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

Roni Zemet

Baylor College of Medicine

ORCID: 0000-0002-7746-3594

Also affiliated with Baylor Genetics

Medicine

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 10 papers. Top paper: “Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset”.

Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset

Human Genomics(2021)10.1186/s40246-021-00369-6
N/A
0DataRank · unranked
33 citations

Tomasz Gambin, Roni Zemet, Chung Wah Wu, Katharina Schulze, Yaping Yang +5 more

Detection of Low-Level Parental Somatic Mosaicism for Clinically Relevant Snvs and Indels Identified in a Large Exome Sequencing Dataset

Research Square(2021)10.21203/rs.3.rs-1020672/v1
N/A
0DataRank · unranked
1 citations

Tomasz Gambin, Roni Zemet, Chung Wah Wu, Katharina Schulze, Yaping Yang +5 more

Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.31989
N/A
0DataRank · unranked
52 citations

Patricia Morgan, Bimal P. Chaudhari, Isabel Filges, Teresa N. Sparks, Pablo Lapunzina +31 more

Implication of chromosomal microarray analysis prior to in‐utero repair of fetal open neural tube defect

Ultrasound in Obstetrics and Gynecology(2023)10.1002/uog.26152
N/A
0DataRank · unranked
10 citations

Eyal Krispin, Rebecca Johnson, Natasha Kumar, Lauren Westerfield, Samantha Stover +12 more

SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia

Human Genetics(2023)10.1007/s00439-023-02550-4
N/A
0DataRank · unranked
2 citations

Haowei Du, Tomasz Gambin, James R. Lupski, Pengfei Liu, Paweł Stankiewicz +1 more

SNV/indel hypermutator phenotype in biallelic RAD51C variant - Fanconi anemia

Research Square(2023)10.21203/rs.3.rs-2628288/v1
N/A
0DataRank · unranked
0 citations

Haowei Du, Tomasz Gambin, Pengfei Liu, James R. Lupski, Paweł Stankiewicz +1 more

Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108513
N/A
0DataRank · unranked
13 citations

Kyle D. Hope, Andrew C. Edmondson, Rameen Shah, Maria Patino, Abigail Yesso +7 more

Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study

American Journal of Obstetrics and Gynecology(2024)10.1016/j.ajog.2024.06.025
N/A
0DataRank · unranked
9 citations

Mohamad Ali Maktabi, Alexandra Tinfow, Jessica L. Giordano, Thomas M. Heisler, Qi Yan +22 more

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic–ischemic encephalopathy: A retrospective analysis

Clinical Genetics(2024)10.1111/cge.14522
N/A
0DataRank · unranked
8 citations

Roni Zemet, Matthew A. Shanahan, Brian Burnett, Elizabeth Mizerik, Jill A. Rosenfeld +5 more

Impact of prenatal genomics on clinical genetics practice

Best Practice & Research Clinical Obstetrics & Gynaecology(2024)10.1016/j.bpobgyn.2024.102545
N/A
0DataRank · unranked
6 citations

Ignatia B. Van den Veyver, Roni Zemet