David Bick
11PUBLICATIONS
57CO-AUTHORS
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Publications (11)
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|Mar 07, 2024
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.Daniel Brooks, Elizabeth Burke, Sukyeong Lee
|Oct 04, 2022
Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity.Robin Z Hayeems, Stephanie Luca, Anna C E Hurst
|Apr 09, 2022
Best practices for the interpretation and reporting of clinical whole genome sequencing.Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry
|Jul 27, 2021
A study of elective genome sequencing and pharmacogenetic testing in an unselected population.Meagan Cochran, Kelly East, Veronica Greve
|Dec 22, 2020
An online compendium of treatable genetic disorders.David Bick, Sarah L Bick, David P Dimmock
|Dec 15, 2020
Clinical utility of genomic sequencing: a measurement toolkit.Robin Z Hayeems, David Dimmock, David Bick
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Frequent Collaborators
3 joint publications
Vaidehi Jobanputra
3 joint publications
Stacie L Taylor
2 joint publications
David Dimmock
2 joint publications
Megan E Grove
2 joint publications
Heidi L Rehm
1 joint publications
Laura M Amendola
1 joint publications
Jonathan S Berg
1 joint publications
Laura K Conlin
1 joint publications
Joshua L Deignan
1 joint publications
Katrina A Goddard
