HORIZONS IN PHYSICAL GEOGRAPHY.

Por CLARK, MICHAEL J
Publicado em C198

On soul and conscience: the medical expert and crime. 150 years of forensic medicine in Glasgow

Por Clark, Michael J.
Publicado em 1990

Phonetics Exercises Using the Alvin Experiment-Control Software

Por Hillenbrand, James M., Gayvert, Robert T., Clark, Michael J.
Publicado no J Speech Lang Hear Res (2015)

Perception of sinewave vowels

Por Hillenbrand, James M., Clark, Michael J., Baer, Carter A.
Publicado em 2011

Performance comparison of exome DNA sequencing technologies

Por Clark, Michael J, Chen, Rui, Lam, Hugo Y K, Karczewski, Konrad J, Chen, Rong, Euskirchen, Ghia, Butte, Atul J, Snyder, Michael
Publicado em 2011

De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa

Por Strom, Samuel P., Clark, Michael J., Martinez, Ariadna, Garcia, Sarah, Abelazeem, Amira A., Matynia, Anna, Parikh, Sachin, Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gorin, Michael B.
Publicado no PLoS One (2016)

Detecting and annotating genetic variations using the HugeSeq pipeline

Por Lam, Hugo Y K, Pan, Cuiping, Clark, Michael J, Lacroute, Phil, Chen, Rui, Haraksingh, Rajini, O’Huallachain, Maeve, Gerstein, Mark B, Kidd, Jeffrey M, Bustamante, Carlos D, Snyder, Michael
Publicado no Nat Biotechnol (2012)

Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing

Por Shoemaker, Lorelei D., Clark, Michael J., Patwardhan, Anil, Chandratillake, Gemma, Garcia, Sarah, Chen, Rong, Morgan, Alexander A., Leng, Nan, Kirk, Scott, Chen, Richard, Cook, Douglas J., Snyder, Michael, Steinberg, Gary K.
Publicado no G3 (Bethesda) (2015)

Performance comparison of whole-genome sequencing platforms

Por Lam, Hugo Y K, Clark, Michael J, Chen, Rui, Chen, Rong, Natsoulis, Georges, O’Huallachain, Maeve, Dewey, Frederick E, Habegger, Lukas, Ashley, Euan A, Gerstein, Mark B, Butte, Atul J, Ji, Hanlee P, Snyder, Michael
Publicado em 2011

Identification of inflammatory gene modules based on variations of human endothelial cell responses to oxidized lipids

Por Gargalovic, Peter S., Imura, Minori, Zhang, Bin, Gharavi, Nima M., Clark, Michael J., Pagnon, Joanne, Yang, Wen-Pin, He, Aiqing, Truong, Amy, Patel, Shilpa, Nelson, Stanley F., Horvath, Steve, Berliner, Judith A., Kirchgessner, Todd G., Lusis, Aldons J.
Publicado em 2006

Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

Por Merker, Jason D., Roskin, Krishna M., Ng, Dana, Pan, Cuiping, Fisk, Dianna G., King, Jasmine J., Hoh, Ramona, Stadler, Michael, Okumoto, Lawrence M., Abidi, Parveen, Hewitt, Rhonda, Jones, Carol D., Gojenola, Linda, Clark, Michael J., Zhang, Bing, Cherry, Athena M., George, Tracy I., Snyder, Michael, Boyd, Scott D., Zehnder, James L., Fire, Andrew Z., Gotlib, Jason
Publicado em 2013

Exome Sequencing in 32 Patients with Anophthalmia/Microphthalmia and Developmental Eye Defects

Por Slavotinek, Anne M., Garcia, Sarah T., Chandratillake, Gemma, Bardakjian, Tanya, Ullah, Ehsan, Wu, Di, Umeda, Kyle, Lao, Richard, Tang, Paul Ling-Fung, Wan, Eunice, Madireddy, Lohith, Lyalina, Svetlana, Mendelsohn, Bryce A., Dugan, Sarah, Tirch, Jean, Tischler, Reana, Harris, Jason, Clark, Michael J., Chervitz, Stephen, Patwardhan, Anil, West, John M., Ursell, Phillip, de Alba Campomanes, Alejandra, Schneider, Adele, Kwok, Pui-yan, Baranzini, Sergio, Chen, Richard O.
Publicado no Clin Genet (2015)

Early somatic mosaicism is a rare cause of long-QT syndrome

Por Priest, James Rush, Gawad, Charles, Kahlig, Kristopher M., Yu, Joseph K., O’Hara, Thomas, Boyle, Patrick M., Rajamani, Sridharan, Clark, Michael J., Garcia, Sarah T. K., Ceresnak, Scott, Harris, Jason, Boyle, Sean, Dewey, Frederick E., Malloy-Walton, Lindsey, Dunn, Kyla, Grove, Megan, Perez, Marco V., Neff, Norma F., Chen, Richard, Maeda, Katsuhide, Dubin, Anne, Belardinelli, Luiz, West, John, Antolik, Christian, Macaya, Daniela, Quertermous, Thomas, Trayanova, Natalia A., Quake, Stephen R., Ashley, Euan A.
Publicado no Proc Natl Acad Sci U S A (2016)

Mutations in NGLY1 Cause an Inherited Disorder of the Endoplasmic Reticulum-Associated Degradation (ERAD) Pathway

Por Enns, Gregory M., Shashi, Vandana, Bainbridge, Matthew, Gambello, Michael J., Zahir, Farah R., Bast, Thomas, Crimian, Rebecca, Schoch, Kelly, Platt, Julia, Cox, Rachel, Bernstein, Jonathan, Scavina, Mena, Walter, Rhonda S., Bibb, Audrey, Jones, Melanie, Hegde, Madhuri, Graham, Brett H., Need, Anna C., Oviedo, Angelica, Schaaf, Christian P., Boyle, Sean, Butte, Atul J., Chen, Rong, Clark, Michael J., Haraksingh, Rajini, Cowan, Tina M., He, Ping, Langlois, Sylvie, Zoghbi, Huda Y., Snyder, Michael, Gibbs, Richard, Freeze, Hudson H., Goldstein, David B.
Publicado no Genet Med (2014)

Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

Por Chen, Rui, Mias, George I., Li-Pook-Than, Jennifer, Jiang, Lihua, Lam, Hugo Y. K., Chen, Rong, Miriami, Elana, Karczewski, Konrad J., Hariharan, Manoj, Dewey, Frederick E., Cheng, Yong, Clark, Michael J., Im, Hogune, Habegger, Lukas, Balasubramanian, Suganthi, O'Huallachain, Maeve, Dudley, Joel T., Hillenmeyer, Sara, Haraksingh, Rajini, Sharon, Donald, Euskirchen, Ghia, Lacroute, Phil, Bettinger, Keith, Boyle, Alan P., Kasowski, Maya, Grubert, Fabian, Seki, Scott, Garcia, Marco, Whirl-Carrillo, Michelle, Gallardo, Mercedes, Blasco, Maria A., Greenberg, Peter L., Snyder, Phyllis, Klein, Teri E., Altman, Russ B., Butte, Atul, Ashley, Euan A., Nadeau, Kari C., Gerstein, Mark, Tang, Hua, Snyder, Michael
Publicado em 2012