Peter White

Also affiliated with University of Leicester, The Ohio State University

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 14 papers. Top paper: “Continuous Microevolution Accelerates Disease Progression during Sequential Episodes of Infection”.

Continuous Microevolution Accelerates Disease Progression during Sequential Episodes of Infection

Cell Reports(2020)10.1016/j.celrep.2020.02.019

N/A

0DataRank · unranked

14 citations

Rachael L. Hardison, Audra R. Fullen, Rachel M. Wallace, David Gordon, Peter White +4 more

Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population

GigaScience(2021)10.1093/gigascience/giab023

N/A

0DataRank · unranked

33 citations

Grant Lammi, James Li, David Gordon, Harkness Kuck, Benjamin Kelly +3 more

L-Arabinose Transport and Metabolism in Salmonella Influences Biofilm Formation

Frontiers in Cellular and Infection Microbiology(2021)10.3389/fcimb.2021.698146

N/A

0DataRank · unranked

23 citations

Lindsey O’Neal, Matthew R. Parsek, James Fitch, Peter White, John S. Gunn +1 more

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100037

N/A

0DataRank · unranked

15 citations

Wenjuan Zhu, George C. Gabriel, Cullen B. Young, Kylia Williams, Lisa J. Martin +36 more

Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma

Acta Neuropathologica Communications(2021)10.1186/s40478-021-01164-z

N/A

0DataRank · unranked

14 citations

Alexander Feldman, Esko A. Kautto, Sean McGrath, Anthony R. Miller, Maria Elena Hernandez‐Gonzalez +26 more

Use of machine learning to classify high-risk variants of uncertain significance in lamin A/C cardiac disease

Heart Rhythm(2021)10.1016/j.hrthm.2021.12.019

N/A

0DataRank · unranked

9 citations

David Gordon, Uddalak Majumdar, Patrick J. Lawrence, Adrianna Matos-Nieves, Katherine Myers +6 more

A Multi-Omics Approach Using a Mouse Model of Cardiac Malformations for Prioritization of Human Congenital Heart Disease Contributing Genes

Frontiers in Cardiovascular Medicine(2021)10.3389/fcvm.2021.683074

N/A

0DataRank · unranked

8 citations

Sathiyanarayanan Manivannan, Uddalak Majumdar, Kim L. McBride, Peter White, Vidu Garg +1 more

Psychological stress disrupts intestinal epithelial cell function and mucosal integrity through microbe and host-directed processes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.25.465765

N/A

0DataRank · unranked

0 citations

Amy R. Mackos, Robert M. Jaggers, Patricia C. Brewster, Mikaela Webb, Chia‐Hao Lin +6 more

Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery

PLoS Genetics(2022)10.1371/journal.pgen.1010236

N/A

0DataRank · unranked

22 citations

David Cunningham, Gloria Zender, Patrick J. Lawrence, Jacqueline S. Penaloza, Hui Lin +13 more

CRISPR-Cas9 homology-independent targeted integration of exons 1–19 restores full-length dystrophin in mice

Molecular Therapy — Methods & Clinical Development(2023)10.1016/j.omtm.2023.08.009

N/A

0DataRank · unranked

19 citations

Stefan Nicolau, Tatyana A. Vetter, G. Dufresne, E. Frair, J. Sarff +5 more

Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis

Pediatric Research(2023)10.1038/s41390-023-02811-y

N/A

0DataRank · unranked

16 citations

Sathiyanarayanan Manivannan, Uddalak Majumdar, David Gordon, Patrick J. Lawrence, Mona Aljuhani +9 more

Glucocorticoid- and pioglitazone-induced proteinuria reduction in experimental NS both correlate with glomerular ECM modulation

iScience(2023)10.1016/j.isci.2023.108631

N/A

0DataRank · unranked

4 citations

Julie Dougherty, Yu Kamigaki, Shipra Agrawal, Saranga Wijeratne, James Fitch +6 more

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100232

N/A

0DataRank · unranked

2 citations

Janson J. White, Michael Dush, William W. Gordon, Brent Wyatt, Peter White +22 more

CNVoyant a machine learning framework for accurate and explainable copy number variant classification

Scientific Reports(2024)10.1038/s41598-024-72470-4

N/A

0DataRank · unranked

7 citations

Defne Ceyhan, Austin Antoniou, Bimal P. Chaudhari, Peter White, Robert Schuetz