The Basic Building Blocks of Organizational Structure (2020) (0)
The Educator: Education.—Moral Developement as the ground of Knowledge (2014) (0)
4.4 Intellectual Property & Isolating Mechanisms (2020) (0)
Plan of a Normal School (2014) (0)
Genetics In Obstetrics & Gynecology (1992) (0)
Fetal movements and chromosome anomalies (1983) (0)
8.7 Conclusion (2020) (0)
Genetic causes are responsible for most first trimester pregnancy losses (2000) (0)
Selected papers from the 26th Annual Scientific Meeting of the (2008) (0)
Number of Number of Median (range) Number of cells male female cells recovered and identified as cases cases analysed by FISHmale by FISH Centre (2003) (0)
5.2 SWOT Framework (2020) (0)
Sign Out: Prenatal screening isn't perfect (2007) (0)
Criblage du syndrome de down (2007) (0)
6.6 Best-Cost Strategy (2020) (0)
Non-synonymous single nucleotide polymorphism in MCM8 decreased in a cohort of premature ovarian failure patients (2012) (0)
Reply: PGD—a model to evaluate efficacy? (2006) (0)
Reproducing Genetics (2015) (0)
Comprar Obstetrics: Normal and Problem Pregnancies, 6th Edition | Deborah Driscoll | 9781437719352 | Saunders (2012) (0)
Rapid noninvasive detection of fetal RhD in maternal serum of sensitized RhD-negative women by PCR (1998) (0)
The Educator: The Educator a Foster Parent (2014) (0)
Evaluation of chromosome 17 aneuploidy and p53 loss in endometriosis by fluorescence in situ hybridization (FISH). (2001) (0)
Origin of Aneuploidy and Strategies Underlying Clinical Application of Preimplantation Genetic Testing for Chromosomal Disorders (PGT-A and PGT-SR) (2020) (0)
8.2 Corporate-Level Strategy Defined (2020) (0)
Chapter 7: Innovation Strategies (2020) (0)
Hypostatic ulcers in47,XXYKlinefelter's syndrome (1983) (0)
Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (0)
Major Components of Preimplantation Genetic Testing (2020) (0)
Chapter-16 Intact Fetal Cells and Cell-free DNA in Maternal Blood: Definitive Nonivasive Prenatal Diagnosis (2006) (0)
Making sense of the CF screening guidelines (2004) (0)
10.4 Creating an Organizational Structure (2020) (0)
Court sides with Sandoz over Neupogen biosimilar (2015) (0)
LETTERS TO THE EDITORTo the Editor (1979) (0)
7.3 Why Innovate (2020) (0)
Robert G Edwards: visionary for preimplantantion genetic diagnosis (PGD) (2011) (0)
Testicular feminization syndrome. (1969) (0)
Autoradiographic studies of human chromosomes. 3. - The arm ratio of the late-replicating X. (1974) (0)
Editorial and Production Teams (2020) (0)
6.3 Cost Leadership (2020) (0)
Congenital adrenal hyperplasia (2021) (0)
Principles of Human Genetics: Chromosomal and Single‐Gene Disorders (2008) (0)
6.1 Introduction (2020) (0)
ANTENATAL DIAGNOSIS OF GENETIC DISORDERS (1981) (0)
Chapter 13C – Preimplantation Diagnosis and Other Modern Methods for Prenatal Diagnosis (2014) (0)
6.8 Conclusion (2020) (0)
LETTERS TO THE EDITORLetters to the editor (1979) (0)
GENETIC: DO BIRTH DEFECTS INCREASE WITH ASSISTED REPRODUCTIVE TECHNOLOGIES? (2011) (0)
Cytogenetic nomenclature. (1977) (0)
Mutations in Man (1985) (0)
8.3 Diversification (2020) (0)
11.1 Introduction (2020) (0)
The Sound of Gravity (2011) (0)
Letter: Incomplete testicular feminization. (1974) (0)
5.1 Introduction (2020) (0)
Developing a minimum data set, known as a core outcome set, for future infertility research (2020) (0)
3.3 Evaluating the General Environment (2020) (0)
1.2 What is Strategic Management (2020) (0)
10.5 Creating Organizational Control Systems (2020) (0)
P53 perturbations in endometriosis detected by quantitative real-time PCR: further evidence of late somatic DNA alterations (2003) (0)
Molecular profiling of endometriosis using tissue microarrays: Disease correlation with increased expression of estrogen receptor-α (ER-α) and decreased expression of progesterone receptor (PR) (2003) (0)
Nature and Value of Education (2014) (0)
Preface - Vol. 52 (2018) (0)
Highlights of the XVIII FIGO World Congress (XML) (2006) (0)
A quantitative and qualitative examination of couples wishing to pursue IVF with PGD for non-medical sex selection (2009) (0)
The Educator: Expediency of rightly appreciating Education and its Professors (2014) (0)
Abstract presented for the Twenty-third Annual Meeting of the Society of Gynecologic Oncologists March 15–18, 1992Endometrial adenocarcinoma: Genetic analysis indicating heritable site-specific uterine cancer (1992) (0)
Genetics in Medicine (1987) (0)
10.7 Conclusion (2020) (0)
Autoradiographic studies of human chromosomes. 3. Segregation of the no. 13 chromosomes in one family. (1969) (0)
6.4 Differentiation (2020) (0)
Session 10 natural family planning (1995) (0)
Frequency and clinical management of numerical and segmental mosaicism in embryo biopsies obtained for preimplantation genetic testing (PGT) (2020) (0)
7.1 Introduction (2020) (0)
Maternal serum alpha-fetoprotein screening in adolescents (1991) (0)
Reviewer Acknowledgment (2008) (0)
Chapter 8: Selecting Corporate-Level Strategies (2020) (0)
Turner's syndrome (1980) (0)
7.5 Implementing Innovation (2020) (0)
3.2 The Relationship between an Organization and its Environment (2020) (0)
Cytogenetic, Teratogenic, and Miscellaneous Other Disorders Causing Male Pseudohermaphroditism or Germ-Cell Failure in Males (46,XY) and Females (46,XX) (2009) (0)
Chapter 5: Synthesis of Strategic Issues and Analysis (2020) (0)
Preimplantation Genetic Screening and Diagnostic Testing (2015) (0)
Genetic History Taking and Counseling (2009) (0)
9.6 Options for Competing in International Markets (2020) (0)
2.3 Assessing Organizational Performance (2020) (0)
2.4 Competitive Advantage (2020) (0)
Genetic Disorders of Human Sexual Development, by Leonard Pinsky, Robert P. Erickson, and R. Neil Schimke (2001) (0)
The Influence of Maternal Hormones on the Fetus and Newborn Pediatric and Adolescent Endocrinology (2008) (0)
9.1 Introduction (2020) (0)
Implementing Prenatal Carrier Screening for Cystic Fibrosis (2002) (0)
Accessibility (HTML version) (2020) (0)
Antenatal monitoring of genetic disorders. (1979) (0)
Erroneous and unjust Conduct of Individuals and the Public concerning Education and its Professors (2014) (0)
7.4 Types of Innovation (2020) (0)
ART and offspring anomalies: How concerned should we be? (2005) (0)
1.3 Intended, Emergent, and Realized Strategies (2020) (0)
Verlinsky Y, Kuliev A. An Atlas of Preimplantation Genetic Diagnosis. New York: The Parthenon Publishing Group, 2000:1–174. (2001) (0)
How frequent are chromosomal abnormalities in spontaneous abortuses? reassessment on the basis of chorionic villus vs. embryonic cultures (1985) (0)
Safety of frozen semen. (1979) (0)
R--short-limbed dwarfism. (1974) (0)
7.6 Responding to Innovation in the Market (2020) (0)
Expanding Indications for Preimplantation Genetic Testing (PGT) – Impact on ART Practices (2020) (0)

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What Schools Are Affiliated With Joe Leigh Simpson?

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