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

Alexander Katz

University of Michigan

ORCID: 0000-0001-9706-9490

Also affiliated with Michigan United

DentistryBiochemistry, 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 10 papers. Top paper: “Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture”.

Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.121.003496

N/A

0.806DataRank · unranked

22 citations

Min‐Lee Yang, Michael G. Levin, Catherine Tcheandjieu, Michael R. Mathis, Kristina L. Hunker +86 more

Management of Secondary Genomic Findings

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.002

N/A

0DataRank · unranked

60 citations

Robert L. Nussbaum, Benjamin D. Solomon, Heidi L. Rehm, Marc S. Williams, Leslie G. Biesecker +1 more

Pitfalls and challenges in genetic test interpretation: An exploration of genetic professionals experience with interpretation of results

Clinical Genetics(2021)10.1111/cge.13917

N/A

0DataRank · unranked

56 citations

Catherine Gooch, Alexander Katz, Jessica Wakelee, Anne Slavotinek, Bruce R. Korf +1 more

The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort

Genetics in Medicine(2021)10.1016/j.gim.2021.11.012

N/A

0DataRank · unranked

17 citations

Marie‐Luise Brennan, Bailey Radenbaugh, Seeley Yoo, Sophia M. Hernandez, Katie L. Lewis +4 more

Genotype first: Clinical genomics research through a reverse phenotyping approach

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2022.12.004

N/A

0DataRank · unranked

73 citations

Justice Obasohan, Justin Paschall, Suiyuan Zhang, Sumeeta Singh, George L. Maxwell +6 more

Advancements in the Genetics of Spontaneous Coronary Artery Dissection

Current Cardiology Reports(2023)10.1007/s11886-023-01989-1

N/A

0DataRank · unranked

8 citations

Santhi K. Ganesh, Alexander Katz

ATP1A1-linked diseases require a malfunctioning protein product from one allele

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research(2023)10.1016/j.bbamcr.2023.119572

N/A

0DataRank · unranked

4 citations

Victoria C. Young, Ryan Sweazey, Alexandria Padro, Jeannie K. Lee, Tulio Bueso +12 more

ATP1A1 -linked diseases require a malfunctioning protein product from one allele

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.05.531165

N/A

0DataRank · unranked

0 citations

Victoria C. Young, Ryan Sweazey, Alexandria Padro, Jeannie K. Lee, Tulio Bueso +12 more

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

Nature Communications(2020)10.1038/s41467-020-17558-x

N/A

0DataRank · unranked

102 citations

Min‐Lee Yang, Mark Trinder, Catherine Tcheandjieu, Chang Xu, Andrew Starovoytov +22 more

From Atherosclerosis to Spontaneous Coronary Artery Dissection: Defining a Clinical and Genetic Risk Spectrum for Myocardial Infarction

Current Atherosclerosis Reports(2024)10.1007/s11883-024-01208-4

N/A

0DataRank · unranked

10 citations

Trisha Gupte, Santhi K. Ganesh, Alexander Katz