🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Mary M. Jenkins

National Center on Birth Defects and Developmental Disabilities

ORCID: 0000-0002-4399-1348
MedicineBiochemistry, Genetics and Molecular Biology

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 6%percentile
0.224Author DataRank

Indexed papers

3in 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 3 indexed papers 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 →

Top data-sharing exemplar

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

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082
Top 62%
0.224DataRank
Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Papers

Driven by 19 papers — median percentile 0. Top paper: “A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study”.

A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62759
N/A
0.417DataRank · unranked
9 citations

Mario A. Cleves, Gary M. Shaw, Wendy N. Nembhard, Eirini Nestoridi, Mary M. Jenkins +11 more

Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63185
N/A
0.292DataRank · unranked
6 citations

Aniko Sabo, Lynn M. Almli, Mary M. Jenkins, Wendy N. Nembhard, A. J. Agopian +28 more

Real-world data are not always big data: the case for primary data collection on medication use in pregnancy in the context of birth defects research

American Journal of Epidemiology(2024)10.1093/aje/kwae060
N/A
0.269DataRank · unranked
5 citations

Martha M. Werler, Meredith M. Howley, Mary M. Jenkins, Jennita Reefhuis, Elizabeth C. Ailes

Exome sequencing identifies variants in infants with sacral agenesis

Birth Defects Research(2022)10.1002/bdr2.1987
N/A
0.241DataRank · unranked
4 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +21 more

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082
Top 62%
0.224DataRank
Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split‐Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study

Birth Defects Research(2025)10.1002/bdr2.2472
N/A
0.104DataRank · unranked
1 citations

Denise M. Kay, Faith Pangilinan, Lynn M. Almli, Mary M. Jenkins, Elizabeth Blue +24 more

Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study

Birth Defects Research(2024)10.1002/bdr2.2384
N/A
0DataRank · unranked
2 citations

Kristin J. Moore, K.E. North, Tania A. Desrosiers, Suzan L. Carmichael, Janson J. White +19 more

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia

UNC Libraries(2024)10.17615/94re-8d47
N/A
0DataRank · unranked
0 citations

Wendy N. Nembhard, Paul A. Romitti, Marcia L. Feldkamp, Y.J. Wang, Andrew F. Olshan +22 more

Exome sequencing identifies variants in infants with sacral agenesis

UNC Libraries(2024)10.17615/sevc-bn40
N/A
0DataRank · unranked
0 citations

Faith Pangilinan, Andrew F. Olshan, Richard H. Finnell, Martha M. Werler, Cynthia A. Moore +24 more

A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

UNC Libraries(2024)10.17615/ph8v-yc50
N/A
0DataRank · unranked
0 citations

Mary M. Jenkins, Sara R. Rashkin, Paul A. Romitti, Andrew F. Olshan, Marilyn L. Browne +11 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

UNC Libraries(2024)10.17615/4645-7p40
N/A
0DataRank · unranked
0 citations

Marcia L. Feldkamp, Nathan Pankratz, Lawrence C. Brody, John W. Lane, K.M. Conway +18 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

UNC Libraries(2024)10.17615/4h14-yj71
N/A
0DataRank · unranked
0 citations

Jianlin Li, Paul A. Romitti, Wendy N. Nembhard, Andrew F. Olshan, Marilyn L. Browne +11 more

Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data

UNC Libraries(2024)10.17615/j34v-vj41
Top 100%
0DataRank
Top 100%0 citations

Wendy N. Nembhard, Shiran Shapira, Andrew F. Olshan, Elizabeth Blue, Nanette M. Nascone‐Yoder +27 more

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101851
N/A
0DataRank · unranked
4 citations

Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai +72 more

Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62439
N/A
0DataRank · unranked
8 citations

Marcia L. Feldkamp, Nathan Pankratz, John Lane, Denise M. Kay, Kristin M. Conway +17 more

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

PLoS Genetics(2021)10.1371/journal.pgen.1009413
N/A
0DataRank · unranked
4 citations

Emine Bircan, Xinyu Tang, Mohammed S. Orloff, Charlotte A. Hobbs, Marilyn L. Browne +11 more

Exome sequencing identifies genetic variants in anophthalmia and microphthalmia

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62874
N/A
0DataRank · unranked
8 citations

Wei Yang, Yuejun Wang, Chen Ma, Cynthia J. Curry, Daniel McGoldrick +21 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

The national birth defects prevention study: A review of the methods: NBDPS METHODS REVIEW

UNC Libraries(2020)10.17615/w46z-wa53
Top 100%
0DataRank
Top 100%0 citations

Marilyn L. Browne, Marcia L. Feldkamp, Suzanne M. Gilboa, Gary M. Shaw, Charlotte A. Hobbs +10 more