Tara Matise

Q: What Schools Are Affiliated With Tara Matise

Tara Matise is affiliated with the following schools: Rutgers University, Cornell University, University of Washington

Tara Matise's AcademicInfluence.com Rankings

Tara Matise

Biology

#9197

World Rank

#12371

Historical Rank

Genetics

#958

World Rank

#1054

Historical Rank

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Biology

Why Is Tara Matise Influential?

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According to Wikipedia, Tara Matise is an American geneticist at Rutgers University. Since 2018, she has served as chair of the Department of Genetics. Her research interests span computational genetics, data science, and human genetics. She is co-director of the Rutgers University Genetics Coordinating Center.

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Tara Matise'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

Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
A Gene Map of the Human Genome (1996) (1080)
A physical map of 30,000 human genes. (1998) (670)
Genetic analyses of diverse populations improves discovery for complex traits (2019) (501)
Widespread RNA editing of embedded alu elements in the human transcriptome. (2004) (474)
Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map (1994) (407)
A second-generation combined linkage physical map of the human genome. (2007) (320)
A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4 (2001) (304)
NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees. (1998) (274)
Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium. (1998) (274)
Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. (1998) (248)
A combined linkage-physical map of the human genome. (2004) (246)
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. (1994) (244)
Age-related macular degeneration--a genome scan in extended families. (2003) (216)
Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study (2013) (212)
A high-density integrated genetic linkage and radiation hybrid map of the laboratory rat. (1999) (195)
Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. (1996) (175)
The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study (2011) (158)
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10 (1993) (154)
Phenome-Wide Association Study (PheWAS) for Detection of Pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network (2013) (152)
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects (2018) (143)
Insights into genetics, human biology and disease gleaned from family based genomic studies (2019) (135)
A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. (2003) (120)
Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained (2013) (116)
Erratum: Automated construction of genetic linkage maps using an expert system (MultiMap): A human genome linkage map (Nature Genetics (1994) 6 (384- 390)) (1994) (107)
An integrated genetic linkage map of the laboratory rat (1998) (97)
Construction of a 5000rad whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11 (2002) (88)
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome. (2003) (86)
Mapping and characterization of structural variation in 17,795 human genomes (2020) (84)
Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study. (2013) (82)
A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study (2013) (80)
Report of the second international workshop on human chromosome 1 mapping 1995. (1996) (78)
Nucleotide Sequence Database Policies (2002) (77)
A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2. (1995) (76)
Fine Mapping and Identification of BMI Loci in African Americans. (2013) (75)
A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM. (1993) (74)
Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study (2012) (72)
Preliminary Localization of a Gene for Autosomal Dominant Hypoparathyroidism to Chromosome 3ql3 (1994) (71)
Genome-wide search for schizophrenia susceptibility loci: the NIMH Genetics Initiative and Millennium Consortium. (1998) (70)
Loss of heterozygosity for chromosome 14q in neuroblastoma. (2001) (64)
Detailed molecular analysis of 1p36 in neuroblastoma. (2001) (62)
Report of the fifth international workshop on human chromosome 1 mapping 1999 (1997) (58)
Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study. (2014) (57)
Genotype Imputation of MetabochipSNPs Using a Study‐Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women's Health Initiative (2012) (57)
Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array (2016) (55)
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project (2013) (41)
Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study (2013) (39)
An integrated transcript map of human chromosome 1p35-p36. (1997) (38)
Cognitive Traits Link to Human Chromosomal Regions (2006) (37)
Contrasting methods of quantifying fine structure of human recombination. (2010) (37)
When a Case Is Not a Case: Effects of Phenotype Misclassification on Power and Sample Size Requirements for the Transmission Disequilibrium Test with Affected Child Trios (2009) (35)
MAP-O-MAT: internet-based linkage mapping (2005) (35)
The Influence of Obesity-Related Single Nucleotide Polymorphisms on BMI Across the Life Course (2013) (34)
Report of the first international workshop on human chomosome 1 mapping 1994 (1994) (32)
The PAGE Study: How Genetic Diversity Improves Our Understanding of the Architecture of Complex Traits (2018) (30)
Localizing the X-linked orange colour phenotype using feline resource families. (2005) (29)
Genotype Imputation of Metabochip SNPs Using a Study-Specific Reference Panel of ~4,000 Haplotypes in African Americans From the Women’s Health Initiative (2012) (28)
Association of Cancer Susceptibility Variants with Risk of Multiple Primary Cancers: The Population Architecture using Genomics and Epidemiology Study (2014) (28)
Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits (2017) (26)
The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE. (2019) (26)
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci (2017) (25)
The map problem: a comparison of genetic and sequence-based physical maps. (2002) (25)
Associations Between Incident Ischemic Stroke Events and Stroke and Cardiovascular Disease-Related Genome-Wide Association Studies Single Nucleotide Polymorphisms in the Population Architecture Using Genomics and Epidemiology Study (2012) (25)
Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study. (2013) (25)
The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis (2018) (24)
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study (2019) (23)
The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation. (2015) (22)
Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study (2013) (22)
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium (2017) (22)
Mapping and characterization of structural variation in 17,795 deeply sequenced human genomes (2018) (22)
Detection of tandem duplications and implications for linkage analysis. (1994) (22)
Pleiotropic and Sex-Specific Effects of Cancer GWAS SNPs on Melanoma Risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study (2015) (21)
Age-related Macular Degeneration Clinical Features in a Large Family and Linkage to Chromosome 1 q (2000) (21)
Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion. (1999) (20)
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994. (1994) (19)
Pleiotropy of Cancer Susceptibility Variants on the Risk of Non-Hodgkin Lymphoma: The PAGE Consortium (2014) (19)
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. (1995) (18)
Systematic evaluation of map quality: human chromosome 22. (2002) (18)
Centers for Mendelian Genomics: A decade of facilitating gene discovery (2021) (18)
A novel method for analyzing genetic association with longitudinal phenotypes (2013) (17)
MultiMap: An Expert System for Automated Genetic Linkage Mapping (1993) (17)
Genetic risk factors for BMI and obesity in an ethnically diverse population (2012) (16)
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations (2016) (15)
An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder (1997) (13)
A comprehensive view of human chromosome 1. (1999) (12)
Enabling Data and Compute Intensive Workflows in Bioinformatics (2011) (12)
Parallel computation of genetic likelihoods using CRI-MAP, PVM, and a network of distributed workstations. (1994) (12)
A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans (2019) (12)
Corrigendum: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map (1994) (12)
Report and abstracts of the third international workshop on human chromosome 1 mapping 1997. (1997) (12)
A radiation hybrid map of 95 STSs spanning human chromosome 13q. (1995) (10)
Single-Variant and Multi-Variant Trend Tests for Genetic Association with Next-Generation Sequencing That Are Robust to Sequencing Error (2013) (9)
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome (2020) (9)
Enhanced genetic maps from family-based disease studies: population-specific comparisons (2011) (8)
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome (2022) (7)
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities (2014) (6)
Map Error Reduction: Using Genetic and Sequence-Based Physical Maps to Order Closely Linked Markers (2002) (5)
Detecting heterogeneity with the affected‐pedigree‐member (APM) method (1993) (5)
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study (2020) (5)
Genome scanning for complex disease genes using the transmission/disequilibrium test and haplotype‐based haplotype relative risk (1995) (4)
Genomic mapping and mapping databases. (2001) (3)
Transmission disequilibrium test power and sample size in the presence of locus heterogeneity. (2009) (3)
Age-related Macular Degeneration: A Genome-wide Scan in Extended Families (2003) (3)
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits. (2022) (3)
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study (2021) (3)
A high-resolution human SNP linkage map (2002) (2)
Redefining replication in multi-ancestry genome-wide association (2021) (2)
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods (2004) (2)
Genome-Wide Epistatic Interaction between DEF1B and APOL1 High-Risk Genotypes for Chronic Kidney Disease. (2022) (1)
Meeting report. Statistical methods in genetic mapping. (1996) (1)
Report and abstracts of the Third International Workshop on Human Chromosome 13 Mapping. Tarrytown, New York, October 29-31, 1995. (1996) (1)
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods (1995) (1)
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI (2022) (1)
Lipid loci with multiple signals in Europeans. (2013) (0)
198-LB: Pleiotropy Analysis of Adiposity, Glycemic, and Renal Traits in the Population Architecture Using Genomics in Epidemiology (PAGE) Consortium (2020) (0)
Chromosome 13 and chromosome 2 (CA)n polymorphisms. (1994) (0)
Revised guidelines for authors of gene mapping reports (2000) (0)
Abstract 1662: Pleiotropic effects on lung cancer of genetic susceptibility variants identified for other malignancies: The Population Architecture using Genomics and Epidemiology Study (2012) (0)
Primary Cancers: The Population Architecture using Genomics Association of Cancer Susceptibility Variants with Risk of Multiple (2014) (0)
Mapping and characterization of structural variation in 17,795 human genomes (2020) (0)
Contents Vol. 74, 2012 (2013) (0)
Abstract P101: MEGA Analysis of Alcohol Consumption: The PAGE Study (2017) (0)
Abstract 051: Trans-ethnic Metabochip Genotyping of Established Lipid Loci Identifies Low Frequency Susceptibility Variants and Additional Independent Signals in Known Loci (2012) (0)
Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium (2017) (0)
Map of the Laboratory Rat A High-Density Integrated Genetic Linkage and Radiation Hybrid (1999) (0)
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects (2018) (0)
Subject Index Vol. 87, 1999 (2000) (0)
Contents Vol. 67, 2009 (2009) (0)
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci (2017) (0)
Genetic analyses of diverse populations improves discovery for complex traits (2019) (0)
Subject Index Vol. 67, 2009 (2009) (0)
Insights into genetics, human biology and disease gleaned from family based genomic studies (2019) (0)
The mouse rumpshaker mutation of the proteolipid protein in human X-linked recessive spastic paraplegia (1994) (0)
Contents Vol. 87, 1999 (2000) (0)

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What Schools Are Affiliated With Tara Matise?

Tara Matise is affiliated with the following schools: