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David Bick

11PUBLICATIONS
57CO-AUTHORS
Medical infection agents (incl. prions)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Human information interaction and retrievalInformation systems development methodologies and practice
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Journal

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

|Dec 27, 2023
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders.

Shamima Rahman, David Bick, Richard H Scott

|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

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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

Frequent Collaborators

3 joint publications

Vaidehi Jobanputra

3 joint publications

Stacie L Taylor

2 joint publications

David Dimmock

2 joint publications

Megan E Grove

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