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Neutral mitochondrial heteroplasmy and the influence of aging
Sondheimer, Neal, Glatz, Catherine E., Tirone, Jack E., Deardorff, Matthew A., Krieger, Abba M., Hakonarson, Hakon
Published in Human molecular genetics (15.04.2011)
Published in Human molecular genetics (15.04.2011)
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Reptilian heart development and the molecular basis of cardiac chamber evolution
Koshiba-Takeuchi, Kazuko, Mori, Alessandro D., Kaynak, Bogac L., Cebra-Thomas, Judith, Sukonnik, Tatyana, Georges, Romain O., Latham, Stephany, Beck, Laural, Henkelman, R. Mark, Black, Brian L., Olson, Eric N., Wade, Juli, Takeuchi, Jun K., Nemer, Mona, Gilbert, Scott F., Bruneau, Benoit G.
Published in Nature (London) (03.09.2009)
Published in Nature (London) (03.09.2009)
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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
Simon-Sanchez, Javier, Scholz, Sonja, Fung, Hon-Chung, Matarin, Mar, Hernandez, Dena, Gibbs, J. Raphael, Britton, Angela, de Vrieze, Fabienne Wavrant, Peckham, Elizabeth, Gwinn-Hardy, Katrina, Crawley, Anthony, Keen, Judith C., Nash, Josefina, Borgaonkar, Digamber, Hardy, John, Singleton, Andrew
Published in Human molecular genetics (01.01.2007)
Published in Human molecular genetics (01.01.2007)
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Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder
Etain, Bruno, Dumaine, Anne, Bellivier, Frank, Pagan, Cécile, Francelle, Laetitia, Goubran-Botros, Hany, Moreno, Sarah, Deshommes, Jasmine, Moustafa, Khaled, Le Dudal, Katia, Mathieu, Flavie, Henry, Chantal, Kahn, Jean-Pierre, Launay, Jean-Marie, Mühleisen, Thomas W., Cichon, Sven, Bourgeron, Thomas, Leboyer, Marion, Jamain, Stéphane
Published in Human molecular genetics (15.09.2012)
Published in Human molecular genetics (15.09.2012)
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Comparison of molecular species identification for North Sea calanoid copepods (Crustacea) using proteome fingerprints and DNA sequences
Laakmann, S., Gerdts, G., Erler, R., Knebelsberger, T., Martínez Arbizu, P., Raupach, M.J.
Published in Molecular ecology resources (01.09.2013)
Published in Molecular ecology resources (01.09.2013)
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A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12
Asher, Julian E., Lamb, Janine A., Brocklebank, Denise, Cazier, Jean-Baptiste, Maestrini, Elena, Addis, Laura, Sen, Mallika, Baron-Cohen, Simon, Monaco, Anthony P.
Published in American journal of human genetics (13.02.2009)
Published in American journal of human genetics (13.02.2009)
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Shugoshins: from protectors of cohesion to versatile adaptors at the centromere
Gutiérrez-Caballero, Cristina, Cebollero, Luis R., Pendás, Alberto M.
Published in Trends in genetics (01.07.2012)
Published in Trends in genetics (01.07.2012)
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Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations
Purevjav, Enkhsaikhan, Arimura, Takuro, Augustin, Sibylle, Huby, Anne-Cecile, Takagi, Ken, Nunoda, Shinichi, Kearney, Debra L., Taylor, Michael D., Terasaki, Fumio, Bos, Johan M., Ommen, Steve R., Shibata, Hiroki, Takahashi, Megumi, Itoh-Satoh, Manatsu, McKenna, William J., Murphy, Ross T., Labeit, Siegfried, Yamanaka, Yoichi, Machida, Noboru, Park, Jeong-Euy, Alexander, Peta M.A., Weintraub, Robert G., Kitaura, Yasushi, Ackerman, Michael J., Kimura, Akinori, Towbin, Jeffrey A.
Published in Human molecular genetics (01.05.2012)
Published in Human molecular genetics (01.05.2012)
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Sarcoidosis HLA class II genotyping distinguishes differences of clinical phenotype across ethnic groups
Sato, Hiroe, Woodhead, Felix A., Ahmad, Tariq, Grutters, Jan C., Spagnolo, Paolo, van den Bosch, Jules M.M., Maier, Lisa A., Newman, Lee S., Nagai, Sonoko, Izumi, Takateru, Wells, Athol U., du Bois, Roland M., Welsh, Kenneth I.
Published in Human molecular genetics (15.10.2010)
Published in Human molecular genetics (15.10.2010)
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Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization
Twigg, Stephen R.F., Lloyd, Deborah, Jenkins, Dagan, Elçioglu, Nursel E., Cooper, Christopher D.O., Al-Sannaa, Nouriya, Annagür, Ali, Gillessen-Kaesbach, Gabriele, Hüning, Irina, Knight, Samantha J.L., Goodship, Judith A., Keavney, Bernard D., Beales, Philip L., Gileadi, Opher, McGowan, Simon J., Wilkie, Andrew O.M.
Published in American journal of human genetics (02.11.2012)
Published in American journal of human genetics (02.11.2012)
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A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population
Tan, Aihua, Sun, Jielin, Xia, Ning, Qin, Xue, Hu, Yanling, Zhang, Shijun, Tao, Sha, Gao, Yong, Yang, Xiaobo, Zhang, Haiying, Kim, Seong-Tae, Peng, Tao, Lin, Xiaoling, Li, Li, Mo, Linjian, Liang, Zhengjia, Shi, Deyi, Huang, Zhang, Huang, Xianghua, Liu, Ming, Ding, Qiang, Trent, Jeffrey M, Zheng, S. Lilly, Mo, Zengnan, Xu, Jianfeng
Published in Human molecular genetics (01.04.2012)
Published in Human molecular genetics (01.04.2012)
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Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
Simpson, M.A., Hsu, R., Keir, L.S., Hao, J., Sivapalan, G., Ernst, L.M., Zackai, E.H., Al-Gazali, L.I., Hulskamp, G., Kingston, H.M., Prescott, T.E., Ion, A., Patton, M.A., Murday, V., George, A., Crosby, A.H.
Published in American journal of human genetics (01.11.2007)
Published in American journal of human genetics (01.11.2007)
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Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia
Péterfy, Miklós, Ben-Zeev, Osnat, Mao, Hui Z, Weissglas-Volkov, Daphna, Aouizerat, Bradley E, Pullinger, Clive R, Frost, Philip H, Kane, John P, Malloy, Mary J, Reue, Karen, Pajukanta, Päivi, Doolittle, Mark H
Published in Nature genetics (01.12.2007)
Published in Nature genetics (01.12.2007)
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Trisomy for Synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes
Cossec, Jack-Christophe, Lavaur, Jérémie, Berman, Diego E., Rivals, Isabelle, Hoischen, Alexander, Stora, Samantha, Ripoll, Clémentine, Mircher, Clotilde, Grattau, Yann, OlivoMarin, Jean-Christophe, de Chaumont, Fabrice, Lecourtois, Magalie, Antonarakis, Stylianos E., Veltman, Joris A., Delabar, Jean M., Duyckaerts, Charles, Di Paolo, Gilbert, Potier, Marie-Claude
Published in Human molecular genetics (15.07.2012)
Published in Human molecular genetics (15.07.2012)
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A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia
Zhao, Han, Xu, Jianfeng, Zhang, Haobo, Sun, Jielin, Sun, Yingpu, Wang, Zhong, Liu, Jiayin, Ding, Qiang, Lu, Shaoming, Shi, Rong, You, Li, Qin, Yingying, Zhao, Xiaoming, Lin, Xiaoling, Li, Xiao, Feng, Junjie, Wang, Li, Trent, Jeffrey M., Xu, Chengyan, Gao, Ying, Zhang, Bo, Gao, Xuan, Hu, Jingmei, Chen, Hong, Li, Guangyu, Zhao, Junzhao, Zou, Shuhua, Jiang, Hong, Hao, Cuifang, Zhao, Yueran, Ma, Jinglong, Zheng, S. Lilly, Chen, Zi-Jiang
Published in American journal of human genetics (04.05.2012)
Published in American journal of human genetics (04.05.2012)
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Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
Bassett, Anne S., Marshall, Christian R., Lionel, Anath C., Chow, Eva W.C., Scherer, Stephen W.
Published in Human molecular genetics (15.12.2008)
Published in Human molecular genetics (15.12.2008)
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Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus
Okada, Yukinori, Takahashi, Atsushi, Ohmiya, Hiroko, Kumasaka, Natsuhiko, Kamatani, Yoichiro, Hosono, Naoya, Tsunoda, Tatsuhiko, Matsuda, Koichi, Tanaka, Toshihiro, Kubo, Michiaki, Nakamura, Yusuke, Yamamoto, Kazuhiko, Kamatani, Naoyuki
Published in Human molecular genetics (15.03.2011)
Published in Human molecular genetics (15.03.2011)
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The transforming growth factor-β1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD)
Celedón, Juan C., Lange, Christoph, Raby, Benjamin A., Litonjua, Augusto A., Palmer, Lyle J., DeMeo, Dawn L., Reilly, John J., Kwiatkowski, David J., Chapman, Harold A., Laird, Nan, Sylvia, Jody S., Hernandez, Melvin, Speizer, Frank E., Weiss, Scott T., Silverman, Edwin K.
Published in Human molecular genetics (01.08.2004)
Published in Human molecular genetics (01.08.2004)
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