Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

Ginger A. Metcalf · SciRah

Researcher profile · Semantic Scholar

Ginger A. Metcalf

Share profile

Ginger A. Metcalf — researcher profile on SciRah

h-index: 27
Works: 83
Citations: 8,039

Most-cited papers

Somatic mutations affect key pathways in lung adenocarcinoma
L. Ding, G. Getz, D. Wheeler, E. Mardis +86 more
2008Nature2,758 citations Open access
Semantic Scholar
Temporal development of the gut microbiome in early childhood from the TEDDY study
C. Stewart, N. Ajami, Jacqueline L. O’Brien, D. Hutchinson +22 more
2018Nature1,765 citations Open access
Semantic Scholar
The gut mycobiome of the Human Microbiome Project healthy cohort
A. Nash, T. Auchtung, M. Wong, Daniel Patrick Smith +8 more
2017Microbiome868 citations Open access
Semantic Scholar
High-depth African genomes inform human migration and health
A. Choudhury, S. Aron, Laura R. Botigué, Dhriti Sengupta +28 more
2020Nature317 citations Open access
Semantic Scholar
Truvari: refined structural variant comparison preserves allelic diversity
A. English, Vipin K. Menon, R. Gibbs, Ginger A. Metcalf +1 more
2022bioRxiv230 citations Open access
Semantic Scholar
Additional file 11: Table S8. of Structure and function of the healthy pre-adolescent pediatric gut microbiome
E. Hollister, Kevin P. Riehle, R. Luna, Erica M. Weidler +10 more
2015218 citations
Semantic Scholar
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
J. Wessel, Audrey Y. Chu, Sara M. Willems, Shuai Wang +230 more
2015Nature Communications208 citations Open access
Semantic Scholar
Transmission event of SARS-CoV-2 delta variant reveals multiple vaccine breakthrough infections
Timothy Farinholt, H. Doddapaneni, X. Qin, Vipin K. Menon +11 more
2021BMC Medicine179 citations Open access
Semantic Scholar
Clonal hematopoiesis and risk of chronic liver disease
Wai-Hay J. Wong, C. Emdin, A. Bick, S. Zekavat +435 more
2023Nature174 citations Open access
Semantic Scholar
Structure and function of the healthy pre-adolescent pediatric gut microbiome
E. Hollister, Kevin P. Riehle, R. Luna, Erica M. Weidler +10 more
2015Microbiome143 citations Open access
Semantic Scholar
Unveiling microbial diversity: harnessing long-read sequencing technology
D. Agustinho, Yi-Lei Fu, Vipin K. Menon, Ginger A. Metcalf +2 more
2024Nature Methods106 citations
Semantic Scholar
Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome
E. Hollister, N. Oezguen, B. Chumpitazi, R. Luna +14 more
2019Journal of Molecular Diagnostics76 citations Open access
Semantic Scholar
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D. Rosen, Quan Sun, Jiawen Chen +21 more
2022American Journal of Human Genetics74 citations Open access
Semantic Scholar
Loss-of-function variants influence the human serum metabolome
Bing Yu, Alexander Hanbo Li, Ginger A. Metcalf, D. Muzny +5 more
2016Science Advances57 citations Open access
Semantic Scholar
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole-genome sequencing studies
Xi-Hao Li, Corbin Quick, Hufeng Zhou, Sheila M. Gaynor +420 more
2022Nature Genetics55 citations Open access
Semantic Scholar
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease
Alexander Hanbo Li, A. Morrison, C. Kovar, L. Cupples +11 more
2015Nature Genetics51 citations Open access
Semantic Scholar
Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.
A. Morrison, Zhuoyi Huang, Bing Yu, Ginger A. Metcalf +9 more
2017American Journal of Human Genetics49 citations Open access
Semantic Scholar
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
E. Venner, D. Muzny, Joshua D. Smith, K. Walker +17 more
2022Genome Medicine47 citations Open access
Semantic Scholar
xAtlas: Scalable small variant calling across heterogeneous next-generation sequencing experiments
J. Farek, D. Hughes, A. Mansfield, O. Krasheninina +9 more
2018bioRxiv42 citations Open access
Semantic Scholar
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk
Bing Yu, S. Pulit, Shih-Jen Hwang, J. Brody +31 more
2015Circulation: Cardiovascular Genetics42 citations Open access
Semantic Scholar
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
2016American Journal of Human Genetics41 citations Open access
Semantic Scholar
Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals
H. Doddapaneni, S. Cregeen, R. Sucgang, Q. Meng +17 more
2020bioRxiv40 citations Open access
Semantic Scholar
Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes
G. Hindy, Peter Dornbos, M. Chaffin, Da-Jiang J. Liu +179 more
2020bioRxiv38 citations Open access
Semantic Scholar
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants
Xu-Tong Zhao, D. Qiao, Chao-Jie Yang, S. Kasela +65 more
2020Nature Communications32 citations Open access
Semantic Scholar
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study
P. D. de Vries, Bing Yu, E. Feofanova, Ginger A. Metcalf +7 more
2017Human Molecular Genetics32 citations Open access
Semantic Scholar
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
2016American Journal of Human Genetics31 citations Open access
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
S. Choi, S. Jurgens, Ling Xiao, M. Hill +496 more
2025Nature Genetics29 citations Open access
Semantic Scholar
Structural variation across 138,134 samples in the TOPMed consortium
G. Jun, A. English, Ginger A. Metcalf, Jianzhi Yang +83 more
2023bioRxiv26 citations Open access
Semantic Scholar
Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications
David R. Murdock, E. Venner, D. Muzny, Ginger A. Metcalf +35 more
2021Genetics in Medicine25 citations Open access
Semantic Scholar
Whole genome sequence analysis of serum amino acid levels
Bing Yu, P. D. de Vries, Ginger A. Metcalf, Zhe Wang +7 more
2016Genome Biology24 citations Open access
Semantic Scholar
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
P. Natarajan, A. Pampana, Sarah E. Graham, S. Ruotsalainen +97 more
2021Nature Communications21 citations Open access
Semantic Scholar
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Xiao-Wei Hu, D. Qiao, Wonji Kim, M. Moll +47 more
2022American Journal of Human Genetics19 citations Open access
Semantic Scholar
Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk
S. Behera, Jonathan R. Belyeu, Xiao Chen, L. Paulin +22 more
2023bioRxiv18 citations Open access
Semantic Scholar
Fully resolved assembly of Cryptosporidium parvum
Vipin K. Menon, P. Okhuysen, C. Chappell, M. Mahmoud +17 more
2021bioRxiv16 citations Open access
Semantic Scholar
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
M. Wheeler, A. Stilp, Shu-Quan Rao, B. Halldórsson +55 more
2022Nature Communications15 citations Open access
Semantic Scholar
K-mer analysis of long-read alignment pileups for structural variant genotyping
A. English, Fabio Cunial, Ginger A. Metcalf, Richard A. Gibbs +1 more
2024bioRxiv14 citations Open access
Semantic Scholar
Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease.
Ya-Feng Pan, Xiao Sun, Xuenan Mi, Zhijie Huang +47 more
2022Human Molecular Genetics14 citations Open access
Semantic Scholar
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
L. Raffield, Apoorva K. Iyengar, Bi-Qi Wang, Sheila M. Gaynor +46 more
2019American Journal of Human Genetics13 citations Open access
Semantic Scholar
Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome
L. Polfus, E. Boerwinkle, R. Gibbs, Ginger A. Metcalf +10 more
2016Cold Spring Harbor molecular case studies13 citations Open access
Semantic Scholar
A pan-genome approach to decipher variants in the highly complex tandem repeat of LPA
Chen-Shan Chin, S. Behera, Ginger A. Metcalf, R. Gibbs +2 more
2022bioRxiv12 citations Open access
Semantic Scholar
Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study
E. Feofanova, Bing Yu, Ginger A. Metcalf, Xiao-Ming Liu +6 more
2018Genetics12 citations Open access
Semantic Scholar
Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation
J. Eicher, Ming-Huei Chen, A. Pitsillides, Hong-Huang Lin +13 more
2017Thrombosis and Haemostasis11 citations Open access
Semantic Scholar
muCNV: genotyping structural variants for population-level sequencing
G. Jun, F. Sedlazeck, Qi-Hui Zhu, A. English +5 more
2021Bioinform.9 citations Open access
Semantic Scholar
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xi-Hao Li, Han Chen, M. Selvaraj, Eric Van Buren +438 more
2025Nature Computational Science8 citations Open access
Semantic Scholar
Inter and intra-host diversity of RSV in hematopoietic stem cell transplant adults with normal and delayed viral clearance
V. Avadhanula, D. Agustinho, Vipin K. Menon, R. Chemaly +11 more
2023Virus Evolution8 citations Open access
Semantic Scholar
Whole Genome Analysis of Venous Thromboembolism: The Trans-Omics for Precision Medicine (TOPMed) Program
Amanda A. Seyerle, C. Laurie, B. Coombes, D. Jain +30 more
2023Circulation Genomic and Precision Medicine8 citations Open access
Semantic Scholar
Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016))
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
20167 citations Open access
Semantic Scholar
High-Quality Draft Genome Sequence of Francisella tularensis subsp. holarctica Strain OR96-0246
L. M. Atkins, M. Holder, N. Ajami, Ginger A. Metcalf +7 more
2015Genome Announcements7 citations Open access
Semantic Scholar
Author Correction: High-depth African genomes inform human migration and health
A. Choudhury, S. Aron, Laura R. Botigué, Dhriti Sengupta +28 more
2021Nature6 citations Open access
Semantic Scholar
Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
N. Pankratz, P. Wei, J. Brody, Ming-Huei Chen +27 more
2022Human Molecular Genetics5 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

D. Muzny×38
Invite
D. Muzny — researcher profile on SciRah
R. Gibbs×36
Invite
R. Gibbs — researcher profile on SciRah
E. Boerwinkle×27
Invite
E. Boerwinkle — researcher profile on SciRah
A. Morrison×18
Invite
A. Morrison — researcher profile on SciRah

×17

Invite

J. Brody — researcher profile on SciRah

H. Doddapaneni×16

Invite

H. Doddapaneni — researcher profile on SciRah

Invite

A. Reiner — researcher profile on SciRah

Invite

L. Yanek — researcher profile on SciRah

Invite

B. Psaty — researcher profile on SciRah

F. Sedlazeck×13

Invite

F. Sedlazeck — researcher profile on SciRah

Invite

L. Cupples — researcher profile on SciRah

Invite

J. Rotter — researcher profile on SciRah