Allan C. Wilson (1934–91): In memoriam Mary-Claire King

Por King, Mary-Claire
Publicado em 1992

2012 Presidential Address: The Scientist as a Citizen of the World

Por King, Mary-Claire
Publicado em 2013

Abundant novel transcriptional units and unconventional gene pairs on human chromosome 22

Por Lipovich, Leonard, King, Mary-Claire
Publicado em 2006

PCR detection of an MboI polymorphism in the ERBB2 (HER2; NEU) gene on chromosome 17q11.2-q12

Por Hall, Jeff M., King, Mary-Claire
Publicado em 1991

Response to DNA damage of CHEK2 missense mutations in familial breast cancer

Por Roeb, Wendy, Higgins, Jake, King, Mary-Claire
Publicado em 2012

SeqHelp: A Program to Analyze Molecular Sequences Utilizing Common Computational Resources

Por Lee, Ming K., Lynch, Eric D., King, Mary-Claire
Publicado em 1998

Accurate and exact CNV identification from targeted high-throughput sequence data

Por Nord, Alex S, Lee, Ming, King, Mary-Claire, Walsh, Tom
Publicado em 2011

A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31

Por Lipovich, Leonard, Lynch, Eric D, Lee, Ming K, King, Mary-Claire
Publicado em 2001

Genetics and Genomics: A Call for Papers

Por DeAngelis, Catherine D., Fontanarosa, Phil B., King, Mary-Claire, Pasche, Boris
Publicado em 2008

Genetics and Genomics: A Call for Papers

Por DeAngelis, Catherine D., Fontanarosa, Phil B., King, Mary-Claire, Pasche, Boris
Publicado em 2007

Response from Newman, et al

Por Newmann, Beth, Quesenberry, Charles P., King, Mary-Claire, Selby, Joseph V., Friedman, Gary D.
Publicado em 1991

Genomic structure of chromosome 17 deletions in BRCA1 associated ovarian cancers

Por Chisholm, Karen M., Goff, Barbara A., Garcia, Rochelle, King, Mary-Claire, Swisher, Elizabeth M.
Publicado em 2008

Comparative analysis of cancer genes in the human and chimpanzee genomes

Por Puente, Xose S, Velasco, Gloria, Gutiérrez-Fernández, Ana, Bertranpetit, Jaume, King, Mary-Claire, López-Otín, Carlos
Publicado em 2006

A truncating mutation in GPSM2 is associated with recessive nonsyndromic hearing loss

Por Yariz, Kemal O., Walsh, Tom, Akay, Hatice, Duman, Duygu, Akkaynak, Adil Cinar, King, Mary-Claire, Tekin, Mustafa
Publicado em 2011

Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene

Por Renbaum, Paul, Kellerman, Efrat, Jaron, Ranit, Geiger, Dan, Segel, Reeval, Lee, Ming, King, Mary Claire, Levy-Lahad, Ephrat
Publicado em 2009

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

Por Yariz, Kemal O., Walsh, Tom, Uzak, Asli, Spiliopoulos, Michail, Duman, Duygu, Onalan, Gogsen, King, Mary-Claire, Tekin, Mustafa
Publicado em 2011

A Genomewide Screen for Suppressors of Alu-Mediated Rearrangements Reveals a Role for PIF1

Por Chisholm, Karen M., Aubert, Sarah D., Freese, Krister P., Zakian, Virginia A., King, Mary-Claire, Welcsh, Piri L.
Publicado em 2012

FAM111B MUTATION IS ASSOCIATED WITH INHERITED EXOCRINE PANCREATIC DYSFUNCTION

Por Seo, Aaron, Walsh, Tom, Lee, Ming, Ho, Phoenix, Hsu, Evelyn Kanyu, Sidbury, Robert, King, Mary-Claire, Shimamura, Akiko
Publicado no Pancreas (2016)

The Future of Psychiatric Research: Genomes and Neural Circuits

Por Akil, Huda, Brenner, Sydney, Kandel, Eric, Kendler, Kenneth S., King, Mary-Claire, Scolnick, Edward, Watson, James D., Zoghbi, Huda Y.
Publicado em 2010

CONTRIBUTION TO FAMILIAL BREAST CANCER OF INHERITED MUTATIONS IN THE BRCA2-INTERACTING PROTEIN PALB2

Por Casadei, Silvia, Norquist, Barbara M., Walsh, Tom, Stray, Sunday, Mandell, Jessica B., Lee, Ming K., Stamatoyannopoulos, John A., King, Mary-Claire
Publicado em 2011