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Author Details
Full Name
Jennifer E Below
Affiliation
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
ORCID
Career Start Year
2007
Papers
85
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36413071
IMMerge: merging imputation data at scale.
Bioinformatics
2023
36413071
IMMerge: merging imputation data at scale.
Bioinformatics
2023
37653519
Sex-specific associations between adipokine profiles and carotid-intima media thickness in the Cameron County Hispanic Cohort (CCHC).
Cardiovasc Diabetol
2023
36718543
Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.
Ann N Y Acad Sci
2023
37148359
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
Diabetologia
2023
36747740
Genome-wide association study identifies novel risk loci for apical periodontitis.
Res Sq
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
37051669
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease.
Alzheimers Dement
2023
37528943
Challenges and strategies for recruitment of minorities to clinical research and trials.
J Clin Transl Sci
2023
37499862
Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis.
J Endod
2023
37163006
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.
medRxiv
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
37528943
Challenges and strategies for recruitment of minorities to clinical research and trials.
J Clin Transl Sci
2023
37653519
Sex-specific associations between adipokine profiles and carotid-intima media thickness in the Cameron County Hispanic Cohort (CCHC).
Cardiovasc Diabetol
2023
37499862
Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis.
J Endod
2023
37051669
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease.
Alzheimers Dement
2023
37148359
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
Diabetologia
2023
37034649
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
2023
37163006
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.
medRxiv
2023
36718543
Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.
Ann N Y Acad Sci
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36747740
Genome-wide association study identifies novel risk loci for apical periodontitis.
Res Sq
2023
34788810
Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.
Hum Mol Genet
2022
35393509
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Commun Biol
2022
35513483
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Commun Biol
2022
36088317
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.
BMC Med Genomics
2022
35379992
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Nat Genet
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
36268164
Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.
HGG Adv
2022
35399580
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.
HGG Adv
2022
36580336
Association of Developmental Language Disorder With Comorbid Developmental Conditions Using Algorithmic Phenotyping.
JAMA Netw Open
2022
34788810
Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.
Hum Mol Genet
2022
34951656
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia
2022
35221896
Test of Prosody via Syllable Emphasis ("TOPsy"): Psychometric Validation of a Brief Scalable Test of Lexical Stress Perception.
Front Neurosci
2022
35157052
Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.
Hum Mol Genet
2022
35551307
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
2022
35379992
New insights into the genetic etiology of Alzheimer's disease and related dementias.
Nat Genet
2022
35399580
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.
HGG Adv
2022
35393509
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Commun Biol
2022
35513483
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Commun Biol
2022
36580336
Association of Developmental Language Disorder With Comorbid Developmental Conditions Using Algorithmic Phenotyping.
JAMA Netw Open
2022
36268164
Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.
HGG Adv
2022
36088317
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.
BMC Med Genomics
2022
34951656
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia
2022
35221896
Test of Prosody via Syllable Emphasis ("TOPsy"): Psychometric Validation of a Brief Scalable Test of Lexical Stress Perception.
Front Neurosci
2022
35157052
Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.
Hum Mol Genet
2022
33386679
Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta).
Mol Ecol Resour
2021
34165540
Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.
Hum Mol Genet
2021
33894541
Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier.
J Fluency Disord
2021
34032508
Revisiting Some Useful Statistical Guidelines in <i>Circulation Research</i> in Response to a Changing Landscape.
Circ Res
2021
1 - 50 of 170
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John C Chambers
Lee Kong Chian School of Medicine, Nanyang Technological University
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Mark I McCarthy
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