Author

Amanda Stillwell

Baylor College of Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Emily YoungiD· 2 shared Isabel Alfradique‐DunhamiD· 2 shared Joseph J. JankoviciD· 2 shared Joshua M ShulmaniD· 2 shared Andrew SingletoniD· 1 shared Anita KawiD· 1 shared Anusha Tejomurtula· 1 shared Bo YuaniD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Emily YoungORCID

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2 papers

Recent·Most cited

Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes

Isabel Alfradique‐Dunham, Rami Al‐Ouran, Rainer von Coelln, Cornelis Blauwendraat, Emily J. Hill, Lan Luo, Amanda Stillwell, Emily Young, Anita Kaw, Manuela M. X. Tan, Calwing Liao, Dena G. Hernandez, Lasse Pihlstrøm, Donald G. Grosset, Lisa M. Shulman, , Joshua M Shulman

This study identifies genetic associations with Parkinson disease motor subtypes using GWAS, finding novel variants and suggesting overlap with essential tremor genetics.

Neurology Genetics · Apr 1, 2021Peer-reviewedGenomics

Integrated Sequencing & Array Comparative Genomic Hybridization in Familial Parkinson’s Disease

Laurie A. Robak, Renqian Du, Bo Yuan, Shen Gu, Isabel Alfradique‐Dunham, Vismaya Kondapalli, Evelyn Hinojosa, Amanda Stillwell, Emily Young, Chaofan Zhang, Xiaofei Song, Haowei Du, Tomasz Gambin, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, , Joshua M Shulman

The paper combines exome sequencing and array-based comparative genomic hybridization to identify genetic risk factors in familial Parkinson’s disease, finding novel SNVs and CNVs.

bioRxiv · Nov 11, 2019 · PreprintGenetics