David Bick

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 22

Top Topics

Top Venues

Journal of inherited metabolic disease

NPJ genomic medicine

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics 143 (3) (2024)
Daniel Brooks, Elizabeth Burke, Sukyeong Lee, Tanya N Eble, Melanie O'Leary, Ikeoluwa A Osei-Owusu, Michael J Bamshad, Shweta U Dhar, Lisa Emrick, David Bick, Michelle Nehrebecky, Ellen Macnamara, Dídac Casas-Alba, Judith Armstrong, Carolina Prat, Antonio Federico Martínez-Monseny, Francesc Palau, Pengfei Liu, David Adams, null null, Seema Lalani, Jill Anne Rosenfeld, Lindsay C Burrage
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Human genetics (2024)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease 47 (1) (2023)
Shamima Rahman, David Bick, Richard H Scott
Whole genome sequencing to screen 100 000 newborns for treatable genetic disorders. Journal of inherited metabolic disease (2023)
Robin Z Hayeems, Stephanie Luca, Anna C E Hurst, Meagan Cochran, Chelsea Owens, Alomgir Hossain, Lauren Chad, M Stephen Meyn, Eleanor Pullenayegum, Wendy J Ungar, David Bick
Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity. European journal of human genetics : EJHG 30 (12) (2022)
Christina A Austin-Tse, Vaidehi Jobanputra, Denise L Perry, David Bick, Ryan J Taft, Eric Venner, Richard A Gibbs, Edwin J Young, Sarah Barnett, John W Belmont, Nicole Boczek, Shimul Chowdhury, Katarzyna A Ellsworth, Saurav Guha, Shashikant Kulkarni, Cherisse Marcou, Linyan Meng, David R Murdock, Atteeq U Rehman, Elizabeth Spiteri, Amanda Thomas-Wilson, Hutton M Kearney, Heidi L Rehm, null null
Best practices for the interpretation and reporting of clinical whole genome sequencing. NPJ genomic medicine 7 (1) (2022)
Meagan Cochran, Kelly East, Veronica Greve, Melissa Kelly, Whitley Kelley, Troy Moore, Richard M Myers, Katherine Odom, Molly C Schroeder, David Bick
A study of elective genome sequencing and pharmacogenetic testing in an unselected population. Molecular genetics & genomic medicine 9 (9) (2021)
David Bick, Sarah L Bick, David P Dimmock, Tom A Fowler, Mark J Caulfield, Richard H Scott
An online compendium of treatable genetic disorders. American journal of medical genetics. Part C, Seminars in medical genetics 187 (1) (2020)
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Matthew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey, Vaidehi Jobanputra, David P Dimmock, Hutton M Kearney, David Bick, Shashikant Kulkarni, Stacie L Taylor, John W Belmont, Dimitri J Stavropoulos, Niall J Lennon, null null
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. NPJ genomic medicine 5 (2020)
Robin Z Hayeems, David P Dimmock, David Bick, John W Belmont, Robert C Green, Brendan Lanpher, Vaidehi Jobanputra, Roberto Mendoza-Londono, Shashi Kulkarni, Megan E Grove, Stacie L Taylor, Euan Ashley, null null
Clinical utility of genomic sequencing: a measurement toolkit. NPJ genomic medicine 5 (1) (2020)
Diane B Zastrow, Jennefer N Carter, Devon E Bonner, Nicolette Chun, Liliana Fernandez, Megan E Grove, Dianna G Fisk, null null, Yaping Yang, Christine M Eng, Patricia A Ward, David Bick, Elizabeth A Worthey, Paul Graham Fisher, Euan A Ashley, Jonathan A Bernstein, Matthew T Wheeler
A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing. Journal of genetic counseling 28 (2) (2020)
David Bick, Marilyn Jones, Stacie L Taylor, Ryan J Taft, John Belmont
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. Journal of medical genetics 56 (12) (2019)
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin, Gregory M Cooper, Soma Das, Joshua L Deignan, Michael O Dorschner, James P Evans, Arezou A Ghazani, Katrina A B Goddard, Michele C Gornick, Kelly D F Hagman, Tina Hambuch, Madhuri Hegde, Lucia A Hindorff, Ingrid A Holm, Gail P Jarvik, Amy Knight Johnson, Lindsey Mighion, Massimo Morra, Sharon E Plon, Sumit Punj, Carolyn Sue Richards, Avni Santani, Brian H Shirts, Nancy B Spinner, Sha Tang, Karen E Weck, Susan M Wolf, Yaping Yang, Michael J Bamshad
A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)