Christopher W Whelan
6PUBLICATIONS
38CO-AUTHORS
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Publications (6)
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|Jan 02, 2025
Rare germline structural variants increase risk for pediatric solid tumors.Riaz Gillani, Ryan L Collins, Jett Crowdis
|Feb 04, 2021
Author Correction: A structural variation reference for medical and population genetics.Ryan L Collins, Harrison Brand, Konrad J Karczewski
|Dec 23, 2020
Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice.Melis Yilmaz, Esra Yalcin, Jessy Presumey
|Jun 06, 2020
Complement genes contribute sex-biased vulnerability in diverse disorders.Nolan Kamitaki, Aswin Sekar, Robert E Handsaker
|May 29, 2020
A structural variation reference for medical and population genetics.Ryan L Collins, Harrison Brand, Konrad J Karczewski
|May 18, 2018
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.Karol Estrada, Christopher W Whelan, Fengmei Zhao
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Frequent Collaborators
3 joint publications
Michael E Talkowski
3 joint publications
Ryan L Collins
2 joint publications
Robert E Handsaker
2 joint publications
Konrad J Karczewski
2 joint publications
Xuefang Zhao
2 joint publications
Jessica Alföldi
2 joint publications
Laurent C Francioli
2 joint publications
Anne O'Donnell-Luria
2 joint publications
Elise Valkanas
2 joint publications
Kent D Taylor
