Joseph Terwilliger | Academic Influence

Joseph Terwilliger's AcademicInfluence.com Rankings

Joseph Terwilliger

Biology

#7871

World Rank

#10858

Historical Rank

#2267

USA Rank

Genetics

#767

World Rank

#859

Historical Rank

#245

USA Rank

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Biology

Joseph Terwilliger's Degrees

PhD Genetics Columbia University
Bachelors Biology University of California, San Diego

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Why Is Joseph Terwilliger Influential?

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According to Wikipedia, Joseph Douglas Terwilliger is an American geneticist and professor of neurobiology at the Columbia University Medical Center and the New York State Psychiatric Institute. In addition to his scientific research, he is known for accompanying retired basketball player Dennis Rodman on his visits to North Korea, where he has said that he serves as Rodman's translator. He began his involvement in Rodman's trips to the country after winning a basketball game with him at an auction.

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Joseph Terwilliger'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

Handbook of Human Genetic Linkage (1994) (1062)
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome (1989) (864)
Identification of a variant associated with adult-type hypolactasia (2002) (825)
Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. (2001) (744)
Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12 (1996) (740)
Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis. (1997) (531)
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. (1992) (520)
How many diseases does it take to map a gene with SNPs? (2000) (515)
Large upward bias in estimation of locus-specific effects from genomewide scans. (2001) (491)
A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. (1995) (474)
Linkage disequilibrium mapping of complex disease: fantasy or reality? (1998) (388)
Candidate Endophenotypes for Genetic Studies of Suicidal Behavior (2009) (356)
Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (346)
Genomewide scan of multiple sclerosis in Finnish multiplex families. (1997) (321)
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. (1999) (294)
Linkage of familial combined hyperlipidaemia to chromosome 1q21–q23 (1998) (286)
A genomewide screen of 345 families for autism-susceptibility loci. (2003) (285)
A putative vulnerability locus to multiple sclerosis maps to 5p14–p12 in a region syntenic to the murine locus Eae2 (1996) (231)
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q (1995) (216)
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22. (2000) (215)
A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2q. (2000) (207)
Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified. (2000) (200)
Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. (1997) (191)
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. (2000) (184)
Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. (1993) (178)
A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2. (2000) (177)
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension. (1999) (177)
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q. (2001) (174)
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans. (2007) (167)
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. (1999) (164)
A radiation hybrid map of 506 STS markers spanning human chromosome 11 (1994) (163)
Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion (1998) (161)
An utter refutation of the ‘Fundamental Theorem of the HapMap’ (2006) (155)
True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. (1997) (153)
The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories. (2003) (141)
Genome‐wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings (2000) (139)
Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q. (1999) (138)
Gene Mapping in the 20th and 21st Centuries: Statistical Methods, Data Analysis, and Experimental Design (2010) (136)
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree. (1995) (135)
Schizophrenia in the genetic isolate of Finland. (1997) (133)
Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population. (1998) (125)
Chromosome‐based method for rapid computer simulation in human genetic linkage analysis (1993) (124)
Genomewide linkage analysis of celiac disease in Finnish families. (2002) (121)
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. (1999) (115)
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus. (1995) (111)
Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura (2006) (111)
Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters. (2000) (108)
A bias-ed assessment of the use of SNPs in human complex traits. (2002) (101)
Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes. (2000) (98)
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. (1992) (95)
An Association Analysis of Circadian Genes in Anxiety Disorders (2010) (93)
Confounding, ascertainment bias, and the blind quest for a genetic ‘fountain of youth’ (2003) (88)
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. (2007) (87)
Assessment of the Neuropeptide S System in Anxiety Disorders (2010) (87)
Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions. (2000) (85)
New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105. (1995) (85)
Trait components provide tools to dissect the genetic susceptibility of migraine. (2006) (82)
Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set (1998) (79)
Genetic Variation and Human Disease: Principles and Evolutionary Approaches (1997) (78)
Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo (2000) (77)
Two-locus linkage analysis in multiple sclerosis (MS). (1994) (63)
Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1. (1995) (63)
An Association Analysis of Murine Anxiety Genes in Humans Implicates Novel Candidate Genes for Anxiety Disorders (2008) (61)
Fine mapping of the SLEB2 locus involved in susceptibility to systemic lupus erythematosus. (2000) (59)
Prostatic intraepithelial neoplasia and adenocarcinoma in mice expressing a probasin-Neu oncogenic transgene. (2006) (59)
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus. (1990) (58)
Gene Mapping in the 20th and 21st Centuries: Statistical Methods, Data Analysis, and Experimental Design (2009) (58)
ForSim: a tool for exploring the genetic architecture of complex traits with controlled truth (2008) (54)
A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22. (2001) (53)
Consistently replicating locus linked to migraine on 10q22-q23. (2008) (51)
Glaucomatous Optic Neuropathy Associated with Nocturnal Dip in Blood Pressure: Findings from the Maracaibo Aging Study. (2018) (48)
DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrence. (1995) (47)
On the resolution and feasibility of genome scanning approaches. (2001) (45)
Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1 (1999) (44)
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21 (2001) (43)
PSEUDOMARKER: A Powerful Program for Joint Linkage and/or Linkage Disequilibrium Analysis on Mixtures of Singletons and Related Individuals (2011) (43)
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13. (1998) (43)
A novel polylocus method for linkage analysis using the lod‐score or affected sib‐pair method (1993) (39)
AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis. (2005) (38)
Identification of a Potential Susceptibility Locus for Macular Telangiectasia Type 2 (2012) (35)
On the relative importance of marker heterozygosity and intermarker distance in gene mapping. (1992) (35)
GAW12: Simulated Genome Scan, Sequence, and Family Data for a Common Disease (2001) (33)
Incidence of dementia in elderly Latin Americans: Results of the Maracaibo Aging Study (2018) (30)
Genome-wide scan for schizophrenia in the Finnish population : evidence for a locus on chromosome 7 q 22 (2000) (27)
Cystathionine beta‐synthase deficiency in Central Europe: Discrepancy between biochemical and molecular genetic screening for homocystinuric alleles (2001) (27)
PSEUDOMARKER 2.0: efficient computation of likelihoods using NOMAD (2014) (26)
Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individuals (2019) (24)
Molecular Pathways Mediating Immunosuppression in Response to Prolonged Intensive Physical Training, Low-Energy Availability, and Intensive Weight Loss (2019) (23)
A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions. (1992) (22)
Assessing the Evidence for Linkage in Psychiatric Genetics (1992) (20)
A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm (2012) (18)
Risk Factors for Orthostatic Hypotension: Differences Between Elderly Men and Women (2018) (18)
Linkage analysis of schizophrenia controlling for population substructure (2009) (18)
On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case–control samples (2011) (17)
Concordance for sex and the pseudoautosomal gene hypothesis revisited: no evidence of increased sex concordance in a nationwide Finnish sample of siblings with paternally derived schizophrenia. (1998) (17)
Data simulation for GAW9 problems 1 and 2 (1995) (17)
No Genetic Linkage Detected for Schizophrenia to Xq27–q28 (1991) (16)
A likelihood-based extended admixture model of oligogenic inheritance in ‘model-based’ and ‘model-free’ analysis (2000) (15)
Reply to Sham et al. (1996) (12)
The PD-1 gene is associated with nephritis in human systemic lupus erythematosus (2000) (11)
Inflated false-positive rates in Hardy-Weinberg and linkage-equilibrium tests are due to sampling on the basis of rare familial phenotypes in finite populations. (2000) (11)
Update to Terwilliger and Göring's “Gene Mapping in the 20th and 21st Centuries” (2000): Gene Mapping When Rare Variants Are Common and Common Variants Are Rare (2009) (11)
Subject Index, Vol. 42, 1992 (1992) (11)
Optic neuropathy and congenital glaucoma associated with probable Zika virus infection in Venezuelan patients (2018) (11)
Non-congenital severe ocular complications of Zika virus infection (2018) (10)
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. (1991) (10)
Evidence for a susceptibility locus for manic-depressive disorder in Xq26 (1994) (9)
Evolution of the Simulated Data Problem (2001) (6)
On the Validity of the Likelihood Ratio Test and Consistency of Resulting Parameter Estimates in Joint Linkage and Linkage Disequilibrium Analysis under Improperly Specified Parametric Models (2012) (5)
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes risk. (2019) (4)
Linkage Analysis, Model‐Based (2005) (4)
Anthropological Genetics: Natural Experiments in Human Gene Mapping: The Intersection of Anthropological Genetics and Genetic Epidemiology (2006) (4)
OPEN-ANGLE GLAUCOMATOUS OPTIC NEUROPATHY IS RELATED TO DIPS RATHER THAN INCREASES IN THE MEAN ARTERIAL PRESSURE OVER 24-H (2022) (3)
Normal-tension glaucomatous optic neuropathy is related to blood pressure variability in the Maracaibo Aging Study (2021) (3)
Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement: Clinical, Pathological, and Genetic Features (1999) (3)
Capacity building for dealing with dementia in developing countries: Lessons from the Maracaibo Aging Study (2012) (2)
AUTOGSCAN: Powerful Tools for Automated Genome-Wide Linkage and Linkage Disequilibrium Analysis (2005) (2)
Fine mapping of a second locus involved in susceptibility for systemic lupus erythematosus on chromosome 4p in Icelandic pedigrees (2000) (2)
Correction: Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (2)
A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate (2016) (1)
Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins (2022) (1)
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27 (1991) (1)
Linkage analysis, model based† (2014) (1)
An X-chromosomal locus predisposing to bipolar disorder in an extended Finnish pedigree (1995) (1)
Whole-Genome Sequencing and Genomic Variant Analysis of Kazakh Individuals (2022) (1)
Science and Engineering and Their Different Roles in Investigations of the Genetic Portion of the Etiology of Complex Human Traits (2004) (1)
Reply to Deng and Chen (2000) (1)
Corrigendum: Optic neuropathy and congenital glaucoma associated with probable Zika virus infection in Venezuelan patients (2018) (1)
Hereditary motor and sensory neuropathy with proximal dominant involvement: clinical, pathological, and genetic features. (1999) (1)
Nighttime Blood Pressure Interacts with APOE Genotype to Increase the Risk of Incident Dementia of the Alzheimer's Type in Hispanics. (2020) (1)
PSEUDOMARKER 2.0: efficient computation of likelihoods using NOMAD (2014) (1)
A powerful one degree of freedom approach to mapping genes with linkage disequilibrium (1994) (0)
Subclinical Magnetic Resonance Imaging Markers of Cerebral Small Vessel Disease in Relation to Office and Ambulatory Blood Pressure Measurements (2022) (0)
Titre : Title : PSEUDOMARKER 2 . 0 : efficient computation of likelihoods using NOMAD Auteurs : (2019) (0)
Analysis of the hSLE1 locus on chromosome 2q37 in Mexican multicase families (2000) (0)
Contents, Vol. 42, 1992 (1992) (0)
Contributors and Participants (1982) (0)
Searching schizophrenia loci in a genetic isolate (1996) (0)
Study Design for Gene Mapping: Korean Migration History as a Natural Experiment to Study Gene-environment Interaction in Man (2004) (0)
On Inferior Power of Recently Developed Family-Based Association Analysis Methods for Next-Generation Sequencing Studies of Rare-Variants (2016) (0)
WHITE MATTER HYPERINTENSITIES IN LATIN AMERICANS: FINDINGS FROM THE MARACAIBO AGING STUDY (2018) (0)
Cognitive Domains in Low Literacy Populations: The Experience of the Maracaibo Aging Study (2021) (0)
SUBCLINICAL MAGNETIC RESONANCE IMAGING MARKERS OF CEREBRAL SMALL VESSEL DISEASE IN RELATION TO AMBULATORY BLOOD PRESSURE MEASUREMENTS (2022) (0)
Research on aging during the Venezuelan humanitarian crisis: the experience of the Maracaibo aging study (2021) (0)
GENETIC VARIANTS, METABOLOME, AND GUT MICROBIOME BIOMARKERS FOR OBESITY AND AGING IN RANDOMLY SELECTED KAZAKH INDIVIDUALS (2020) (0)
A LONGITUDINAL STUDY OF MID-TO LATE-LIFE BLOOD PRESSURE PROFILES AS RISK FACTORS FOR ALZHEIMER'S DISEASE IN HISPANICS (2018) (0)
BLOOD PRESSURE INDICES ARE ASSOCIATED WITH INCREASED REDUCED HIPPOCAMPAL VOLUME AND WHITE MATTER HYPERINTENSITIES IN HISPANIC ADULTS: THE MARACAIBO AGING STUDY (2016) (0)
INCIDENCE OF ALZHEIMER’S DISEASE IN HISPANICS: ROLE OF APOLIPOPROTEIN E GENOTYPES AND AMBULATORY BLOOD PRESSURE MONITORING (2018) (0)
Contents Vol. 71, 2011 (2011) (0)
Abstract WP138: Intracranial Artery Stenosis In Relation To Blood Pressure Components (2023) (0)
49-2 Loci on chromosomes 3p, 6p, and 8p do not contribute to schizophrenia in a Finnish family sample (1997) (0)
OPEN-ANGLE GLAUCOMATOUS OPTIC NEUROPATHY IS RELATED TO DIPS RATHER THAN INCREASES IN THE MEAN ARTERIAL PRESSURE OVER 24-H. (2022) (0)
Heritability of Ocular Traits in Hispanics: Findings from the Maracaibo Aging Study (2018) (0)
RandomSearchforSharedChromosomalRegions inFour Affected Individuals: TheAssignment ofa New Hereditary AtaxiaLocus (1995) (0)
Cerebral small vessel diseases are better associated with ambulatory than office blood pressure measurements (2020) (0)
Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individuals (2019) (0)
A17443 Ambulatory Blood Pressure Variability and Glaucomatous Optic Neuropathy: Findings from the Maracaibo Aging Study (2018) (0)
.8-Mb YAC Contig of Xq 1 3.1 (2007) (0)

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