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Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay., Hardenbol, Paul, Yu Fuli, Belmont John, Mackenzie Jennifer, Bruckner Carsten, Brundage Tiffany, Boudreau Andrew, Chow Steve, Eberle Jim, Erbilgin Ayca, et al. , Genome research, 2005 Feb, Volume 15, Issue 2, p.269-75, (2005) Abstract
Homozygous loss-of-function mutations in SOHLH1 in patients with non-syndromic hypergonadotropic hypogonadism., Bayram, Yavuz, Gulsuner Suleyman, Guran Tulay, Abaci Ayhan, Yesil Gozde, Gulsuner Hilal Unal, Atay Zeynep, Pierce Sarah B., Gambin Tomasz, Lee Ming, et al. , The Journal of clinical endocrinology and metabolism, 2015 Mar 16, p.jc20151150, (2015) Abstract
A homozygous missense mutation in NEUROD1 is associated with non-syndromic autosomal recessive retinitis pigmentosa., Wang, Feng, Li Huajin, Xu Mingchu, Li Hui, Zhao Li, Yang Lizhu, Zaneveld Jacques E., Wang Keqing, Li Yumei, Sui Ruifang, et al. , Investigative ophthalmology & visual science, 2014 Dec 4, (2014) Abstract
Horizontal gene transfer in cyanobacterial signature genes., Yerrapragada, Shailaja, Siefert Janet L., and Fox George E. , Methods in molecular biology (Clifton, N.J.), 2009, Volume 532, p.339-66, (2009) Abstract
How is the Drosophila research community making use of the genome sequence?, Richards, Stephen , Genome biology, 2003, Volume 4, Issue 5, p.319, (2003) Abstract
Hsp90 modulates CAG repeat instability in human cells., Mittelman, David, Sykoudis Kristen, Hersh Megan, Lin Yunfu, and Wilson John H. , Cell stress & chaperones, 2010 Sep, Volume 15, Issue 5, p.753-9, (2010) Abstract
Human adipose tissue as a reservoir for memory CD4+ T cells and HIV., Couturier, Jacob, Suliburk James W., Brown Jeremy M., Luke David J., Agarwal Neeti, Yu Xiaoying, Nguyen Chi, Iyer Dinakar, Kozinetz Claudia A., Overbeek Paul A., et al. , AIDS (London, England), 2015 Mar 27, Volume 29, Issue 6, p.667-74, (2015) Abstract
Human CLP1 Mutations Alter tRNA Biogenesis, Affecting Both Peripheral and Central Nervous System Function., Karaca, Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos, Hanada Toshikatsu, Jhangiani Shalini N., Wiszniewski Wojciech, Withers Marjorie, Campbell Ian M., et al. , Cell, 2014 Apr 24, Volume 157, Issue 3, p.636-50, (2014) Abstract
The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs., Reiter, L. T., Murakami T., Koeuth T., Gibbs R. A., and Lupski J. R. , Human molecular genetics, 1997 Sep, Volume 6, Issue 9, p.1595-603, (1997) Abstract
A human dimorphism resulting from loss of an Alu., Edwards, M. C., and Gibbs R. A. , Genomics, 1992 Nov, Volume 14, Issue 3, p.590-7, (1992) Abstract
Human genetics. Primate shadow play., Gibbs, Richard A., and Nelson David L. , Science (New York, N.Y.), 2003 Feb 28, Volume 299, Issue 5611, p.1331-3, (2003)
Human genome sequencing in health and disease., Gonzaga-Jauregui, Claudia, Lupski James R., and Gibbs Richard A. , Annual review of medicine, 2012, Volume 63, p.35-61, (2012) Abstract
The human genome: genes, pseudogenes, and variation on chromosome 7., Waterston, R. H., Hillier L. W., Fulton L. A., Fulton R. S., Graves T. A., Pepin K. H., Bork P., Suyama M., Torrents D., Chinwalla A. T., et al. , Cold Spring Harbor symposia on quantitative biology, 2003, Volume 68, p.13-22, (2003)
Human Lymphatic Architecture and Dynamic Transport Imaged Using Near-infrared Fluorescence., Rasmussen, John C., Tan I-Chih, Marshall Milton V., Adams Kristen E., Kwon Sunkuk, Fife Caroline E., Maus Erik A., Smith Latisha A., Covington Kyle R., and Sevick-Muraca Eva M. , Translational oncology, 2010, Volume 3, Issue 6, p.362-72, (2010) Abstract
Human Metabolome Associates With Dietary Intake Habits Among African Americans in the Atherosclerosis Risk in Communities Study., Zheng, Yan, Yu Bing, Alexander Danny, Steffen Lyn M., and Boerwinkle Eric , American journal of epidemiology, 2014 May 6, (2014) Abstract
The human transcript database: a catalogue of full length cDNA inserts., Bouck, J., McLeod M. P., Worley K., and Gibbs R. A. , Bioinformatics (Oxford, England), 2000 Feb, Volume 16, Issue 2, p.176-7, (2000) Abstract
The human transcript database: a catalogue of full length cDNA inserts., Bouck, J., McLeod M. P., Worley K., and Gibbs R. A. , Bioinformatics (Oxford, England), 2000 Feb, Volume 16, Issue 2, p.176-7, (2000) Abstract
Human-specific changes of genome structure detected by genomic triangulation., Harris, R. A., Rogers J., and Milosavljevic A. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.235-7, (2007) Abstract
Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death., Boone, Philip M., Yuan Bo, Gu Shen, Ma Zhiwei, Gambin Tomasz, Gonzaga-Jauregui Claudia, Jain Mahim, Murdock Todd J., White Janson J., Jhangiani Shalini N., et al. , Molecular genetics & genomic medicine, 2016 Jan, Volume 4, Issue 1, p.77-94, (2016) Abstract
Hypermutagenesis in mutA cells is mediated by mistranslational corruption of polymerase, and is accompanied by replication fork collapse., Al Mamun, Abu Amar M., Gautam Satyendra, and Humayun Zafri M. , Molecular microbiology, 2006 Dec, Volume 62, Issue 6, p.1752-63, (2006) Abstract
The hypofunctional effect of P335L single nucleotide polymorphism on SSTR5 function., Zhou, Guisheng, Gingras Marie-Claude, Liu Shi-He, Li Donghui, Li Zhijun, Catania Robbi L., Stehling Kelly M., Li Min, Paganelli Giovanni, Gibbs Richard A., et al. , World journal of surgery, 2011 Aug, Volume 35, Issue 8, p.1715-24, (2011) Abstract
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1., Soens, Zachry T., Li Yuanyuan, Zhao Li, Eblimit Aiden, Dharmat Rachayata, Li Yumei, Chen Yiyun, Naqeeb Mohammed, Fajardo Norma, Lopez Irma, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2016 Jan 28, (2016) Abstract


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