Neil J. Risch

Q: What Schools Are Affiliated With Neil J. Risch

Neil J. Risch is affiliated with the following schools: Yale University, University of Oxford, University of California, Los Angeles, Stanford University, National Taiwan University, University of California, San Francisco

Neil J. Risch's AcademicInfluence.com Rankings

Neil J. Risch

Biology

#3457

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#5287

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Genetics

#249

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#299

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Neil J. Risch

Mathematics

#3910

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#5654

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Statistics

#185

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#235

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mathematics Degrees

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Biology
Mathematics

Neil J. Risch's Degrees

PhD Biostatistics University of Washington
Masters Biostatistics University of Washington
Bachelors Mathematics University of California, Berkeley

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Neil J. Risch'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

The Future of Genetic Studies of Complex Human Diseases (1996) (5487)
A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis (1996) (3749)
Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis (1997) (3245)
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. (1997) (2488)
Searching for genetic determinants in the new millennium (2000) (1964)
Genetic heritability and shared environmental factors among twin pairs with autism. (2011) (1826)
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease (1994) (1772)
Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. (2009) (1704)
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease (2003) (1576)
Linkage strategies for genetically complex traits. I. Multilocus models. (1990) (1404)
Candidate-gene approaches for studying complex genetic traits: practical considerations (2002) (1117)
A comparison of linkage disequilibrium measures for fine-scale mapping. (1995) (1112)
Linkage strategies for genetically complex traits. II. The power of affected relative pairs. (1990) (1076)
The importance of race and ethnic background in biomedical research and clinical practice. (2003) (1041)
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein (1997) (994)
Genetic analysis of breast cancer in the cancer and steroid hormone study. (1991) (963)
Positional Cloning of the Human Quantitative Trait Locus Underlying Taste Sensitivity to Phenylthiocarbamide (2003) (813)
Categorization of humans in biomedical research: genes, race and disease (2002) (765)
A highly significant association between a COMT haplotype and schizophrenia. (2002) (715)
A genomic screen of autism: evidence for a multilocus etiology. (1999) (693)
The continuous performance test, identical pairs version (CPT-IP): I. new findings about sustained attention in normal families (1988) (678)
A genetic basis for familial aggregation in multiple sclerosis (1995) (674)
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. (2006) (663)
Autosomal dominant inheritance of early‐onset breast cancer. Implications for risk prediction (1994) (627)
A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 (1996) (608)
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins (1996) (579)
Assessing the role of HLA-linked and unlinked determinants of disease. (1987) (568)
Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. (2005) (564)
Extreme discordant sib pairs for mapping quantitative trait loci in humans. (1995) (551)
Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. (2001) (544)
Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. (1994) (528)
Twin concordance and sibling recurrence rates in multiple sclerosis (2003) (502)
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. (1990) (448)
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population (1995) (431)
Genetic linkage between X-chromosome markers and bipolar affective illness (1987) (406)
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling. (1998) (386)
Age at onset as an indicator of familial risk of breast cancer. (1990) (381)
Evidence for genetic basis of multiple sclerosis (1996) (377)
High-throughput genotyping with single nucleotide polymorphisms. (2001) (365)
The DYT1 phenotype and guidelines for diagnostic testing (2000) (358)
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus (1998) (351)
The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches. (2001) (342)
Latino populations: a unique opportunity for the study of race, genetics, and social environment in epidemiological research. (2005) (328)
Localization of a gene for partial epilepsy to chromosome 10q (1995) (326)
Co-morbidity and familial aggregation of alcoholism and anxiety disorders (1998) (308)
An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. (1993) (303)
Association between migraine and stroke in a large-scale epidemiological study of the United States. (1997) (298)
Genetic linkage and complex diseases, with special reference to psychiatric disorders (1990) (289)
A brief history of human disease genetics (2020) (288)
No association between an allele at the D2 dopamine receptor gene (DRD2) and alcoholism. (1991) (285)
The A1 allele at the D2 dopamine receptor gene and alcoholism. A reappraisal. (1993) (281)
Admixture mapping for hypertension loci with genome-scan markers (2005) (279)
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis (1995) (278)
Parent-of-origin effect in multiple sclerosis: observations in half-siblings (2004) (265)
Reconstructing genetic ancestry blocks in admixed individuals. (2006) (264)
Genomic Priorities and Public Health (2003) (263)
Male homosexuality: absence of linkage to microsatellite markers at Xq28. (1999) (250)
Human gene for torsion dystonia located on chromosome 9q32-q34 (1989) (249)
Spontaneous mutation and parental age in humans. (1987) (242)
Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort (2015) (241)
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. (2005) (240)
Statement on use of apolipoprotein E testing for Alzheimer disease. American College of Medical Genetics/American Society of Human Genetics Working Group on ApoE and Alzheimer disease. (1995) (238)
Population stratification confounds genetic association studies among Latinos (2005) (236)
Natural variation in human membrane transporter genes reveals evolutionary and functional constraints (2003) (236)
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation (2016) (233)
Immunology: Hepatitis A virus link to atopic disease (2003) (225)
Narcolepsy is strongly associated with the TCR alpha locus (2009) (219)
Affected‐sib‐pair interval mapping and exclusion for complex genetic traits: Sampling considerations (1996) (218)
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21 (1997) (216)
A manic depressive history (1996) (216)
Common variants in P2RY11 are associated with narcolepsy (2010) (213)
Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritance (1989) (210)
Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP). (2002) (202)
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. (2008) (201)
Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient. (2002) (200)
Estimating kinship in admixed populations. (2012) (199)
Comorbidity and co-transmission of alcoholism, anxiety and depression (1994) (195)
Model misspecification and multipoint linkage analysis. (1992) (194)
Genetic admixture and asthma‐related phenotypes in Mexican American and Puerto Rican asthmatics (2005) (191)
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array. (2011) (188)
A large electronic health record-based genome-wide study of serum lipids (2018) (188)
Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus (2009) (181)
Mapping quantitative trait loci with extreme discordant sib pairs: sampling considerations. (1996) (181)
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. (2013) (176)
A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate. (2002) (170)
Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q (1993) (166)
Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. (1992) (165)
Newborn Sequencing in Genomic Medicine and Public Health (2017) (163)
Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship. (1989) (159)
Familial aggregation of absolute pitch. (2000) (159)
Recent genetic selection in the ancestral admixture of Puerto Ricans. (2007) (158)
The calculation of breast cancer risk for women with a first degree family history of ovarian cancer (1993) (157)
Risk factors predicting the incidence of second primary breast cancer among women diagnosed with a first primary breast cancer. (1992) (156)
Will the genomics revolution revolutionize psychiatry? (2003) (156)
Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigrees (1993) (156)
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm. (2011) (152)
Migraine and depression: association and familial transmission. (1988) (151)
Bayesian analysis of haplotypes for linkage disequilibrium mapping. (2001) (151)
Genotyping Informatics and Quality Control for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort (2015) (150)
Intragenic Cis and Trans modification of genetic susceptibility in DYT1 torsion dystonia. (2007) (147)
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome (2003) (146)
Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups (2004) (146)
Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes (2001) (146)
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2017) (145)
Characterizing the admixed African ancestry of African Americans (2009) (143)
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34 (1990) (138)
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus (2007) (136)
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. II. Individual genotyping. (1999) (136)
No excess of homozygosity at loci used for DNA fingerprinting. (1990) (134)
Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection. (2003) (132)
Future of genetics of mood disorders research (2002) (131)
Statistical evaluation of multiple-locus linkage data in experimental species and its relevance to human studies: application to nonobese diabetic (NOD) mouse and human insulin-dependent diabetes mellitus (IDDM). (1993) (126)
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. (1992) (126)
Canadian Collaborative Project on Genetic Susceptibility to MS, Phase 2: Rationale and Method (1998) (125)
Familial recurrence of autism spectrum disorder: evaluating genetic and environmental contributions. (2014) (124)
The Association of Refractive Error with Glaucoma in a Multiethnic Population. (2016) (124)
The genetics of infantile hypertrophic pyloric stenosis. A reanalysis. (1993) (120)
Estimating genotype error rates from high-coverage next-generation sequence data (2014) (118)
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. (2013) (117)
A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. (2003) (117)
HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups. US Modafinil in Narcolepsy Multicenter Study Group. (1998) (116)
Automated Assay of Telomere Length Measurement and Informatics for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort (2015) (114)
Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group. (1996) (113)
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences. (2015) (113)
Genetic Contributors to Variation in Alcohol Consumption Vary by Race/Ethnicity in a Large Multi-Ethnic Genome-wide Association Study (2017) (111)
Segregation analysis incorporating linkage markers. I. Single-locus models with an application to type I diabetes. (1984) (111)
On the probability of matching DNA fingerprints. (1992) (109)
Relations of genetic and environmental factors in the etiology of epilepsy (1996) (107)
On the twin risk in autism. (2002) (106)
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci (2018) (106)
Segregation analysis of schizophrenia and related disorders. (1984) (104)
X‐linkage and genetic heterogeneity in bipolar‐related major affective illness: reanalysis of linkage data (1982) (103)
Gene loss and gain in the evolution of the vertebrates. (1994) (102)
A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci (2018) (99)
Diminished recall and the cohort effect of major depression: a simulation study (1994) (98)
Genetic linkage: interpreting lod scores. (1992) (98)
History Shaped the Geographic Distribution of Genomic Admixture on the Island of Puerto Rico (2011) (97)
A meta-analysis of genomic screens in multiple sclerosis. The Transatlantic Multiple Sclerosis Genetics Cooperative. (2001) (96)
Genome‐wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response (2015) (96)
Global transcriptional response to interferon is a determinant of HCV treatment outcome and is modified by race (2006) (95)
The genetic epidemiology of second primary breast cancer. (1992) (94)
Myoclonus dystonia (2002) (93)
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism (2004) (93)
Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients (2000) (93)
Disequilibrium mapping: composite likelihood for pairwise disequilibrium. (1996) (92)
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. (2018) (91)
Increased risk for recurrent major depression in DYT1 dystonia mutation carriers (2004) (91)
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. (1999) (91)
The role of exome sequencing in newborn screening for inborn errors of metabolism (2020) (89)
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. (2010) (89)
Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans (2006) (89)
A note on multiple testing procedures in linkage analysis. (1991) (87)
Ancestry-related assortative mating in Latino populations (2009) (85)
Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance. (1990) (85)
Haemochromatosis HFE and genetic complexity (1997) (84)
Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. (2014) (84)
Homozygosity and linkage disequilibrium. (2002) (79)
Diagnostic criteria for dystonia in DYT1 families (2002) (79)
Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis. (2001) (78)
Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region (2008) (78)
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure (2017) (78)
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records (2016) (77)
Narcolepsy is strongly associated with the T-cell receptor alpha locus (vol 41, pg 708, 2009) (2014) (76)
Myoclonus dystonia: Possible association with obsessive–compulsive disorder and alcohol dependence (2002) (76)
Searching for genes in complex diseases: lessons from systemic lupus erythematosus. (2000) (72)
Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish–Mennonites (2007) (70)
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. (1997) (69)
The relationship between maternal age and chromosome size in autosomal trisomy. (1986) (69)
Admixture mapping and the role of population structure for localizing disease genes. (2008) (68)
Ancestry-environment interactions and asthma risk among Puerto Ricans. (2006) (68)
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations. (2000) (68)
Clinical Indicators of Genetic Susceptibility to Epilepsy (1996) (67)
A study of idiopathic torsion dystonia in a non‐Jewish family (1994) (66)
A new statistical test for linkage heterogeneity. (1988) (66)
Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. (2001) (65)
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia. (1998) (65)
An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. (2004) (65)
Lack of association of the angiotensinogen‐6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program (2000) (65)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity (2019) (65)
Dissecting complex diseases in complex populations: asthma in latino americans. (2007) (63)
Ethnicity and human genetic linkage maps. (2005) (62)
Human genetic variation recognizes functional elements in noncoding sequence. (2010) (62)
Exclusion of the DYT1 locus in familial torticollis (1996) (62)
Austism and the X Chromosome: Multipoint sib-Pair Analysis (1996) (62)
Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. (2004) (61)
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes. (1996) (60)
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease (2008) (60)
A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins. (2003) (59)
Genetic variation in aldosterone synthase predicts plasma glucose levels (2001) (57)
Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations. (2000) (57)
Effect of age at onset and parental disease status on sibling risks for MS (1998) (57)
Implications of multilocus inheritance for gene-disease association studies. (2001) (57)
Forensic Inference from DNA Fingerprints (1992) (56)
Minimum incidence of primary cervical dystonia in a multiethnic health care population (2007) (55)
Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families. (2002) (55)
Tree-structured supervised learning and the genetics of hypertension. (2004) (55)
Functional genomics of membrane transporters in human populations. (2005) (55)
Age at onset in bipolar-related major affective illness: clinical and genetic implications. (1982) (54)
Postnatal Experiences and Genetic Effects on Squirrel Monkey Social Affinities and Emotional Distress (1999) (54)
Genetics of IDDM: Evidence for complex inheritance with HLA (1989) (54)
Statistical evaluation of DNA fingerprinting: a critique of the NRC's report. (1993) (53)
No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study (2002) (53)
The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese origin. (2001) (52)
Are generalized and localization-related epilepsies genetically distinct? (1998) (52)
Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7 (1995) (51)
Clinical-genetic spectrum of primary dystonia. (1998) (51)
The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family. (1998) (51)
Estimation of allele frequencies for VNTR loci. (1991) (51)
Evidence of reproductive stoppage in families with autism spectrum disorder: a large, population-based cohort study. (2014) (51)
The spectrum concept of schizophrenia: evidence for a genetic-environmental continuum. (1987) (49)
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer (2017) (48)
Ethnic differentiation at VNTR loci, with special reference to forensic applications. (1992) (47)
Linkage detection tests under heterogeneity (1989) (46)
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population (2004) (46)
The Epilepsy Phenome/Genome Project (2013) (45)
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease. (2008) (44)
Search for a founder mutation in idiopathic focal dystonia from Northern Germany. (1998) (43)
Exclusion of Linkage to the HLA Region in Ninety Multiplex Sibships with Autism (1999) (43)
Assessing the role of X-linked inheritance in bipolar-related major affective disorder. (1986) (41)
The impact of phenotypic variation on genetic analysis: application to X‐linkage in manic‐depressive illness (1990) (41)
Genetic variation in the human urea transporter-2 is associated with variation in blood pressure. (2001) (41)
Segregation analysis of human hand preference (1985) (40)
Birth Order Effects on Nonverbal IQ Scores in Autism Multiplex Families (2001) (40)
Response to Zhang et al. (2005) Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16 (2005) (39)
Corrections to "Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs". (1992) (38)
Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD (2008) (38)
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. (2019) (37)
Differences in Albuminuria Between Hispanics and Whites: An Evaluation by Genetic Ancestry and Country of Origin: The Multi-Ethnic Study of Atherosclerosis (2010) (37)
The Association of African Ancestry and Elevated Creatinine in the Coronary Artery Risk Development in Young Adults (CARDIA) Study (2009) (36)
Low-density lipoprotein cholesterol responsiveness to diet in normolipidemic subjects. (1993) (36)
Estimating morbidity risks in relatives: The effect of reduced fertility (1983) (36)
Admixture Mapping of Quantitative Trait Loci for BMI in African Americans: Evidence for Loci on Chromosomes 3q, 5q, and 15q (2009) (35)
Evolving methods in genetic epidemiology. II. Genetic linkage from an epidemiologic perspective. (1997) (35)
Male sexual orientation and genetic evidence. (1993) (35)
Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort (2015) (35)
A note on Hardy-Weinberg equilibrium of VNTR data by using the Federal Bureau of Investigation's fixed-bin method. (1992) (34)
Secondary dystonia and the DYTI gene (1997) (33)
Searching for susceptibility genes in schizophrenia by genetic linkage analysis. (1996) (33)
Estimation of morbid risk and age at onset with missing information. (1991) (33)
A genome-wide scan in forty large pedigrees with multiple sclerosis (2007) (32)
A multigenerational family with multiple sclerosis. (2002) (32)
Assessing the clinical impact of CYP2C9 pharmacogenetic variation on phenytoin prescribing practice and patient response in an integrated health system. (2019) (31)
Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results. (1997) (30)
Linkage and mode of inheritance in complex traits. (1989) (30)
Admixture mapping of quantitative trait loci for blood lipids in African-Americans. (2009) (29)
An autosomal genome-wide scan for loci linked to pre-diabetic phenotypes in nondiabetic Chinese subjects from the Stanford Asia-Pacific Program of Hypertension and Insulin Resistance Family Study. (2005) (29)
Differential fertility in bipolar affective illness. (1982) (28)
Genetic Analysis Workshop 7: summary of the melanoma workshop. (1992) (28)
Depression: A Meta-analysis ), Stressful Life Events, and Risk of 5-HTTLPR Interaction Between the Serotonin Transporter Gene ( (2009) (28)
Variants in CXADR and F2RL1 are associated with blood pressure and obesity in African-Americans in regions identified through admixture mapping (2012) (27)
Birth cohort and familial risk of epilepsy: the effect of diminished recall in studies of lifetime prevalence. (1995) (27)
Genetic analyses of complex behavioral disorders. (1997) (26)
Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African Americans in two large US cohorts. (2020) (26)
Genome-wide distribution of ancestry in Mexican Americans (2008) (25)
X-linkage in bipolar affective illness. Perspectives on genetic heterogeneity, pedigree analysis and the X-chromosome map. (1981) (24)
Common variants in P 2 RY 11 are associated with narcolepsy (2010) (24)
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative. (2014) (23)
Structured mating: Patterns and implications (2017) (22)
A genome scan in a single pedigree with a high prevalence of multiple sclerosis (2007) (22)
Genetic analysis of platelet monoamine oxidase activity in families of schizophrenic patients. (1985) (21)
Comments on the statistical aspects of the NRC's report on DNA typing. (1994) (21)
A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness (2020) (20)
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+ (2009) (20)
Ethnic variation in the clinical expression of idiopathic torsion dystonia (1997) (19)
EXOME SEQUENCING IN BIPOLAR DISORDER REVEALS SHARED RISK GENE AKAP11 WITH SCHIZOPHRENIA (2021) (19)
Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. (1995) (18)
Inheritance of idiopathic torsion dystonia among Ashkenazi Jews. (1988) (18)
Physical properties of VNTR data, and their impact on a test of allelic independence. (1993) (18)
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk (2020) (17)
Characterization of Statin Low-Density Lipoprotein Cholesterol Dose-Response Using Electronic Health Records in a Large Population-Based Cohort (2018) (17)
Linkage studies of psychiatric disorders (2005) (17)
Haplotype structure and ethnic-specific allele frequencies at the OCTN locus: implications for the genetics of Crohn's disease. (2005) (16)
Telomere length and socioeconomic status at neighborhood and individual levels among 80,000 adults in the Genetic Epidemiology Research on Adult Health and Aging cohort (2019) (16)
Molecular epidemiology of Tay-Sachs disease. (2001) (16)
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
The role of the DYT1 gene in secondary dystonia. (1998) (16)
Twins of mistaken zygosity (TOMZ): evidence for genetic contributions to dietary patterns and physiologic traits. (2006) (15)
A general model for disease‐marker association (1983) (15)
Differences in the Genetic Susceptibility to Age-Related Macular Degeneration Clinical Subtypes. (2015) (15)
The Fruitless Search for Genes in Psychiatry and Psychology: Time to Re-examine a Paradigm? (2010) (15)
Common coding variants in the HLA-DQB1 region confer susceptibility to age-related macular degeneration (2016) (14)
Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire (2018) (14)
An extremes of outcome strategy provides evidence for multiple sclerosis severity being determined by alleles at the HLA-DRB1 locus (2008) (13)
Genetic Epidemiology and Gene Discovery in Epilepsy (2012) (13)
Pierpont syndrome associated with the p.Tyr446Cys missense mutation in TBL1XR1. (2017) (13)
Genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches Cancer Epidemiol. Biomark (2002) (12)
Variants for HDL-C, LDL-C, and Triglycerides Identified from Admixture Mapping and Fine-Mapping Analysis in African American Families (2015) (12)
African American race but not genome-wide ancestry is negatively associated with atrial fibrillation among postmenopausal women in the Women's Health Initiative. (2013) (12)
A brief note on the resemblance between relatives in the presence of population stratification (2012) (12)
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility (2020) (12)
The DYT1 mutation and nonfamilial primary torsion dystonia. (2001) (11)
TCR beta polymorphisms and multiple sclerosis. (2004) (10)
Population genetics of the HRAS1 minisatellite locus. (1993) (10)
Response to Price et al. (2008) (10)
Genetics for the Human Race (2004) (9)
Feasibility of half‐sibling designs for detecting a genetic component to a disease (1994) (9)
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change (2020) (9)
Genetic analysis of the affective disorders: Summary of GAW5 (1989) (9)
Estimation of disease risk under bivariate models of multifactorial inheritance (1990) (9)
A unified framework identifies novel links between plasma lipids and diseases from electronic medical records across large-scale cohorts (2021) (9)
The effects of reduced fertility, method of ascertainment, and a second unlinked locus on affected sib-pair marker allele sharing. (1983) (9)
Effect of SLCO1B1 T521C on Statin‐Related Myotoxicity With Use of Lovastatin and Atorvastatin (2021) (8)
NRC report on DNA typing. (1993) (8)
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations (2018) (8)
A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X‐linked trichothiodystrophy (2019) (8)
Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study. (2006) (8)
P Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies (2010) (7)
TCR β polymorphisms and multiple sclerosis (2004) (7)
Genetic linkage and complex diseases: A response (1990) (7)
Developments in gene mapping with linkage methods. (1991) (7)
Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction (2020) (6)
Use of sibling risk ratios and components of genetic variance in the characterization of a simulated oligogenic disease (1995) (5)
Erratum: Common variants in P2RY11 are associated with narcolepsy (2011) (5)
143. Autism and the x-chromosome: Multipoint SIB pair analysis (1996) (5)
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change (2020) (5)
Genetic Concepts and Methods in Epidemiologic Research (2006) (5)
Genetic Data and the African Origin of Humans (1996) (5)
Dissecting Complex Diseases in Complex Populations (2012) (4)
Contribution to the pollination biology of Ophrys scolopax CAVANILLES (Orchidaceae) in southern France (2007) (4)
Selection in the Ashkenazi Jewish Population Unlikely—Reply to Zlotogora and Bach (2003) (4)
Alcoholism and the D2 Dopamine Receptor Gene-Reply (1993) (4)
The SNP Endgame: A Multidisciplinary Approach * (2005) (4)
Twins of Mistaken Zygosity (TOMZ): Evidence for Genetic Contributions to Dietary Patterns and Physiologic Traits (2006) (3)
Analysis of putative cis-regulatory elements regulating blood pressure variation (2019) (3)
Effects of Age and Ethnicity on the Link Between APOE ∊4 and Alzheimer Disease—Reply (1998) (3)
Evaluation of a susceptibility gene for schizophrenia on chromosome 6P (1996) (3)
Genetic analysis workshop II: Multiple‐locus segregation analysis incorporating linkage markers (1984) (3)
Dropped genetics paper lacked scientific merit (2002) (3)
Response:Interpretations of Multiregional Evolution (1996) (3)
Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations (2020) (3)
Early-Onset, Generalized Dystonia Caused by DYT1 Gene on Chromosome 9q34 (1995) (2)
The Genetic Epidemiology of Cancer (2001) (2)
Genetic Analysis of Complex Diseases (1997) (2)
Apolipoprotein E-e4 and apolipoprotein E-e2 are susceptibility genes that affect the rate of disease expressivity of late-onset familial and sporadic Alzheimer disease (1994) (2)
2004 Curt Stern Award Address. The SNP endgame: a multidisciplinary approach. (2005) (2)
Response: genetic data and the african origin of humans. (1996) (2)
Genetic susceptibility to multiple sclerosis (1995) (2)
X-linkage in affective and schizoaffective disorders: genetic and diagnostic implications. (1982) (2)
Response to the Letter "Gametic and Zygotic Associations" by Rong-Cai Yang (2003) (2)
A genome-scan in a single pedigree with a high prevalence of MS (2007) (2)
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci (2018) (2)
Gene-Environment Interactions and Depression—Reply (2009) (2)
S-55-1 Familial transmission of alcoholism and anxiety disorders (1996) (1)
Mo-P6:419 A common novel SNP in the peroxisome proliferative activated receptor gamma gene is associated with early-onset coronary artery disease (2006) (1)
Linkage Disequilibrium Analysis of the Gaucher Disease N370S Mutation (1999) (1)
Predicting the age of the mutation for Usher syndrome type I in the Acadian population (1994) (1)
Study of the genetically complex epilepsies (2010) (1)
Association Study of Over 200,000 Subjects Detects Novel Rare Variants, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility (2020) (1)
Setting priorities for genomic research [2] (multiple letters) (2004) (1)
Neighborhood Deprivation and Telomere Length (TL): The Genetic Epidemiology of Research In Aging (GERA) Cohort (2016) (1)
Inheritance of Primary Torsion Dystonia Among Ashkenazi Jews (1987) (1)
Sib‐pair analysis of the collaborative study on the genetics of alcoholism data set (1999) (1)
B4-4: Genome-Wide Association Study of Macular Degeneration: Early Results from the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) (2013) (1)
Un-kyung Kim Taste Sensitivity to Phenylthiocarbamide Positional Cloning of the Human Quantitative Trait Locus Underlying (2013) (0)
Genetic Diseases in the Jewish Population (2007) (0)
Title Genome-Wide Association Study Identifies ABCG 2 ( BCRP ) as an Allopurinol Transporter and a Determinant of Drug Response Permalink (2015) (0)
GENETIC ANCESTRY AND COUNTRY OF ORIGIN (2010) (0)
ELECTRONIC MEDICAL RECORD PHENOTYPES OF SUBJECTIVE MEMORY COMPLAINTS, ALZHEIMER’S DISEASE, DEMENTIA, AND MCI ARE INCREASED IN THOSE WITH APOE4: FINDINGS FROM THE RESEARCH PROGRAM ON GENES, ENVIRONMENT, AND HEALTH (2016) (0)
ABSTRACTS FROM THE TWENTY-SECOND ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY (2013) (0)
A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness (2020) (0)
Apolipoprotein E phenotype and dietary responsiveness in hyperlipidemic subjects (1994) (0)
National Institute on Aging Using Genome-Wide Association Studies ( GWAS ) to Explore Fundamental Questions About Aging in the Health and Retirement Study ( HRS ) Sample Summary of an Expert Meeting (2011) (0)
[Table, Table 1. Methods for Gene Identification in Genetically Complex Epilepsies] (2012) (0)
Genetic relationship between nevus count or nevus density and cutaneous malignant melanoma. (1992) (0)
Linkage analysis for autism and chromosomal markers located in the PWS/Angelman syndrome region (1997) (0)
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
Assessment of the Association between Environmental Justice Data for Air Pollution and Telomere Length (2018) (0)
Validation of Electronic Health Records for the Assessment of Statin Dosing In Research (2017) (0)
SU23 ASSOCIATIONS OF POLYGENIC RISK OF SCHIZOPHRENIA AND MAJOR DEPRESSION IN STUDIES OF BIPOLAR DISORDER AND MAJOR DEPRESSION (2019) (0)
Population Genetics of the HRAS I Minisatellite Locus (2006) (0)
Abstract P253: Genome-Wide Association Study of Electrocardiographic Left Ventricular Hypertrophy among Persons of European Ancestry: the Kaiser Permanente/UCSF GERA Cohort (2014) (0)
distributions—in terms of numbers, frequencies, ages, and geography—are consistent with genetic drift alone. (2003) (0)
Population-based Studies of Risk Factors in Autoimmunity: The Kaiser Permanente Autoimmune Disease Research Group (KPADRG) (2007) (0)
141 Linkage studies in schizophrenia and affecfive disorders in European populations (1997) (0)
PS3-15: Genome-Wide Association Study of Anxiety Disorders: Early Results from Kaiser Permanente’s Research Program on Genes, Environment, and Health (RPGEH) (2013) (0)
A brief history of human disease genetics (2020) (0)
Principles of molecular genetics/Dystonia (1992) (0)
Phenylthiocarbamide Locus Underlying Taste Sensitivity to Positional Cloning of the Human Quantitative Trait (2007) (0)
Response (1991) (0)
Torsade De Pointes: A Nested Case Control Study in an Integrated Health Care Delivery System (2020) (0)
Confirmation of linkage between the HLA-DR locus and multiple sclerosis in two unusually large MS families. (1999) (0)
Polygenic risk score and statin relative risk reduction for primary prevention in a real-world population (2021) (0)
Abstract 1316: Germline genetic signals across multiple aggressive prostate cancer phenotypes (2017) (0)
A genome-wide scan for regions shared identical by descent in Hutterite MS families (2002) (0)
' s response to reviews Title : Failure to replicate an association of SNPs in the oxidized LDL receptor gene ( OLR 1 ) with CAD (2008) (0)
Twenty second annual symposium on etiology, pathogenesis, and treatment of Parkinson's disease and other movement disorders (2008) (0)
CCR5 does not influence genetic susceptibility to multiple sclerosis in the Canadian population. (1999) (0)
Search for torsion dystonia gene (1995) (0)
Genome-wide Association Study Identifies ABCG2 (BCRP) as an Allopurinol Transporter and a Determinant of Drug Response Authors (2014) (0)
269 Genetic ancestry does not influence atopic dermatitis susceptibility or disease activity among African Americans (2018) (0)
Neil Risch noncoding sequence Human genetic variation recognizes functional elements in Material Supplemental (2010) (0)
Genetic analysis of vitamin D pathway genes in multiple sclerosis (1999) (0)
33 INVESTIGATING RARE PATHOGENIC/LIKELY PATHOGENIC EXONIC VARIATION IN 3,987 BIPOLAR PATIENTS (2019) (0)
Contributors and Participants (1982) (0)
Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos (2017) (0)
EFFECTS OF AGE AND ETHNICITY ON THE LINK BETWEEN APOE EPSILON 4 AND ALZHEIMER DISEASE. AUTHORS' REPLY (1998) (0)
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure (2017) (0)
Protein-6 and Coronary Artery Disease in 19 Case-Control Studies Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like (2012) (0)
Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control (2017) (0)
2015 ASHG Awards and Addresses. (2016) (0)
Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR (1992) (0)
The most recent and extensive genome-wide human genetic linkage maps (2005) (0)
Forty multiplex families with MS: Linkage analysis of chromosome 6 and HLA-DRB1 (2002) (0)
Abstract 1297: Genetic reclassification of prostate-specific antigen levels for personalized prostate cancer screening (2017) (0)
Polymorphisms High-Throughput Genotyping with Single Nucleotide Material (2001) (0)
A model system for identifying genes underlying complex traits. (2003) (0)
1027 Diagnostic yield of exome sequencing in prenatal diagnosis (2021) (0)
OA04.06 Examining Pleiotropic Associations of Genetic Risk Variants for Chronic Obstructive Pulmonary Disease with Lung Cancer Risk (2017) (0)
Multipoint sib pair analysis between X-chromosomal markers and autism (1995) (0)

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