Sheldon-Hall syndrome

Por Bamshad Michael J, Toydemir Reha M
Publicado em 2009-03-01

Sheldon-Hall syndrome

Por Toydemir, Reha M, Bamshad, Michael J
Publicado em 2009

Massively parallel sequencing and rare disease

Por Ng, Sarah B., Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay
Publicado em 2010

Characteristics of Neutral and Deleterious Protein-Coding Variation among Individuals and Populations

Por Fu, Wenqing, Gittelman, Rachel M., Bamshad, Michael J., Akey, Joshua M.
Publicado em 2014

Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways

Por Freeze, Hudson H., Chong, Jessica X., Bamshad, Michael J., Ng, Bobby G.
Publicado em 2014

Self-guided management of exome and whole genome sequencing results: changing the results return model

Por Yu, Joon-Ho, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Publicado em 2013

Genomics Really Gets Personal: How Exome and Whole Genome Sequencing Challenge the Ethical Framework of Human Genetics Research

Por Tabor, Holly K., Berkman, Benjamin E., Hull, Sara Chandros, Bamshad, Michael J.
Publicado no Am J Med Genet A (2011)

The promise and limitations of population exomics for human evolution studies

Por Tennessen, Jacob A, O'Connor, Timothy D, Bamshad, Michael J, Akey, Joshua M
Publicado em 2011

Presence of epilepsy-associated variants in large exome databases

Por Cherepanova, Natalya S., Leslie, Elizabeth, Ferguson, Polly J., Bamshad, Michael J., Bassuk, Alexander G.
Publicado em 2013

Attitudes of African Americans toward Return of Results from Exome and Whole Genome Sequencing

Por Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Publicado em 2013

Estimates of Continental Ancestry Vary Widely among Individuals with the Same mtDNA Haplogroup

Por Emery, Leslie S., Magnaye, Kevin M., Bigham, Abigail W., Akey, Joshua M., Bamshad, Michael J.
Publicado no Am J Hum Genet (2015)

Attitudes of Non-African American Focus Group Participants Toward Return of Results from Exome and Whole Genome Sequencing

Por Yu, Joon-Ho, Crouch, Julia, Jamal, Seema M., Bamshad, Michael J., Tabor, Holly K.
Publicado no Am J Med Genet A (2014)

Natural Selection and Molecular Evolution in PTC, a Bitter-Taste Receptor Gene

Por Wooding, Stephen, Kim, Un-kyung, Bamshad, Michael J., Larsen, Jennifer, Jorde, Lynn B., Drayna, Dennis
Publicado em 2004

Attitudes of Genetics Professionals Toward the Return of Incidental Results from Exome and Whole-Genome Sequencing

Por Yu, Joon-Ho, Harrell, Tanya M., Jamal, Seema M., Tabor, Holly K., Bamshad, Michael J.
Publicado em 2014

DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype

Por Srichomkwun, Panudda, Takamatsu, Junta, Nickerson, Deborah A., Bamshad, Michael J., Chong, Jessica X., Refetoff, Samuel
Publicado no Thyroid (2017)

Human Population Genetic Structure and Inference of Group Membership

Por Bamshad, Michael J., Wooding, Stephen, Watkins, W. Scott, Ostler, Christopher T., Batzer, Mark A., Jorde, Lynn B.
Publicado em 2003

A non-active site SET domain surface crucial for the interaction of MLL1 and the RbBP5-ASH2L heterodimer within MLL family core complexes

Por Shinsky, Stephen A., Hu, Michael, Vought, Valarie E., Ng, Sarah B., Bamshad, Michael J., Shendure, Jay, Cosgrove, Michael S.
Publicado em 2014

The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle

Por Racca, Alice W., Beck, Anita E., McMillin, Margaret J., Korte, F. Steven, Bamshad, Michael J., Regnier, Michael
Publicado no Hum Mol Genet (2015)

Anthropologists' views on race, ancestry, and genetics

Por Wagner, Jennifer K., Yu, Joon‐Ho, Ifekwunigwe, Jayne O., Harrell, Tanya M., Bamshad, Michael J., Royal, Charmaine D.
Publicado no Am J Phys Anthropol (2016)

Single-nucleotide evolutionary constraint scores highlight disease-causing mutations

Por Cooper, Gregory M., Goode, David L., Ng, Sarah B., Sidow, Arend, Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A.
Publicado em 2010