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Author/Creator Bick, David

1. A study of elective genome sequencing and pharmacogenetic testing in an unselected population. Issue 9 (27th July 2021)

Authors:
Cochran, Meagan; East, Kelly; Greve, Veronica; Kelly, Melissa; Kelley, Whitley; Moore, Troy; Myers, Richard M.; Odom, Katherine; Schroeder, Molly C.; Bick, David
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 9(2021)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Issue 2 (9th April 2019)

Authors:
Zastrow, Diane B.; Kohler, Jennefer N.; Bonner, Devon; Reuter, Chloe M.; Fernandez, Liliana; Grove, Megan E.; Fisk, Dianna G.; Yang, Yaping; Eng, Christine M.; Ward, Patricia A.; Bick, David; Worthey, Elizabeth A.; Fisher, Paul G.; Ashley, Euan A.; Bernstein, Jonathan A.; Wheeler, Matthew T.
Other Names:
Merker Jason investigator.; Schelley Susan investigator.; Enns Gregory investigator.; Montgomery Stephen investigator.; Zappala Zach investigator.; Fresard Laure investigator.; Prybol Cameron investigator.; Taylor Robert investigator.; McFarland Robert investigator.; Holmes Matthew investigator.;...
Journal:
Journal of genetic counseling
Issue:
Volume 28:Issue 2(2019)
Page Start:
213
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Elective genomic testing: Practice resource of the National Society of Genetic Counselors. Issue 2 (4th January 2023)

Authors:
Blout Zawatsky, Carrie L.; Bick, David; Bier, Louise; Funke, Birgit; Lebo, Matthew; Lewis, Katie L.; Orlova, Ekaterina; Qian, Emily; Ryan, Lauren; Schwartz, Marci L. B.; Soper, Emily R.
Journal:
Journal of genetic counseling
Issue:
Volume 32:Issue 2(2023)
Page Start:
281
Record Type:
Journal Article
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9. Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. (2nd May 2018)

Authors:
Liu, Ning; Schoch, Kelly; Luo, Xi; Pena, Loren D M; Bhavana, Venkata Hemanjani; Kukolich, Mary K; Stringer, Sarah; Powis, Zöe; Radtke, Kelly; Mroske, Cameron; Deak, Kristen L; McDonald, Marie T; McConkie-Rosell, Allyn; Markert, M Louise; Kranz, Peter G; Stong, Nicholas; Need, Anna C; Bick, David;...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 14(2018:Jul. 15)
Page Start:
2454
Record Type:
Journal Article
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10. High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation. Issue 11 (21st August 2015)

Authors:
Rojnueangnit, Kitiwan; Xie, Jing; Gomes, Alicia; Sharp, Angela; Callens, Tom; Chen, Yunjia; Liu, Ying; Cochran, Meagan; Abbott, Mary‐Alice; Atkin, Joan; Babovic‐Vuksanovic, Dusica; Barnett, Christopher P.; Crenshaw, Melissa; Bartholomew, Dennis W.; Basel, Lina; Bellus, Gary; Ben‐Shachar, Shay; Bi...
Journal:
Human mutation
Issue:
Volume 36:Issue 11(2015:Nov.)
Page Start:
1052
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗