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A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome., Haaland, Wade C., Scaduto Diane I., Maldonado Mario R., Mansouri Dena L., Nalini Ramaswami, Iyer Dinakar, Patel Sanjeet, Guthikonda Anu, Hampe Christiane S., Balasubramanyam Ashok, et al. , Diabetes care, 2009 May, Volume 32, Issue 5, p.873-7, (2009) Abstract
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome., Margulies, Elliott H., Cooper Gregory M., Asimenos George, Thomas Daryl J., Dewey Colin N., Siepel Adam, Birney Ewan, Keefe Damian, Schwartz Ariel S., Hou Minmei, et al. , Genome research, 2007 Jun, Volume 17, Issue 6, p.760-74, (2007) 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
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease., Ueda, Hironori, Howson Joanna M. M., Esposito Laura, Heward Joanne, Snook Hywel, Chamberlain Giselle, Rainbow Daniel B., Hunter Kara M. D., Smith Annabel N., Di Genova Gianfranco, et al. , Nature, 2003 May 29, Volume 423, Issue 6939, p.506-11, (2003) Abstract
The Cancer Genome Atlas Pan-Cancer analysis project., Chang, Kyle, Creighton Chad J., Davis Caleb F., Donehower Lawrence, Drummond Jennifer, Wheeler David, Ally Adrian, Balasundaram Miruna, Birol Inanc, Butterfield Yaron S. N., et al. , Nature genetics, 2013 Sep 26, Volume 45, Issue 10, p.1113-20, (2013)
Characterization of HPV and host genome interactions in primary head and neck cancers., Parfenov, Michael, Pedamallu Chandra Sekhar, Gehlenborg Nils, Freeman Samuel S., Danilova Ludmila, Bristow Christopher A., Lee Semin, Hadjipanayis Angela G., Ivanova Elena V., Wilkerson Matthew D., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2014 Oct 13, (2014) Abstract
Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways., Palmieri, Michela, Impey Soren, Kang Hyojin, di Ronza Alberto, Pelz Carl, Sardiello Marco, and Ballabio Andrea , Human molecular genetics, 2011 Oct 1, Volume 20, Issue 19, p.3852-66, (2011) Abstract
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies., Khanna, Hemant, Davis Erica E., Murga-Zamalloa Carlos A., Estrada-Cuzcano Alejandro, Lopez Irma, den Hollander Anneke I., Zonneveld Marijke N., Othman Mohammad I., Waseem Naushin, Chakarova Christina F., et al. , Nature genetics, 2009 Jun, Volume 41, Issue 6, p.739-45, (2009) Abstract
Comparative genomics of Ceriporiopsis subvermispora and Phanerochaete chrysosporium provide insight into selective ligninolysis., Fernandez-Fueyo, Elena, Ruiz-Dueñas Francisco J., Ferreira Patricia, Floudas Dimitrios, Hibbett David S., Canessa Paulo, Larrondo Luis F., James Tim Y., Seelenfreund Daniela, Lobos Sergio, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2012 Apr 3, Volume 109, Issue 14, p.5458-63, (2012) Abstract
Comparative phylogenomics and multi-gene cluster analyses of the Citrus Huanglongbing (HLB)-associated bacterium Candidatus Liberibacter., Doddapaneni, Harshavardhan, Liao Huihong, Lin Hong, Bai Xianjin, Zhao Xiaolong, Civerolo Edwin L., Irey Michael, Coletta-Filho Helvecio, and Pietersen Gerhard , BMC research notes, 2008, Volume 1, p.72, (2008) Abstract
The complete genome of an individual by massively parallel DNA sequencing., Wheeler, David A., Srinivasan Maithreyan, Egholm Michael, Shen Yufeng, Chen Lei, McGuire Amy, He Wen, Chen Yi-Ju, Makhijani Vinod, Roth Thomas G., et al. , Nature, 2008 Apr 17, Volume 452, Issue 7189, p.872-6, (2008) Abstract
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing., Wang, Xia, Wang Hui, Sun Vincent, Tuan Han-Fang, Keser Vafa, Wang Keqing, Ren Huanan, Lopez Irma, Zaneveld Jacques E., Siddiqui Sorath, et al. , Journal of medical genetics, 2013 Oct, Volume 50, Issue 10, p.674-88, (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
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
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
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
Demographic history and rare allele sharing among human populations., Gravel, Simon, Henn Brenna M., Gutenkunst Ryan N., Indap Amit R., Marth Gabor T., Clark Andrew G., Yu Fuli, Gibbs Richard A., and Bustamante Carlos D. , Proceedings of the National Academy of Sciences of the United States of America, 2011 Jul 19, Volume 108, Issue 29, p.11983-8, (2011) Abstract
The DNA sequence of human chromosome 7., Hillier, Ladeana W., Fulton Robert S., Fulton Lucinda A., Graves Tina A., Pepin Kymberlie H., Wagner-McPherson Caryn, Layman Dan, Maas Jason, Jaeger Sara, Walker Rebecca, et al. , Nature, 2003 Jul 10, Volume 424, Issue 6945, p.157-64, (2003) Abstract
The DNA sequence of the human X chromosome., Ross, Mark T., Grafham Darren V., Coffey Alison J., Scherer Steven, McLay Kirsten, Muzny Donna, Platzer Matthias, Howell Gareth R., Burrows Christine, Bird Christine P., et al. , Nature, 2005 Mar 17, Volume 434, Issue 7031, p.325-37, (2005) Abstract
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci., Demerath, Ellen W., Guan Weihua, Grove Megan L., Aslibekyan Stella, Mendelson Michael, Zhou Yi-Hui, Hedman Åsa K., Sandling Johanna K., Li Li-An, Irvin Marguerite R., et al. , Human molecular genetics, 2015 Aug 1, Volume 24, Issue 15, p.4464-79, (2015) Abstract
Evolutionary and biomedical insights from the rhesus macaque genome., Gibbs, Richard A., Rogers Jeffrey, Katze Michael G., Bumgarner Roger, Weinstock George M., Mardis Elaine R., Remington Karin A., Strausberg Robert L., Venter Craig J., Wilson Richard K., et al. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.222-34, (2007) Abstract
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling., Chaki, Moumita, Airik Rannar, Ghosh Amiya K., Giles Rachel H., Chen Rui, Slaats Gisela G., Wang Hui, Hurd Toby W., Zhou Weibin, Cluckey Andrew, et al. , Cell, 2012 Aug 3, Volume 150, Issue 3, p.533-48, (2012) Abstract
Fine mapping and identification of candidate pulmonary adenoma susceptibility 1 genes using advanced intercross lines., Wang, Min, Lemon William J., Liu Gongjie, Wang Yian, Iraqi Fuad A., Malkinson Alvin M., and You Ming , Cancer research, 2003 Jun 15, Volume 63, Issue 12, p.3317-24, (2003) Abstract
The finished DNA sequence of human chromosome 12., Scherer, Steven E., Muzny Donna M., Buhay Christian J., Chen Rui, Cree Andrew, Ding Yan, Dugan-Rocha Shannon, Gill Rachel, Gunaratne Preethi, Harris Alan R., et al. , Nature, 2006 Mar 16, Volume 440, Issue 7082, p.346-51, (2006) Abstract
Finishing the euchromatic sequence of the human genome., , Nature, 2004 Oct 21, Volume 431, Issue 7011, p.931-45, (2004) Abstract

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