Ernest B. Hook

Ernest B. Hook's AcademicInfluence.com Rankings

Ernest B. Hook

Medical

#1861

World Rank

#2240

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Epidemiology

#293

World Rank

#310

Historical Rank

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Ernest B. Hook'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

Capture-recapture methods in epidemiology: methods and limitations. (1995) (748)
Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use. (1977) (491)
Rates of Chromosome Abnormalities at Different Maternal Ages (1981) (427)
Chromosomal abnormality rates at amniocentesis and in live-born infants. (1983) (351)
The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism (2004) (271)
Dietary cravings and aversions during pregnancy. (1978) (193)
Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories. (1989) (190)
The value of capture-recapture methods even for apparent exhaustive surveys. The need for adjustment for source of ascertainment intersection in attempted complete prevalence studies. (1992) (187)
Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical Cytogeneticists. (1996) (171)
Cardiovascular birth defects and antenatal exposure to female sex hormones. (1977) (165)
Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss (2014) (161)
Nausea and vomiting of pregnancy and association with pregnancy outcome. (1986) (147)
The natural history of cytogenetically abnormal fetuses detected at midtrimester amniocentesis which are not terminated electively: new data and estimates of the excess and relative risk of late fetal death associated with 47,+21 and some other abnormal karyotypes. (1989) (139)
Down syndrome in live births by single year maternal age interval in a Swedish study: comparison with results from a New York State study. (1978) (131)
The Association Between Maternal Serum Alpha‐Fetoprotein and Preterm Birth, Small for Gestational Age Infants, Preeclampsia, and Placental Complications (1996) (118)
Chromosome abnormalities and spontaneous fetal death following amniocentesis: further data and associations with maternal age. (1983) (112)
Rates of Down syndrome at livebirth by one-year maternal age intervals in studies with apparent close to complete ascertainment in populations of European origin: a proposed revised rate schedule for use in genetic and prenatal screening. (1996) (109)
Validity of methods for model selection, weighting for model uncertainty, and small sample adjustment in capture-recapture estimation. (1997) (101)
Goodness-of-fit based confidence intervals for estimates of the size of a closed population. (1984) (101)
The impact of aneuploidy upon public health: mortality and morbidity associated with human chromosome abnormalities. (1985) (94)
Effect of variation in probability of ascertainment by sources ("variable catchability") upon "capture-recapture" estimates of prevalence. (1993) (93)
International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age (1999) (93)
The imprecision in rates of down syndrome by 1‐year maternal age intervals: A critical analysis of rates used in biochemical screening (1994) (87)
The consequences of chromosome imbalance: Principles, mechanisms, and models (1987) (83)
Maternal age-specific rates of 47,+21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: comparison with rates expected from observations at amniocentesis. (1988) (82)
Cerebral gigantism: endocrinological and clinical observations of six patients including a congenital giant, concordant monozygotic twins, and a child who acheived adult gigantic size. (1967) (81)
The effects of model selection on confidence intervals for the size of a closed population. (1991) (81)
Joint estimation of Down syndrome risk and ascertainment rates: a meta‐analysis of nine published data sets (1998) (80)
Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age. (1987) (79)
The natural history of Down syndrome conceptuses diagnosed prenatally that are not electively terminated. (1995) (75)
Use of Bernoulli census and log-linear methods for estimating the prevalence of spina bifida in livebirths and the completeness of vital record reports in New York State. (1980) (74)
Accuracy of alternative approaches to capture-recapture estimates of disease frequency: internal validity analysis of data from five sources. (2000) (73)
Spontaneous deaths of fetuses with chromosomal abnormalities diagnosed prenatally (1978) (68)
Inherited ring chromosomes: an analysis of published cases (1991) (67)
Second-trimester maternal serum alpha-fetoprotein levels and the risk of subsequent fetal death. (1991) (65)
DEOXYRIBONUCLEIC-ACID REPLICATION PATTERN OF TRISOMY D1. (1964) (65)
Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, parental-age associations, sex-ratio trends, and comparisons with rates of mutants. (1984) (60)
Recommendations for presentation and evaluation of capture-recapture estimates in epidemiology. (1999) (57)
Prematurity in Scientific Discovery: On Resistance and Neglect (2002) (56)
Influence of cravings and aversions on diet in pregnancy (1985) (56)
Outcasts from evolution: Scientific attitudes of racial inferiority, 1859–1900 (1972) (56)
Cigarette smoking and Down syndrome. (1985) (53)
Incidence and prevalence as measures of the frequency of birth defects. (1982) (51)
International Commission for Protection against Environmental Mutagens and Carcinogens. (1983) (51)
Deoxyribonucleic acid replication and mapping of the D-1 chromosome. A study of two patients with partial trisomy D-1. (1966) (46)
Maternal cigarette smoking, Down syndrome in live births, and infant race. (1988) (46)
Rates of mutant structural chromosome rearrangements in human fetuses: data from prenatal cytogenetic studies and associations with maternal age and parental mutagen exposure. (1983) (46)
IDENTIFICATION OF THE MONGOLISM CHROMOSOME BY DNA REPLICATION ANALYSIS. (1965) (46)
Validity of Bernoulli census, log-linear, and truncated binomial models for correcting for underestimates in prevalence studies. (1982) (45)
Frequency of Down syndrome in livebirths by single-year maternal age interval: results of a Massachusetts study. (1978) (45)
Maternal alcohol and tobacco consumption and their association with nausea and vomiting during pregnancy (1979) (41)
Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20 000 prenatal studies compared with estimated rates in live births (2004) (41)
Estimated rates of Down syndrome in live births by one year maternal age intervals for mothers aged 20-49 in a New York State study-implications of the risk figures for genetic counseling and cost-benefit analysis of prenatal diagnosis programs. (1977) (40)
A search for a paternal-age effect upon cases of 47, +21 in which the extra chromosome is of paternal origin. (1984) (40)
FAMILIAL D~D TRANSLOCATION. REPORT OF A PEDIGREE AND DNA REPLICATION ANALYSIS. (1964) (38)
Use of capture-recapture analyses in fetal alcohol syndrome surveillance in Alaska. (1995) (38)
Congenital asymmetry associated with trisomy 18 mosaicism. (1965) (37)
Down's syndrome: percentage reporting on birth certificates and single year maternal age risk rates for Ohio 1970-79: comparison with upstate New York data. (1981) (37)
Internal validity analysis: a method for adjusting capture-recapture estimates of prevalence. (1995) (36)
Maternal age, paternal age, and human chromosome abnormality: nature, magnitude, etiology, and mechanisms of effects. (1985) (32)
How much difference does chromosome banding make?: Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities (1989) (32)
Spontaneous deaths of fetuses with chromosomal abnormalities diagnosed prenatally. (1979) (31)
Alpha-fetoprotein: a biomarker for pregnancy outcome. (1993) (31)
A simple function for maternal-age-specific rates of Down syndrome in the 20-to-49-year age range and its biological implications. (1980) (30)
Sister chromatid exchanges in ataxia telangiectasia. (1976) (30)
Contribution of chromosome abnormalities to human morbidity and mortality. (1982) (28)
Paternal age and Down's syndrome genotypes diagnosed prenatally: No association in New York State data (2004) (28)
Search for ethnic, geographic, and other factors in the epidemiology of Down syndrome in South America: analysis of data from the ECLAMC project, 1967-1997. (2001) (28)
Differences in maternal age-specific rates of Down syndrome between Jews of European origin and of North African or Asian origin. (1979) (27)
A search for evidence for a paternal age effect independent of a maternal age effect in birth certificate reports of Down's syndrome in New York state. (1980) (27)
Elevated maternal age‐specific rates of Down syndrome liveborn offspring of women of Mexican and Central American origin in California (1999) (26)
Distribution of sex chromosome complements in 651 patients with turners syndrome (1980) (26)
Perspectives in mutation epidemiology: 3. Contribution of chromosome abnormalities to human morbidity and mortality and some comments upon surveillance of chromosome mutation rates (1983) (26)
Perspective in mutation epidemiology. 2. Epidemiologic and design aspects of studies of somatic chromosome breakage and sister-chromatid exchange. (1982) (26)
Female predominance (low sex ratio) in 47,+21 mosaics. (1999) (25)
Trends in utilization of prenatal cytogenetic diagnosis by New York State residents in 1979 and 1980. (1983) (25)
Early in vitro division of PHA stimulated cord blood lymphocytes: implications for study of chromosome breakage. (1976) (24)
Conceptus viability, malformation, and suspect mutagens or teratogens in humans. The Yule-Simpson paradox and implications for inferences of causality in studies of mutagenicity or teratogenicity limited to human livebirths. (1991) (24)
Temporal increase in the rate of Down syndrome livebirths to older mothers in New York State. (1981) (24)
Human teratogenic and mutagenic markers in monitoring about point sources of pollution. (1981) (24)
Paternal age. (1983) (24)
Some aspects of the epidemiology of human minor birth defects and morphological variants in a completely ascertained newborn population (Madison study). (1976) (23)
Alpha‐Fetoprotein: A Biomarker for Pregnancy Outcome (1993) (22)
What kind of controls to use in case control studies of malformed infants: recall bias versus "teratogen nonspecificity" bias. (2000) (22)
Use of Prenatal Cytogenetic Diagnosis in New York State (1981) (22)
The frequency of 47,+21, 47,+18, and 47,+13 at the uppermost extremes of maternal ages: results on 56,094 fetuses studied prenatally and comparisons with data on livebirths (2004) (22)
Chromosome abnormalities in older women by maternal age: evaluation of regression-derived rates in chorionic villus biopsy specimens. (1990) (21)
Spontaneous abortion and subsequent Down syndrome livebirth (2004) (21)
Down syndrome rates and relaxed selection at older maternal ages. (1983) (21)
Cardiovascular birth defects and prenatal exposure to female sex hormones: a reevaluation of data reanalysis from a large prospective study. (1992) (20)
Parental age and unbalanced Robertsonian translocations associated with Down syndrome and Patau syndrome: comparison with maternal and paternal age effects for 47, + 21 and 47, + 13 (1984) (20)
Folic acid: abortifacient or pseudoabortifacient? (2000) (19)
Evidence for Selective Differences between Cells with an Active Horse X Chromosome and Cells with an Active Donkey X Chromosome in the Female Mule (1971) (19)
Issues in analysis of data on paternal age and 47,+21: implications for genetic counseling for Down syndrome (1987) (19)
Variability in predicted rates of Down syndrome associated with elevated maternal serum alpha-fetoprotein levels in older women. (1988) (18)
Decreased HLA heterogeneity in parents of children with Down syndrome. (1983) (18)
Evaluation of a temporal increase in ventricular septal defects: estimated prevalence and severity in northeastern New York, 1970-1983. (1988) (17)
PATERNAL AGE AND EFFECTS ON CHROMOSOMAL AND SPECIFIC LOCUS MUTATIONS AND ON OTHER GENETIC OUTCOMES IN OFFSPRING (1986) (17)
Rates of 47, + 13 amd 46 translocation D/13 Patau syndrome in live births and comparison with rates in fetal deaths and at amniocentesis. (1980) (17)
False‐positive reporting of Down syndrome on Ohio and New York birth certificates (1985) (17)
An analysis of paternal age and 47,+21 in 35,000 new prenatal cytogenetic diagnosis data from the New York State Chromosome Registry: no significant effect (1987) (17)
"Incidence" and "prevalence" as measures of the frequency of congenital malformations and genetic outcomes: application to oral clefts. (1988) (17)
Paternal age and Down syndrome in British Columbia. (1995) (14)
Comparison of mathematical models for the maternal age dependence of Down's syndrome rates (2004) (14)
A Trichomonas species in a mixed microbial meningitis. (1976) (14)
Influence of pregnancy on dietary selection. (1980) (14)
Death certificate reports of cardiovascular disorders in children: comparison with diagnoses in a pediatric cardiology registry. (1977) (13)
On the need for a 16th and 17th recommendations for capture-recapture analysis. (2000) (13)
Issues pertaining to the impact and etiology of trisomy 21 and other aneuploidy in humans; a consideration of evolutionary implications, maternal age mechanisms, and other matters. (1989) (13)
Interrelationships of Relative Risks of Birth Defects in Embryonic and Fetal Deaths, in Livebirths, and in All Conceptuses (1992) (13)
Normal or affected controls in case-control studies of congenital malformations and other birth defects: reporting bias issues. (1993) (13)
Capture-recapture estimation. (1995) (13)
INTERPRETATION OF RECENT DATA PERTINENT TO GENETIC COUNSELING FOR DOWN SYNDROME: MATERNAL-AGE-SPECIFIC-RATES, TEMPORAL TRENDS, ADJUSTMENTS FOR PATERNAL AGE, RECURRENCE RISKS, RISKS AFTER OTHER CYTOGENETIC ABNORMALITIES, RECURRENCE RISK AFTER REMARRIAGE (1982) (13)
D.N.A. REPLICATION ANALYSIS IN IDENTIFYING THE CYTOGENETIC DEFECT IN DOWN'S SYNDROME (MONGOLISM). (1965) (12)
The ratio of de novo unbalanced translocation to 47, trisomy 21 Down syndrome. A new method for human mutation surveillance and an apparent recent change in mutation rate resulting in human interchange trisomies in one jurisdiction. (1978) (12)
Maternal age-specific rates of chromosome abnormalities at chorionic villus study: a revision. (1989) (11)
Rates of trisomy 18 in livebirths, stillbirths, and at amniocentesis. (1979) (11)
Maternal age‐specific rates of Down syndrome used in serum screening are biased low (2000) (11)
Mutation rates for unbalanced Robertsonian translocations associated with Down syndrome. Evidence for a temporal change in New York State live births 1968--1977. (1981) (10)
Representative and misrepresentative associations of birth defects in livebirths. Conditions under which relative risks greater than unity in livebirths necessarily imply relative risks greater than unity in all conceptuses. (1993) (10)
Marginal versus conditional versus 'structural source' models: a rationale for an alternative to log-linear methods for capture-recapture estimates. (1998) (10)
HERELLEA MENINGITIS FOLLOWING VENTRICULOGRAPHY. (1964) (10)
Re: "Neighborhood social environment and risk of death: multilevel evidence from the Alameda County study". (2000) (9)
Accuracy of Capture-Recapture Estimates of Prevalence (2012) (9)
DEOXYRIBOSE-NUCLEIC-ACID REPLICATION PATTERN OF TRISOMY 18. (1964) (9)
Unbalanced Robertsonian translocations associated with Down's syndrome or Patau's syndrome: Chromosome subtype, proportion inherited, mutation rates, and sex ratio (2004) (9)
Racial differentials in the prevalence rates of males with sex chromosome abnormalities (XXY, XYY) in security settings in the United States. (1974) (9)
Factual, statistical and logical issues in the search for a paternal age effect for Down syndrome (1990) (8)
Apparent sex difference in spontaneous closure of ventricular septal defect. (1978) (8)
Sister-chromatid exchange and phototherapy. (1979) (8)
Muddling genetic discrimination. (1992) (8)
Genetic distinctions are not necessarily examples of genetic discrimination. (1992) (8)
Statistical and logical considerations in evaluating the association of prenatal folic-acid supplementation with pregnancy loss. (2001) (8)
NAUSEA AND VOMITING OF PREGNANCY — A FETO-PROTECTIVE MECHANISM AGAINST EMBRYOTOXINS? (1974) (8)
Genetic counseling dilemmas: Down syndrome, paternal age, and recurrence risk after remarriage. (1980) (7)
Paternal age and Down syndrome in British Columbia. (1981) (7)
Completeness of Reporting: Capture–Recapture Methods in Public Health Surveillance (2003) (7)
Rates of Down's syndrome at the upper extreme of maternal age--absence of a "leveling" effect and evidence for artifacts resulting from analyses of rates by five-year maternal age intervals. (1980) (7)
TRISOMY-18 SYNDROME IN A PATIENT WITH NORMAL KARYOTYPE, CLINICAL AND DERMATOGLYPHIC FINDINGS. (1965) (7)
Why is the XX Fitter? Evidence Consistent with an Effect of X-heterosis in the Human Female from Sex Ratio Data in Offspring of First Cousin Marriages (1973) (6)
Comparison of quantitative autoradiographic DNA replication patterns of human chromosomes obtained using 3H-deoxycytidine and 3H-thymidine as precursors. (1973) (6)
Somatic chromosome breakage in low birth weight newborns. (1981) (6)
Glucose-6-phosphate dehydrogenase Madrona: a slow electrophoretic glucose-6-phosphate dehydrogenase variant with kinetic characteristics similar to those of normal type. (1968) (6)
Congenital malformations worldwide: A report from the international clearinghouse for birth defect monitoring systems (1992) (6)
Current difficulties in use of maternal serum alpha-fetoprotein levels in counseling mid-trimester older pregnant women regarding risk of a Down syndrome fetus. (1988) (5)
Sister-chromatid exchanges in newborns: apparent drop immediately after birth. Does this reflect two different populations of lymphocytes? (1986) (5)
Timely monthly surveillance of birth prevalence rates of congenital malformations and genetic disorders ascertained by registries or other systematic data bases. (1990) (5)
2. Prematurity in Scientific Discovery (2017) (5)
Analyses of data on rates of cytogenetic disorders in live births. (1978) (5)
Problems in interpretation of reported birth prevalence rates of neural tube defects. (1983) (5)
Negative outcome of a blind assessment of the association between spray adhesive exposure and human chromosome breakage (1974) (5)
An investigation of dermatoglyphic asymmetry in rubella embryopathy. (1971) (5)
Invited editorial: Genetic triage and genetic counseling (1984) (5)
On the inadequacy of quinquennial data for analyzing the paternal age effect on Down's dyndrome rates (2004) (5)
Cytogenetics, environment, and malformation syndromes (1977) (5)
PATERNAL AGE AND GENETIC OUTCOME: IMPLICATIONS FOR GENETIC COUNSELING (1986) (4)
An Exact Test for All‐Way Interaction in A 2 M Contingency Table: Application to Interval Capture–Recapture Estimation of Population Size (1999) (4)
Gestational age at maternal serum alpha-fetoprotein screening and the detection of Down syndrome. (1990) (4)
Single Hit Aetiology of Human Minor Congenital Malformations unassociated with Major Congenital Malformations (1970) (4)
Appendix: A general regression model for analysis of independent maternal and paternal age effects for 47,+21 and other disorders that may arise from mutant gametes from either parent (1987) (4)
A pilot screening study of chromosome breakage in cultured blood cells from newborn infants. (1972) (4)
Surveillance of Germinal Human Mutations for Effects of Putative Environmental Mutagens and Utilization of a Chromosome Registry in Following Rates of Cytogenetic Disorders (1987) (4)
Maternal exposure to oral contraceptives and other female sex hormones: relation to birth defects in a prospectively ascertained cohort of 50282 pregnancies. (Abstract only) (1974) (4)
The human simian crease and its variants. A model for investigation of serious congenital malformation. (1974) (4)
Estimates of the likelihood that a Down's syndrome child of unknown genotype is a consequence of an inherited translocation. (1980) (3)
Unequal adaptive value of changing cigarette use during pregnancy for heavy, moderate, and light smokers (1994) (3)
The distalmost palmar axial triradius in children with selected types of isolated congenital heart disease. (1974) (3)
Differences between rates of trisomy 21 (Down syndrome) and other chromosomal abnormalities diagnosed in livebirths and in cells cultured after second-trimester amniocentesis--suggested explanations and implications for genetic counseling and program planning. (1978) (3)
Aneuploidy. Bond DJ, Chandley AC, (Oxford Monographs on Medical Genetics No. 11). Oxford and New York: Oxford University Press, 1983 (1985) (3)
Abortions because of unavailability of prenatal diagnosis. (1981) (3)
Parathenar palmar pattern: a dermatoglyphic sign of possible clinical significance. (1975) (3)
Risk of Down syndrome among relatives of Down syndrome individuals. (1985) (3)
Geneticophobia and the Implications of Screening for the XYY Genotype in Newborn Infants (1976) (3)
Use of computer simulation to evaluate a putative cluster of genetic or teratologic outcomes: Adjustment for “multiple hypotheses” and application to a reported excess of Down's syndrome (1997) (3)
Human germinal mutations: monitoring for environmental effects. (1979) (3)
Central Nervous System Infection in Hydrocephalic Children Following Ventriculography (1965) (3)
The XYY Syndrome and Klinefelter's Syndrome. (1974) (3)
Dorothy Warburton (1936-2016). (2016) (3)
Cardiovascular birth defects and prenatal exposure to female sex hormones: a reevaluation of data reanalysis from a large prospective study. (1992) (2)
Does fetal growth retardation explain the association between Down syndrome and low levels of maternal serum alpha‐fetoprotein? (1992) (2)
Re: "Use of Bernoulli census and log-linear methods for estimating the prevalence of spina bifida in livebirths and the completeness of vital record reports in New York State". (1993) (2)
Gender Bias and Ida Noddack (2003) (2)
Epidemiology and Population Monitoring in Genetic Risk Assessment (1984) (2)
Why is the XX Fitter? Evidence Consistent with an Effect of X-heterosis in Women from Sex Ratio Data in Offspring of First Cousin Marriages (1973) (2)
ENVIRONMENTAL FACTORS AND HUMAN BIRTH DEFECTS: INTERPRETATION OF RELATIVE RISKS IN CLINICAL GENETICS (1986) (2)
Age of ascertainment: an index of relative severity of cytogenetic conditions. (1982) (2)
Genetic triage and genetic counseling. (1984) (2)
Human genetics: Problems and approaches. F. Vogel and A. G. Motulsky, Berlin and New York: Springer-Verlag, 1979, 700 pages + xxviii, $49.50 (1981) (2)
Prenatal screening for neural tube defects and chromosome abnormalities: the complexities of program evaluation. (1995) (2)
Rates of Down syndrome at the upper extreme of maternal age: considerations and recommendations in analysis (2006) (2)
Acquired traits: Memoirs of a geneticist from the Soviet Union (1991) (2)
“Human behavior and genetics.” Schmid W. Nielsen J (ed), Amsterdam: Elsevier‐North Holland, 1981. 253 pp. (1982) (1)
Screening for Down syndrome: Reply to Wald et al. (1989) (1)
Does ascertainment bias contribute to the reported association of omphalocele and gastroschisis with other birth defects in families but not in individuals? (1993) (1)
Chromosome breakage in low birth weight newborns. (1976) (1)
James Watt Mavor (1883-1963): A Forgotten Discoverer of Radiation Effects on Heredity (2015) (1)
Letters to the Editors (2004) (1)
Consanguinity and Down syndrome in the Shetland Islands (1992) (1)
ESTIMATED RATES OF DOWN'S SYNDROME IN LIVEBIRTHS BY SINGLE YEAR MATERNAL AGE INTERVAL BETWEEN 20–49 AND IMPLICATIONS FOR COST-BENEFIT ANALYSIS OF PRENATAL DIAGNOSIS PROGRAMS (1977) (1)
Choroid plexus cysts diagnosed prenatally as an independent risk factor for cytogenetic abnormality (1993) (1)
A guide to the genetics collections of the American philosophical society (1990) (1)
Polygenes versus one gene plus chance: what are the real differences? (1988) (1)
An artifact in evaluation of paternal age trends for Down syndrome. (1984) (1)
Possible unanticipated protective effects of agents: An additional reason for using both normal and malformed controls in case‐control studies of birth defects (2000) (1)
Estimation and the nature of controls in birth defect studies. (1993) (1)
Reply to Mitchell et al. (1994) (1)
Interpretation of reported live birth maternal age–specific rates on an ostensibly white population in data from the National ‘Down syndrome’ Register (2004) (1)
Models and assumptions in calculating the probabilities of detecting chromosomal mosaicism (1978) (1)
ICPEMC working paper 5/3. Perspectives in mutation epidemiology. III: Contribution of chromosome abnormalities to human morbidity and mortality and some comments upon surveillance of chromosome mutation rates (1984) (1)
Shakespeare, genetics, malformations, and the Wars of the Roses: hereditary themes in Henry VI and Richard III. (1987) (1)
Sister chromatid exchange in newborns (2004) (1)
Capture-recapture estimates of cancer incidence, adjusting for geographic effects: an alternative perspective. (1996) (1)
Massachusetts Department of Public Health. Use of prenatal cytogenetic diagnosis in New York State. (1981) (1)
Response to Teratology Society statement about the risks of excessive doses of vitamin A. (1987) (1)
Consequences of a nationwide ban on spray adhesives alleged to be human teratogens and mutagens (1976) (1)
Problem of offering unsolicited clinical genetic advice and diagnoses to nonmedical friends and strangers. (1997) (1)
A method for the detection of the contribution of X heterosis to female survival by comparison of sex ratios of offspring from consanguineous matings. (1969) (1)
On the Republication of Sidney Hook's Towards the Understanding of Karl Marx (2015) (0)
25. Extensions and Complexities: In Defense of Prematurity in Scientific Discovery (2019) (0)
Comment on comparison of settings for study of the prevalence of XYY genotype (1975) (0)
Etiology and pathogenesis of down syndrome, C.J. Epstein, T. Hassold, I.T. Lott, L. Nadel, and D. Patterson, eds. New York: Wiley‐Liss, 1995, 260 pages, $110.00 (1996) (0)
Relation of the crude relative risk of a disorder to relative risks in strata of a "susceptible" variable. (1993) (0)
Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss (2014) (0)
Female sex hormone exposure and human congenital defects. (Abstract only) (1974) (0)
Hereditary Themes in Shakespeare's Poetry (2015) (0)
Advances in teratology. Vol. 4. By D. H. M. Woollam, ed. Academic Press, New York. 240 pp. 1970 (1971) (0)
Temporal aspects of changes in neural tube defect rates. (2003) (0)
Genetic-counseling implications for cleft lip if an autosomal recessive major locus accounts for all cases. (1993) (0)
Interpreting the legacy of Sidney Hook (1997) (0)
Spray adhesives and alleged genetic teratologic hazards: policy implications (1975) (0)
The genetics of altruism. Boorman, Scott A. and Levitt, Paul R. New York: Academic Press, 1980, $29.50 (1983) (0)
Epidemiology of congenital malformations (1993) (0)
Chromosome mutation and neoplasia. James German (ed). New York: Alan R. Liss, Inc., 1983 (1985) (0)
Apparent “in situ” clone of cytogenetically marked ataxia-telangiectasia lymphocytes (1975) (0)
SOME COMMENTS ON THE SIGNIFICANCE OF SEX CHROMOSOME ABNORMALITIES IN HUMAN MALES (1972) (0)
Corrigendum (1993) (0)
Selected topics in medical genetics. C. A. Clarke, ed. Oxford University Press, London, 282 pp. 1969. Price unstated (1969) (0)
Roundtable Discussion: Human Aspects of Aneuploidy (1985) (0)
William Egginton, The Man Who Invented Fiction: How Cervantes Ushered in the Modern World. Bloomsbury, 2016. (2017) (0)
Temporal increase intherateofDownsyndrome livebirths toolder mothers inNewYorkState (1981) (0)
On the conspiracy theory of injury epidemiology. (1994) (0)
Book Review:Aneuploidy. Part A: Incidence and Etiology. Baldev K. Vig, Avery A. Sandberg (1988) (0)
Essentials of Biostatistics. (1994) (0)
10. Interdisciplinary Dissonance and Prematurity: Ida Noddack’s Suggestion of Nuclear Fission (2019) (0)
Educational resources: Report review: Teaching genetics to medical students: A survey and recommendations. Report of a working party of the committee on clinical genetics of the royal college of physicians. (1991) (0)
Dietary cravings and aversions during pregnancy and association with pregnancy outcome (1989) (0)
Letter: Brain research, violent behavior, and the XYY genotype: Comments on the NINDS report. (1976) (0)
James Van Gundia Neel, papers, ca. 1935-1999 (2014) (0)
1612 FRACTIONAL EXCRETION OF SODIUM IN LOW BIRTH WEIGHT INFANTS (1985) (0)
Some issues in the study of birth defects and recurrence risks in live births and "stillbirths". (1990) (0)
Letters To The Editor (1933) (0)
Andrew Robinson. Earth-Shattering Events: Earthquakes, Nations, and Civilizations . London and New York: Thames & Hudson, 2016 (2019) (0)
Letter: Question regarding pooled data. (1975) (0)
Estimates ofthelikelihood that aDown'ssyndrome child ofunknown genotype isa consequenceofan inherited translocation (1980) (0)
Estimating racial and geographical variation in Down syndrome incidence (1999) (0)
Reply to Wiseman (1994) (0)
Reply to Wiseman and Dodds‐Smith (1994) (0)
Methodology Questioned (1976) (0)
The efficacy of sterile gauze as a filter for air ventriculography and pneumoencephalography (1965) (0)
Medical genetics. Proceedings of the symposium at Debrecen-Hajdus-Zoboszlo (1980) (0)
Asymmetric manifestations of an apparently new syndrome: depressed and pitted skin, facial tumors, syndactyly, and other congenital defects. (1968) (0)
Simpler common-sense methods may be preferable to "empirical Bayes". (1995) (0)
Subject Index, Vol. 25, 1975 (1975) (0)
CHROMOSOMAL BREAKAGE AND SPRAY ADHESIVE EXPOSURE (1974) (0)
Minor malformations in the neonate. K. Mehes, Budapest: Akademiai Kiado (Publishing house of the Hungarian Academy of Sciences), 1983, 129 pp (1984) (0)
Question Regarding Pooled Data (1975) (0)
528 AN APPARENT CHANGE IN MUTATION RATE5 FOR INTERCHANGE TRISOMY 21 IN LIVEBIRTHS (1978) (0)
Aneuploidy (2019) (0)
Observations on the rate of chromosome breakage in cells cultured from umbilical cord blood in relation to infant birth weight. (1973) (0)
1. A Background to Prematurity and Resistance to “Discovery” (2019) (0)
Anencephaly, other congenital malformations, and stillbirths. (1986) (0)
Basic Biostatistics for Geneticists and Epidemiologists: A Practical Approach (2010) (0)
Genetic Decision Making and Pastoral Care (1983) (0)
Letters to the editors (2004) (0)
The Exclusion of Minor Malformations in the Study of Mutation in the Offspring of Survivors of Atomic Bombs: Methodological, Not Sociopolitical, Rationale (1997) (0)
Suffering made Real: American Science and the Survivors at Hiroshima. By M. SUSAN LINDEE. (1996) (0)
Response to christanson and torfs. (1988) (0)
Neural tube defects and viability: what is a "stillbirth" in Newfoundland? (1987) (0)
Down syndrome live births and prior spontaneous abortions of unknown karyotype. (1985) (0)
Letter: Methodology questioned. (1976) (0)
Human congenital malformations. The design of a computer‐aided study. E. Gal and I. Gal. Butterworths, Boston, 1975, X + 194 pp (1976) (0)

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