Submissions from 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry., Louis Viollet, Gustavo Glusman, Kelley J Murphy, Tara M Newcomb, Sandra P Reyna, Matthew Sweney, Benjamin Nelson, Frederick Andermann, Eva Andermann, Gyula Acsadi, Richard L Barbano, Candida Brown, Mary E Brunkow, Harry T Chugani, Sarah R Cheyette, Abigail Collins, Suzanne D DeBrosse, David Galas, Jennifer Friedman, Leroy Hood, Chad Huff, Lynn B Jorde, Mary D King, Bernie LaSalle, Richard J Leventer, Aga J Lewelt, Mylynda B Massart, Mario R Mérida, Louis J Ptáček, Jared C Roach, Robert S Rust, Francis Renault, Terry D Sanger, Marcio A Sotero de Menezes, Rachel Tennyson, Peter Uldall, Yue Zhang, Mary Zupanc, Winnie Xin, Kenneth Silver, and Kathryn J Swoboda
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry., Louis Viollet, Gustavo Glusman, Kelley J Murphy, Tara M Newcomb, Sandra P Reyna, Matthew Sweney, Benjamin Nelson, Frederick Andermann, Eva Andermann, Gyula Acsadi, Richard L Barbano, Candida Brown, Mary E Brunkow, Harry T Chugani, Sarah R Cheyette, Abigail Collins, Suzanne D DeBrosse, David Galas, Jennifer Friedman, Leroy Hood, Chad Huff, Lynn B Jorde, Mary D King, Bernie LaSalle, Richard J Leventer, Aga J Lewelt, Mylynda B Massart, Mario R Mérida, Louis J Ptáček, Jared C Roach, Robert S Rust, Francis Renault, Terry D Sanger, Marcio A Sotero de Menezes, Rachel Tennyson, Peter Uldall, Yue Zhang, Mary Zupanc, Winnie Xin, Kenneth Silver, and Kathryn J Swoboda
Submissions from 2014
Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease., Matthew A Lalli, Hannah C Cox, Mary L Arcila, Liliana Cadavid, Sonia Moreno, Gloria Garcia, Lucia Madrigal, Eric M Reiman, Mauricio Arcos-Burgos, Gabriel Bedoya, Mary E Brunkow, Gustavo Glusman, Jared C Roach, Leroy Hood, Kenneth S Kosik, and Francisco Lopera
Submissions from 2013
Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis., Martyn K Robinson, John Caminis, and Mary E Brunkow
Submissions from 2012
Disruption of Fnip1 reveals a metabolic checkpoint controlling B lymphocyte development., Heon Park, Karen Staehling, Mark Tsang, Mark W Appleby, Mary E Brunkow, Daciana Margineantu, David M Hockenbery, Tania Habib, H Denny Liggitt, George Carlson, and Brian M Iritani
