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D
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors., Parsons, Williams D., Roy Angshumoy, Yang Yaping, Wang Tao, Scollon Sarah, Bergstrom Katie, Kerstein Robin A., Gutierrez Stephanie, Petersen Andrea K., Bavle Abhishek, et al. , JAMA oncology, 2016 Jan 28, (2016) Abstract
Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study., Meyer, Tamra E., Boerwinkle Eric, Morrison Alanna C., Volcik Kelly A., Sanderson Maureen, Coker Ann L., Pankow James S., and Folsom Aaron R. , Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2010 Feb, Volume 19, Issue 2, p.558-65, (2010) Abstract
Detection of clinically relevant copy number variants with whole-exome sequencing., de Ligt, Joep, Boone Philip M., Pfundt Rolph, Vissers Lisenka E. L. M., Richmond Todd, Geoghegan Joel, O'Moore Kathleen, de Leeuw Nicole, Shaw Christine, Brunner Han G., et al. , Human mutation, 2013 Oct, Volume 34, Issue 10, p.1439-48, (2013) Abstract
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy., Yang, Zhao, Bowles Neil E., Scherer Steven E., Taylor Michael D., Kearney Debra L., Ge Shuping, Nadvoretskiy Vyacheslav V., DeFreitas Gilberto, Carabello Blasé, Brandon Lois I., et al. , Circulation research, 2006 Sep 15, Volume 99, Issue 6, p.646-55, (2006) Abstract
Designing new microsatellite markers for linkage and population genetic analyses in rhesus macaques and other nonhuman primates., Raveendran, Muthuswamy, Harris Alan R., Milosavljevic Aleksandar, Johnson Zach, Shelledy Wendy, Cameron Judy, and Rogers Jeffrey , Genomics, 2006 Dec, Volume 88, Issue 6, p.706-10, (2006) Abstract
Demographic, environmental, and genetic predictors of metabolic side effects of hydrochlorothiazide treatment in hypertensive subjects., Maitland-van der Zee, Anke-Hilse, Turner Stephen T., Schwartz Gary L., Chapman Arlene B., Klungel Olaf H., and Boerwinkle Eric , American journal of hypertension, 2005 Aug, Volume 18, Issue 8, p.1077-83, (2005) Abstract
Demographic histories and patterns of linkage disequilibrium in Chinese and Indian rhesus macaques., Hernandez, Ryan D., Hubisz Melissa J., Wheeler David A., Smith David G., Ferguson Betsy, Rogers Jeffrey, Nazareth Lynne, Indap Amit, Bourquin Traci, McPherson John, et al. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.240-3, (2007) Abstract
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles., Boone, Philip M., Campbell Ian M., Baggett Brett C., Soens Zachry T., Rao Mitchell M., Hixson Patricia M., Patel Ankita, Bi Weimin, Cheung Sau Wai, Lalani Seema R., et al. , Genome research, 2013 Sep, Volume 23, Issue 9, p.1383-94, (2013) Abstract
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome., Koekkoek, S. K. E., Yamaguchi K., Milojkovic B. A., Dortland B. R., Ruigrok T. J. H., Maex R., De Graaf W., Smit A. E., VanderWerf F., Bakker C. E., et al. , Neuron, 2005 Aug 4, Volume 47, Issue 3, p.339-52, (2005) Abstract
Deep resequencing reveals excess rare recent variants consistent with explosive population growth., Coventry, Alex, Bull-Otterson Lara M., Liu Xiaoming, Clark Andrew G., Maxwell Taylor J., Crosby Jacy, Hixson James E., Rea Thomas J., Muzny Donna M., Lewis Lora R., et al. , Nature communications, 2010, Volume 1, p.131, (2010) Abstract
Deep resequencing and association analysis of schizophrenia candidate genes., Crowley, J. J., Hilliard C. E., Kim Y., Morgan M. B., Lewis L. R., Muzny D. M., Hawes A. C., Sabo A., Wheeler D. A., Lieberman J. A., et al. , Molecular psychiatry, 2013 Feb, Volume 18, Issue 2, p.138-40, (2013)
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy., Fu, Y. H., Friedman D. L., Richards S., Pearlman J. A., Gibbs R. A., Pizzuti A., Ashizawa T., Perryman M. B., Scarlato G., and Fenwick R. G. , Science (New York, N.Y.), 1993 Apr 9, Volume 260, Issue 5105, p.235-8, (1993) Abstract
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome., Bainbridge, Matthew N., Hu Hao, Muzny Donna M., Musante Luciana, Lupski James R., Graham Brett H., Chen Wei, Gripp Karen W., Jenny Kim, Wienker Thomas F., et al. , Genome medicine, 2013 Feb 5, Volume 5, Issue 2, p.11, (2013) Abstract
De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea., Xia, Fan, Bainbridge Matthew N., Tan Tiong Yang, Wangler Michael F., Scheuerle Angela E., Zackai Elaine H., Harr Margaret H., Sutton Reid V., Nalam Roopa L., Zhu Wenmiao, et al. , American journal of human genetics, 2014 May 1, Volume 94, Issue 5, p.784-9, (2014) Abstract
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome., Burrage, Lindsay C., Charng Wu-Lin, Eldomery Mohammad K., Willer Jason R., Davis Erica E., Lugtenberg Dorien, Zhu Wenmiao, Leduc Magalie S., Akdemir Zeynep C., Azamian Mahshid, et al. , American journal of human genetics, 2015 Dec 3, Volume 97, Issue 6, p.904-13, (2015) Abstract
C
Cyanophora paradoxa genome elucidates origin of photosynthesis in algae and plants., Price, Dana C., Chan Cheong Xin, Yoon Hwan Su, Yang Eun Chan, Qiu Huan, Weber Andreas P. M., Schwacke Rainer, Gross Jeferson, Blouin Nicolas A., Lane Chris, et al. , Science (New York, N.Y.), 2012 Feb 17, Volume 335, Issue 6070, p.843-7, (2012) Abstract
Cyanobacterial signature genes., Martin, Kirt A., Siefert Janet L., Yerrapragada Sailaja, Lu Yue, McNeill Thomas Z., Moreno Pedro A., Weinstock George M., Widger William R., and Fox George E. , Photosynthesis research, 2003, Volume 75, Issue 3, p.211-21, (2003) Abstract
CRHR1 genotypes, neural circuits and the diathesis for anxiety and depression., Rogers, J., Raveendran M., Fawcett G. L., Fox A. S., Shelton S. E., Oler J. A., Cheverud J., Muzny D. M., Gibbs R. A., Davidson R. J., et al. , Molecular psychiatry, 2013 Jun, Volume 18, Issue 6, p.700-7, (2013) Abstract
CRHR1 genotypes, neural circuits and the diathesis for anxiety and depression., Rogers, J., Raveendran M., Fawcett G. L., Fox A. S., Shelton S. E., Oler J. A., Cheverud J., Muzny D. M., Gibbs R. A., Davidson R. J., et al. , Molecular psychiatry, 2013 Jun, Volume 18, Issue 6, p.700-7, (2013) Abstract
Corticotropin releasing hormone (CRH) gene variation: comprehensive resequencing for variant and molecular haplotype discovery in monosomic hybrid cell lines., Shimmin, Lawrence C., Natarajan Sivamani, Ibarguen Heladio, Montasser May, Kim Do-Kyun, Hanis Craig L., Boerwinkle Eric, Wadhwa Pathik D., and Hixson James E. , DNA sequence : the journal of DNA sequencing and mapping, 2007 Dec, Volume 18, Issue 6, p.434-44, (2007) Abstract
Cortical sulcal areas in baboons (Papio hamadryas spp.) with generalized interictal epileptic discharges on scalp EEG., Szabó, C. A., Kochunov P., Knape K. D., McCoy K. J. M., Leland M. M., Lancaster J. L., Fox P. T., Williams J. T., and Rogers J. , Epilepsy research, 2011 Feb, Volume 93, Issue 2-3, p.91-5, (2011) Abstract
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta)., Degenhardt, Jeremiah D., de Candia Paola, Chabot Adrien, Schwartz Stuart, Henderson Les, Ling Binhua, Hunter Meredith, Jiang Zhaoshi, Palermo Robert E., Katze Michael, et al. , PLoS genetics, 2009 Jan, Volume 5, Issue 1, p.e1000346, (2009) Abstract
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis., Watkin, Levi B., Jessen Birthe, Wiszniewski Wojciech, Vece Timothy J., Jan Max, Sha Youbao, Thamsen Maike, Santos-Cortez Regie L. P., Lee Kwanghyuk, Gambin Tomasz, et al. , Nature genetics, 2015 Apr 20, (2015) Abstract
Cooperation between the TNF receptors demonstrated by TNF receptor knockout mice, Shinbrot, Eve, and Moore Mark , Cytokine Knockouts. Humana Press, New Jersey, Volume 89, (1998)
Construction of small genome BAC library for functional and genomic applications., Smajs, David, Norris Steven J., and Weinstock George M. , Methods in molecular biology (Clifton, N.J.), 2004, Volume 255, p.47-56, (2004)


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