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Microarray analysis of somatostatin receptor 5-regulated gene expression profiles in murine pancreas., Patel, Sanjeet G., Zhou Guisheng, Liu Shi-He, Li Min, Jeong Jae-Wook, DeMayo Francesco J., Gingras Marie-Claude, Gibbs Richard A., Fisher William E., and Brunicardi Charles F. , World journal of surgery, 2009 Apr, Volume 33, Issue 4, p.630-7, (2009) Abstract
Evolution of pleiotropy: epistatic interaction pattern supports a mechanistic model underlying variation in genotype-phenotype map., Pavlicev, Mihaela, Norgard Elizabeth A., Fawcett Gloria L., and Cheverud James M. , Journal of experimental zoology. Part B, Molecular and developmental evolution, 2011 Jul 15, Volume 316, Issue 5, p.371-85, (2011) Abstract
The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy., Pehlivan, Davut, Beck Christine R., Okamoto Yuji, Harel Tamar, Akdemir Zeynep H. C., Jhangiani Shalini N., Withers Marjorie A., Goksungur Meryem Tuba, Carvalho Claudia M. B., Czesnik Dirk, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2015 Sep 17, (2015) Abstract
Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia., Pehlivan, Davut, Karaca Ender, Aydin Hatip, Beck Christine R., Gambin Tomasz, Muzny Donna M., Bilge Geckinli B., Karaman Ali, Jhangiani Shalini N., Gibbs Richard A., et al. , European journal of human genetics : EJHG, 2014 Jan 15, (2014) Abstract
Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis., Pehlivan, Davut, Akdemir Zeynep Coban, Karaca Ender, Bayram Yavuz, Jhangiani Shalini, Yildiz Edibe Pembegul, Muzny Donna, Uluc Kayihan, Gibbs Richard A., Elcioglu Nursel, et al. , Human genetics, 2015 Apr 17, (2015) Abstract
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks., Peloso, Gina M., Auer Paul L., Bis Joshua C., Voorman Arend, Morrison Alanna C., Stitziel Nathan O., Brody Jennifer A., Khetarpal Sumeet A., Crosby Jacy R., Fornage Myriam, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.223-32, (2014) Abstract
Tissue-specific transcriptome sequencing analysis expands the non-human primate reference transcriptome resource (NHPRTR)., Peng, Xinxia, Thierry-Mieg Jean, Thierry-Mieg Danielle, Nishida Andrew, Pipes Lenore, Bozinoski Marjan, Thomas Matthew J., Kelly Sara, Weiss Jeffrey M., Raveendran Muthuswamy, et al. , Nucleic acids research, 2014 Nov 11, (2014) Abstract
Open access data sharing in genomic research., Pereira, Stacey, Gibbs Richard A., and McGuire Amy L. , Genes, 2014, Volume 5, Issue 3, p.739-47, (2014) Abstract
Conservation of human chromosome 18 in baboons (Papio hamadryas): a linkage map of eight human microsatellites., Perelygin, A. A., Kammerer C. M., Stowell N. C., and Rogers J. , Cytogenetics and cell genetics, 1996, Volume 75, Issue 4, p.207-9, (1996) Abstract
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype., Perrault, Isabelle, Estrada-Cuzcano Alejandro, Lopez Irma, Kohl Susanne, Li Shiqiang, Testa Francesco, Zekveld-Vroon Renate, Wang Xia, Pomares Esther, Andorf Jean, et al. , PloS one, 2013, Volume 8, Issue 1, p.e51622, (2013) Abstract
cneViewer: a database of conserved non-coding elements for studies of tissue-specific gene regulation., Persampieri, Jason, Ritter Deborah I., Lees Daniel, Lehoczky Jessica, Li Qiang, Guo Su, and Chuang Jeffrey H. , Bioinformatics (Oxford, England), 2008 Oct 15, Volume 24, Issue 20, p.2418-9, (2008) Abstract
Collaborative social and medical service application., Petermann, C. A., Buffone G. J., Bobroff R. B., Moore D. M., Dargahi R., Moreau D. R., Gilson H. S., Li Y., Fowler J., and Beck J. R. , Medinfo. MEDINFO, 1995, Volume 8 Pt 2, p.1671, (1995) Abstract
Collaborative Social and Medical Service System., Petermann, C. A., Bobroff R. B., Moore D. M., Gilson H. S., Li Y., Dargahi R., Classen D. W., Fowler J., Moreau D. R., and Beck J. R. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1994, p.614-8, (1994) Abstract
BCOR-CCNB3 fusions are frequent in undifferentiated sarcomas of male children., Peters, Tricia L., Kumar Vijetha, Polikepahad Sumanth, Lin Frank Y., Sarabia Stephen F., Liang Yu, Wang Wei-Lien, Lazar Alexander J., Doddapaneni Harshavardhan, Chao Hsu, et al. , Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2014 Oct 31, (2014) Abstract
Metagenomic pyrosequencing and microbial identification., Petrosino, Joseph F., Highlander Sarah, Luna Ruth Ann, Gibbs Richard A., and Versalovic James , Clinical chemistry, 2009 May, Volume 55, Issue 5, p.856-66, (2009) Abstract
Chromosome rearrangement and diversification of Francisella tularensis revealed by the type B (OSU18) genome sequence., Petrosino, Joseph F., Xiang Qin, Karpathy Sandor E., Jiang Huaiyang, Yerrapragada Shailaja, Liu Yamei, Gioia Jason, Hemphill Lisa, Gonzalez Arely, Raghavan T. M., et al. , Journal of bacteriology, 2006 Oct, Volume 188, Issue 19, p.6977-85, (2006) Abstract
Whole genome sequence of Treponema pallidum ssp. pallidum, strain Mexico A, suggests recombination between yaws and syphilis strains., Pětrošová, Helena, Zobaníková Marie, Čejková Darina, Mikalová Lenka, Pospíšilová Petra, Strouhal Michal, Chen Lei, Qin Xiang, Muzny Donna M., Weinstock George M., et al. , PLoS neglected tropical diseases, 2012, Volume 6, Issue 9, p.e1832, (2012) Abstract
[Theory of microcirculation. 1: Misinterpretations in Starling's hypothesis of microcirculation]., Petrow, J. M. , Zeitschrift für die gesamte innere Medizin und ihre Grenzgebiete, 1990 Sep 15, Volume 45, Issue 18, p.531-5, (1990)
The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery., Philippakis, Anthony A., Azzariti Danielle R., Beltran Sergi, Brookes Anthony J., Brownstein Catherine A., Brudno Michael, Brunner Han G., Buske Orion J., Carey Knox, Doll Cassie, et al. , Human mutation, 2015 Oct, Volume 36, Issue 10, p.915-21, (2015) Abstract
Genetic contributions to the midsagittal area of the corpus callosum., Phillips, Kimberley A., Rogers Jeffrey, Barrett Elizabeth A., Glahn David C., and Kochunov Peter , Twin research and human genetics : the official journal of the International Society for Twin Studies, 2012 Jun, Volume 15, Issue 3, p.315-23, (2012) Abstract
Why primate models matter., Phillips, Kimberley A., Bales Karen L., Capitanio John P., Conley Alan, Czoty Paul W., 't Hart Bert A., Hopkins William D., Hu Shiu-Lok, Miller Lisa A., Nader Michael A., et al. , American journal of primatology, 2014 Apr 10, (2014) Abstract
Mutational landscape of aggressive cutaneous squamous cell carcinoma., Pickering, Curtis R., Zhou Jane H., Lee Jack J., Drummond Jennifer A., Peng Andrew S., Saade Rami E., Tsai Kenneth Y., Curry Jonathan, Tetzlaff Michael T., Lai Stephen Y., et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2014 Oct 10, (2014) Abstract
Squamous Cell Carcinoma of the Oral Tongue in Young Non-Smokers Is Genomically Similar to Tumors in Older Smokers, Pickering, C. R., Zhang J., Neskey D. M., Zhao M., Jasser S. A., Wang J., Ward A., Tsai C. J., Ortega Alves M. V., Zhou J. H., et al. , Clinical Cancer Research, 07/2014, Volume 20, Issue 14, p.3842 - 3848, (2014)
Integrative genomic characterization of oral squamous cell carcinoma identifies frequent somatic drivers., Pickering, Curtis R., Zhang Jiexin, Yoo Suk Young, Bengtsson Linnea, Moorthy Shhyam, Neskey David M., Zhao Mei, Ortega Alves Marcus V., Chang Kyle, Drummond Jennifer, et al. , Cancer discovery, 2013 Jul, Volume 3, Issue 7, p.770-81, (2013) Abstract
A transposon-like element in the deletion-prone region of the dystrophin gene., Pizzuti, A., Pieretti M., Fenwick R. G., Gibbs R. A., and Caskey C. T. , Genomics, 1992 Jul, Volume 13, Issue 3, p.594-600, (1992) Abstract

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