Robert D. Steiner

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications”.

Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100282

N/A

0.261DataRank · unranked

4 citations

Robert D. Steiner, Anne Slavotinek, Tiago Faial, Michael J. Bamshad, Jehannine Austin +4 more

Breastfeeding Infants with Phenylketonuria in the United States and Canada

UNC Libraries(2020)10.17615/y7tj-3c62

N/A

0DataRank · unranked

0 citations

Gail M. Houck, Sandra A. Banta-Wright, Kathleen A. Knafl, Robert D. Steiner, Nancy Press

Apolipoprotein E–low density lipoprotein receptor interaction affects spatial memory retention and brain ApoE levels in an isoform-dependent manner

UNC Libraries(2020)10.17615/a70t-pz17

N/A

0DataRank · unranked

0 citations

Lance A. Johnson, Jacob Raber, Andrea E. DeBarber, Patrick M. Sullivan, Louise S. Merkens +3 more

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors

Differentiation(2022)10.1016/j.diff.2022.09.002

N/A

0DataRank · unranked

18 citations

Annabelle Enriquez, Robert D. Steiner, Cathy Raggio, Megan Higgins, Di Milnes +7 more

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337

N/A

0DataRank · unranked

21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more

ClinGen’s Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Genetics in Medicine(2022)10.1016/j.gim.2022.02.019

N/A

0DataRank · unranked

13 citations

Charisma L. Jenkins, Joanna E. Bulkley, Marian J. Gilmore, Kristy Lee, Christine M. Pak +17 more

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis

Human Molecular Genetics(2023)10.1093/hmg/ddad117

N/A

0DataRank · unranked

22 citations

Elizabeth Wohler, Vida Erfani, Guozhuang Li, Alexya N. Aguilera, Alberto Santiago-Cornier +11 more

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100840

N/A

0DataRank · unranked

3 citations

Chansonette Badduke, Steven J. Schrodi, Vinod Scaria, Onur Emre Onat, Majid Alfadhel +5 more

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

Human Molecular Genetics(2020)10.1093/hmg/ddaa258

N/A

0DataRank · unranked

26 citations

Annabelle Enriquez, Duncan B. Sparrow, David T. Humphreys, Aideen McInerney‐Leo, Paul Leo +29 more

Implementing evidence-based assertions of clinical actionability in the context of secondary findings: Updates from the ClinGen Actionability Working Group

Genetics in Medicine(2024)10.1016/j.gim.2024.101164

N/A

0DataRank · unranked

4 citations

Marian J. Gilmore, Joanna E. Bulkley, Pranesh Chakraborty, Orit Dagan‐Rosenfeld, Ann Katherine M. Foreman +21 more