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论文共 384 篇作者统计合作学者相似作者

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Improved Allele Frequencies in Gnomad Through Local Ancestry Inference
Elizabeth G Atkinson, Pragati Kore, Michael Wilson,Grace Tiao, Katherine R Chao, Phil Darnowsky, Nick Watts, Jessica Honorato-Mauer, Samantha M. Baxter, Genome Aggregation Database Consortium,Heidi Rehm,Mark Daly, Konrad J. Karczewski
biorxiv（2024）
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Mitochondrial DNA Variant Detection in over 4000 Rare Disease Families by the Systematic Analysis of Exome, Genome, and RNA Sequencing Data
Sarah Stenton, Kristen M. Laricchia, Sushma Chaluvadi, Nicole J. Lake,Monkol Lek,Mark Fleming,Dean Campagna,Eric Pierce,Kinga Bujakowska,Emily Place,Heidi Rehm, Anne O'Donnell-Luria
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 20-21
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P138: Evaluating the Impact of Gnomad V4 on Genetic Prevalence Estimates*
Samantha Baxter,Moriel Singer-Berk,Kathryn Russell,Mutaz Amin, Carmen Glaze,Riley Grant, Josephine Lee, Nick Watts, Michael Wilson,Heidi Rehm,Anne O'Donnell-Luria
Genetics in Medicine Open (2024): 101035
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Exome Copy Number Variant (CNV) Detection, Analysis, and Curation from 6,678 Families with Undiagnosed Rare Genetic Disease
Gabrielle Lemire,Kathryn Russell,Samantha Baxter,Katherine Chao, Emily Evangelista, Moriel Singer-Berk, Alba Sanchis-Juan,Emily Groopman,Isaac Wong,Stephanie DiTroia,Eleina England,Julia Goodrich,Lynn Pais,Christina Austintse, Emily O'Heir,Hana Snow, Ikeoluwa A. Osei-Owusu,Jack Fu,Daniel MacArthur,Heidi Rehm,Michael Talkowski, Harrison Brand, Anne O'Donnell-Luria
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 45-45
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作者统计

#Papers: 386

#Citation: 51638

H-Index: 73

G-Index: 227

Sociability: 8

Diversity: 0

Activity: 6

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