Kim L. McBride

Also affiliated with Alberta Children's Hospital, The University of Texas Health Science Center at Houston

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 2%percentile

2.0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Lessons learned from 40 novel PIGA patients and a review of the literature

Epilepsia(2020)10.1111/epi.16545

Top 10%

2.0DataRank

Top 10%58 citations

Alexej Knaus, Manuela Pendziwiat, Alexandra Afenjar, Tahsin Stefan Barakat, Friedrich Bosch +49 more

Papers

Driven by 18 papers — median percentile 90. Top paper: “Lessons learned from 40 novel PIGA patients and a review of the literature”.

Lessons learned from 40 novel PIGA patients and a review of the literature

Epilepsia(2020)10.1111/epi.16545

Top 10%

2.0DataRank

Top 10%58 citations

Alexej Knaus, Manuela Pendziwiat, Alexandra Afenjar, Tahsin Stefan Barakat, Friedrich Bosch +49 more

Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve

Heart(2024)10.1136/heartjnl-2024-324669

N/A

0.251DataRank · unranked

4 citations

Sara Mansoorshahi, Steven Grant Carlisle, Catherina Tovar Pensa, Abi Watts, Courtney McNeely +19 more

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0

N/A

0DataRank · unranked

60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs)

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.630069

N/A

0DataRank · unranked

33 citations

Kim L. McBride, Vidu Garg, Mingtao Zhao, Hui Lin

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

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

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

Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)

Stem Cell Research(2022)10.1016/j.scr.2022.102893

N/A

0DataRank · unranked

3 citations

Matthew Alonzo, Shiqiao Ye, Hui Lin, Lumariz Hernandez-Rosario, Kim L. McBride +4 more

Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS)

Stem Cell Research(2022)10.1016/j.scr.2022.102892

N/A

0DataRank · unranked

2 citations

Javier Contreras, Shiqiao Ye, Hui Lin, Lumariz Hernandez-Rosario, Kim L. McBride +4 more

Generation and characterization of a human induced pluripotent stem cell (iPSC) line from a patient with congenital heart disease (CHD)

Stem Cell Research(2022)10.1016/j.scr.2022.102958

N/A

0DataRank · unranked

2 citations

Shiqiao Ye, Zhaohui Xu, Jacqueline S. Penaloza, Mona Aljuhani, Tatyana A. Vetter +3 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

A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100814

N/A

0DataRank · unranked

15 citations

Lindsey R. Helvaty, Ming Li, William L. Border, Sara Fitzgerald‐Butt, Vidu Garg +11 more

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

European Journal of Human Genetics(2023)10.1038/s41431-023-01451-4

N/A

0DataRank · unranked

8 citations

Xiaonan Zhao, Nichole Owen, Pamela N. Luna, Ida Vogel, Inger Lily Hjuler Dorf +27 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

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies

npj Genomic Medicine(2024)10.1038/s41525-024-00398-9

N/A

0DataRank · unranked

3 citations

Jeshurun C. Kalanithy, Gabriel C. Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M. Lopes +66 more

Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes

Hearts(2024)10.3390/hearts5030018

N/A

0DataRank · unranked

0 citations

Colin R. Ward, Megan L. Svetgoff, Héctor I. Michelena, Anna Sabaté-Rotés, Julie De Backer +17 more

Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans

UNC Libraries(2020)10.17615/09fe-9a09

N/A

0DataRank · unranked

24 citations

Jennifer M. Grossman, Yaoling Shu, Lee A. Hebert, Kim L. McBride, Yee Ling Wu +18 more

Kim L. McBride

Indexed papers

Top data-sharing exemplar

Papers