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Nature Biotechnology, ISSN 1087-0156, 06/2011, Volume 29, Issue 6, pp. 512 - 520
Journal Article
Current Protocols in Human Genetics, ISSN 1934-8266, 04/2010, Volume Chapter 4, Issue 65, pp. 4.14.1 - 4.14.28
Journal Article
Journal Article
by Altshuler, David M and Gibbs, Richard A and Peltonen, Leena and Schaffner, Stephen F and Yu, Fuli and Dermitzakis, Emmanouil and Bonnen, Penelope E and De Bakker, Paul I. W and Deloukas, Panos and Gabriel, Stacey B and Gwilliam, Rhian and Hunt, Sarah and Inouye, Michael and Jia, Xiaoming and Aarno Palotie, Palotie and Parkin, Melissa and Whittaker, Pamela and Chang, Kyle and Hawes, Alicia and Lewis, Lora R and Ren, Yanru and Wheeler, David and Muzny, Donna Marie and Barnes, Chris and Darvishi, Katayoon and Hurles, Matthew and Korn, Joshua M and Kristiansson, Kati and Lee, Charles and McCarroll, Steven A and Nemesh, James and Keinan, Alon and Montgomery, Stephen B and Samuela Pollack, Pollack and Price, Alkes L and Soranzo, Nicole and Gonzaga-Jauregui, Claudia and Anttila, Verneri and Brodeur, Wendy and Daly, Mark J and Leslie, Stephen and McVean, Gil and Moutsianas, Loukas and Nguyen, Huy and Zhang, Qingrun and Ghori, Mohammed J. R and McGinnis, Ralph and McLaren, William and Pollack, Samuela and Takeuchi, Fumihiko and Grossman, Sharon R and Shlyakhter, Ilya and Hostetter, Elizabeth B and Sabeti, Pardis C and Adebamowo, Clement A and Foster, Morris W and Gordon, Deborah R and Licinio, Julio and Manca, Maria Cristina and Marshall, Patricia A and Matsuda, Ichiro and Ngare, Duncan and Wang, Vivian Ota and Reddy, Deepa and Rotimi, Charles N and Royal, Charmaine D and Sharp, Richard R and Zeng, Changqing and Brooks, D.B and McEwen, Jean E and Int HapMap 3 Consortium and The International HapMap 3 Consortium
Nature, ISSN 0028-0836, 09/2010, Volume 467, Issue 7311, pp. 52 - 58
Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding... 
DISEASES | POSITIVE SELECTION | VARIANTS | HAPLOTYPE MAP | MULTIDISCIPLINARY SCIENCES | REGIONS | SIGNALS | SNPS | COPY NUMBER VARIATION | GENOME-WIDE ASSOCIATION | Human genome | Genetic variation | Research | Genetics | Algorithms | Genetic testing | Genomics | Quality control
Journal Article
ISSN 1471-2105, 2013
Background: In recent years there has been a growing interest in the role of copy number variations (CNV) in genetic diseases. Though there has been rapid... 
Genetics | Statistics
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 04/2006, Volume 14, Issue 4, pp. 438 - 442
Single nucleotide polymorphisms (SNPs) in the regulatory region shared by PARK2 and PACRG have been identified as major risk factors for leprosy susceptibility... 
Indian | PACRG | SNP | PARK2 | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY | GENETICS & HEREDITY | Haplotypes | Genetic Predisposition to Disease | Gene Frequency | Humans | Middle Aged | Regulatory Sequences, Nucleic Acid | Molecular Chaperones - genetics | Male | India | Adolescent | Adult | Female | Polymorphism, Single Nucleotide | Ubiquitin-Protein Ligases - genetics | Leprosy - genetics
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 07/2014, Volume 59, Issue 7, pp. 415 - 416
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 06/2011, Volume 52, Issue 6, pp. 1139 - 1149
Journal Article