Hannah Wand

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines”.

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8

N/A

2.6DataRank · unranked

85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Combining clinical and polygenic risk improves stroke prediction among individuals with atrial fibrillation

medRxiv(2020)10.1101/2020.06.17.20134163

N/A

0DataRank · unranked

14 citations

Anna Shcherbina, Johanne Marie Justesen, Mintu P. Turakhia, Marco Pérez, Hannah Wand +6 more

The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

Genetics in Medicine(2021)10.1016/j.gim.2021.09.012

N/A

0DataRank · unranked

168 citations

Michael A. Iacocca, Lukáš Tichý, Hannah Wand, C. Lisa Kurtz, Heather Zimmermann +23 more

Application of a framework to guide genetic testing communication across clinical indications

Genome Medicine(2021)10.1186/s13073-021-00887-x

N/A

0DataRank · unranked

30 citations

Eric P. Tricou, Kelly E. Ormond, Juliann M. Savatt, Curtis R. Coughlin, W. Andrew Faucett +11 more

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663

N/A

0DataRank · unranked

5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

medRxiv(2021)10.1101/2021.03.17.21252755

N/A

0DataRank · unranked

3 citations

Michael A. Iacocca, Lukáš Tichý, Hannah Wand, C. Lisa Kurtz, Heather Zimmermann +23 more

Including multiracial individuals is crucial for race, ethnicity and ancestry frameworks in genetics and genomics

Nature Genetics(2023)10.1038/s41588-023-01394-y

N/A

0DataRank · unranked

35 citations

Hannah Wand, Jennifer L. Young, Genevieve L. Wojcik, Daphne Oluwaseun Martschenko

Improving reporting standards for polygenic scores in risk prediction studies

medRxiv(2020)10.1101/2020.04.23.20077099

N/A

0DataRank · unranked

55 citations

Samuel A. Lambert, Cecelia P. Tamburro, Michael A. Iacocca, Jack W. O’Sullivan, Catherine H. Sillari +28 more

Re-envisioning community genetics: community empowerment in preventive genomics

Journal of Community Genetics(2023)10.1007/s12687-023-00638-y

N/A

0DataRank · unranked

8 citations

Daphne Oluwaseun Martschenko, Annamaria Smitherman, Sheryl Michelson, Ting Pun, John S. Witte +9 more