Publications by authors named "Pamela L Brock"

5Publications

Characterizing the function of EPB41L4A in the predisposition to papillary thyroid carcinoma.

Authors:
Daniel F Comiskey Huiling He Sandya Liyanarachchi Mehek S Sheikh Isabella V Hendrickson Lianbo Yu Pamela L Brock Albert de la Chapelle

Sci Rep 2020 11 17;10(1):19984. Epub 2020 Nov 17.

Human Cancer Genetics Program and Department of Cancer Biology and Genetics, Comprehensive Cancer Center, College of Medicine, The Ohio State University Wexner Medical Center, 804 Biomedical Research Tower, 460 W 12th Ave., Columbus, OH, 43210, USA.

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November 2020

Variants in reveal distinct mechanisms for predisposition to papillary thyroid carcinoma.

Authors:
Daniel Forrest Comiskey Huiling He Sandya Liyanarachchi Mehek S Sheikh Luke K Genutis Isabella V Hendrickson Lianbo Yu Pamela L Brock Albert de la Chapelle

J Med Genet 2020 08 12;57(8):519-527. Epub 2020 Feb 12.

Cancer Biology and Genetics, Ohio State University Wexner Medical Center, Columbus, Ohio, USA

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August 2020

Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.

Authors:
Luke K Genutis Jerneja Tomsic Ralf A Bundschuh Pamela L Brock Michelle D Williams Sameek Roychowdhury Julie W Reeser Wendy L Frankel Mohammed Alsomali Mark J Routbort Russell R Broaddus Paul E Wakely John E Phay Christopher J Walker Albert de la Chapelle

Thyroid 2019 04 27;29(4):523-529. Epub 2019 Mar 27.

1 Department of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.

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April 2019

Neurotransmitter abnormalities and response to supplementation in SPG11.

Authors:
Adeline Vanderver Davide Tonduti Sarah Auerbach Johanna L Schmidt Sumit Parikh Gordon C Gowans Kelly E Jackson Pamela L Brock Marc Patterson Michelle Nehrebecky Rena Godfrey Wadih M Zein William Gahl Camilo Toro

Mol Genet Metab 2012 Sep 1;107(1-2):229-33. Epub 2012 Jun 1.

Department of Neurology, Children's National Medical Center, Washington, DC 20010-2970, USA.

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September 2012

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

Authors:
Blake C Ballif Sara A Hornor Elizabeth Jenkins Suneeta Madan-Khetarpal Urvashi Surti Kelly E Jackson Alexander Asamoah Pamela L Brock Gordon C Gowans Robert L Conway John M Graham Livija Medne Elaine H Zackai Tamim H Shaikh Joel Geoghegan Rebecca R Selzer Peggy S Eis Bassem A Bejjani Lisa G Shaffer

Nat Genet 2007 Sep 19;39(9):1071-3. Epub 2007 Aug 19.

Signature Genomic Laboratories, Spokane, Washington 99202, USA.

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September 2007