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Articles from the last few issues of BMC Medical Genetics - Latest Articles

	ALDH1A2 (RALDH2) genetic variation in human congenital heart disease [My Copy] BMC Medical Genetics, Vol. 10 (03 November 2009), 113. by Marilene Pavan, Vivane Ruiz, Fabio Silva, et al.Tiago Sobreira, Roberta Cravo, Michelle Vasconcelos, Livia Marques, Sonia Mesquita, Jose Krieger, Antonio Lopes, Paulo Oliveira, Alexandre Pereira, Jose Xavier-Neto
	PLAUR polymorphisms and lung function in UK smokers [My Copy] BMC Medical Genetics, Vol. 10 (31 October 2009), 112. by Ceri Stewart, Ian Hall, Stuart Parker, et al.Miriam Moffatt, Andrew Wardlaw, Martin Connolly, Charlotte Ruse, Ian Sayers
	Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis [My Copy] BMC Medical Genetics, Vol. 10 (30 October 2009), 111. by Suet N. Chen, Mehmet Cilingiroglu, Joshua Todd, et al.Raffaella Lombardi, James Willerson, Antonio Gotto, Christie Ballantne, A. Marian
	Telomere shortening may be associated with human keloids [My Copy] BMC Medical Genetics, Vol. 10 (28 October 2009), 110. by Bruna De Felice, Robert Wilson, Massimo Nacca
	Variation in cytokine genes can contribute to severity of acetabular osteolysis and risk for revision in patients with ABG I total hip arthroplasty: a genetic association study [My Copy] BMC Medical Genetics, Vol. 10 (27 October 2009), 109. by Jiri Gallo, Frantisek Mrazek, Martin Petrek
	Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study [My Copy] BMC Medical Genetics, Vol. 10 (23 October 2009), 108. by Audrey Chu, Rulan Parekh, Brad Astor, et al.Josef Coresh, Yvette Berthier-Schaad, Michael Smith, Alan Shuldiner, Wen H. Kao
	Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands [My Copy] BMC Medical Genetics, Vol. 10 (23 October 2009), 107. by Karolina Aberg, Feng Dai, Satupaitea Viali, et al.John Tuitele, Guangyun Sun, Subba Indugula, Ranjan Deka, Daniel Weeks, Stephen McGarvey
	Genetic effect of CysLTR2 polymorphisms on its mRNA synthesis and stabilization [My Copy] BMC Medical Genetics, Vol. 10 (20 October 2009), 106. by Jeong-Ah Shin, Hun S. Chang, Se-Min Park, et al.An-Soo Jang, Sung W. Park, Jong S. Park, Soo-Taek Uh, Gune I. Lim, Taiyoun Rhim, Mi-Kyeong Kim, Inseon Choi, Il Y. Chung, Byung L. Park, Hyoung D. Shin, Choon-Sik Park
	Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (13 October 2009), 105. by Rowena Keyser, Lize van der Merwe, Mauritz Venter, et al.Craig Kinnear, Louise Warnich, Jonathan Carr, Soraya Bardien posted by 1 person daforerog
	The role of CACNA1S in predisposition to malignant hyperthermia [My Copy] BMC Medical Genetics, Vol. 10 (13 October 2009), 104. by Danielle Carpenter, Christopher Ringrose, Vincenzo Leo, et al.Andrew Morris, Rachel Robinson, P. Jane Halsall, Philip Hopkins, Marie-Anne Shaw
	Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study [My Copy] BMC Medical Genetics, Vol. 10 (09 October 2009), 103. by Lisa Gallicchio, Howard Chang, Dana Christo, et al.Lucy Thuita, Han Y. Huang, Paul Strickland, Ingo Ruczinski, Sandra Clipp, Kathy Helzlsouer
	Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (2009), 102. by Gregory Matuszek, Zohreh Talebizadeh posted by 2 people mitko daforerog
	Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy? [My Copy] BMC Medical Genetics, Vol. 10 (24 September 2009), 101. by Gui-Sen Li, Guang-Jun Nie, Hong Zhang, Ji-Cheng Lv, Yan Shen, Hai-Yan Wang
	Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B44 or HLAB8 [My Copy] BMC Medical Genetics, Vol. 10 (23 September 2009), 100. by Manda Waldrep, Yingxin Zhuang, Harry Schroeder
	Genetic association study of selected candidate genes (ApoB, LPL, Leptin) and telomere length in obese and hypertensive individuals. [My Copy] BMC Medical Genetics, Vol. 10 (22 September 2009), 99. by Birajalaxmi Das, Nilambari Pawar, Divyalakshmi Saini, M. Seshadri
	Genomewide Association Study for Onset Age in Parkinson Disease. [My Copy] BMC medical genetics, Vol. 10, No. 1. (22 September 2009), 98. by Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, et al.Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio B. Mariani, Anita L. Destefano, Cheryl Halter, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud, Psg-Progeni Investigators And P. Coordinators, Psg-Progeni Molecular Genetic P. Laboratory, Genepd Investigators And I. Coordinators, Genepd Molecular Genetics M. Laboratories posted by 2 people psique daforerog
	Pathogenesis of vestibular schwannoma in ring chromosome 22 [My Copy] BMC Medical Genetics, Vol. 10 (22 September 2009), 97. by Ellen Denayer, Hilde Brems, Paul De Cock, et al.Gareth Evans, Frank Van Calenbergh, Naomi Bowers, Raf Sciot, Maria Debiec-Rychter, Joris Vermeesch, Jean-Pierre Fryns, Eric Legius
	Association analyses of the INSIG2 polymorphism in the obesity and cholesterol levels of Korean populations [My Copy] BMC Medical Genetics, Vol. 10 (22 September 2009), 96. by Seongwon Cha, Imhoi Koo, Sun M. Choi, et al.Byung L. Park, Kil S. Kim, Jae-Ryong Kim, Hyoung D. Shin, Jong Y. Kim
	Two-stage case-control association study of dopamine-related genes and migraine [My Copy] BMC Medical Genetics, Vol. 10 (21 September 2009), 95. by Roser Corominas, Marta Ribases, Montserrat Camina, et al.Ester Cuenca-Leon, Julio Pardo, Susana Boronat, Maria-Jesus Sobrido, Bru Cormand, Alfons Macaya
	Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: The Finnish Diabetes Prevention Study. [My Copy] BMC medical genetics, Vol. 10, No. 1. (21 September 2009) by Titta Salopuro, Leena Pulkkinen, Jaana Lindstrom, et al.Marjukka Kolehmainen, Anna-Maija M. Tolppanen, Johan G. Eriksson, Timo T. Valle, Sirkka Aunola, Pirjo Ilanne-Parikka, Sirkka Keinanen-Kiukaanniemi, Jaakko Tuomilehto, Markku Laakso, Matti Uusitupa posted by 1 person Terkko
	Locations and patterns of meiotic recombination in two-generation pedigrees [My Copy] BMC Medical Genetics, Vol. 10 (17 September 2009), 93. by Jason Ting, Elisha Roberson, Duane Currier, Jonathan Pevsner
	Influences of polymorphic variants of DRD2 and SLC6A3 genes, and their combinations on smoking in Polish population [My Copy] BMC Medical Genetics, Vol. 10 (17 September 2009), 92. by Alicja Sieminska, Krzysztof Buczkowski, Ewa Jassem, Marek Niedoszytko, Ewa Tkacz
	Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study [My Copy] BMC Medical Genetics, Vol. 10 (15 September 2009), 91. by Christiane Wolf, Eugen Gramer, Bertram Muller-Myhsok, et al.Francesca Pasutto, Eva Reinthal, Bernd Wissinger, Nicole Weisschuh
	HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q [My Copy] BMC Medical Genetics, Vol. 10 (15 September 2009), 90. by Sarah Lloyd, Martin Rossor, Nick Fox, Simon Mead, John Collinge
	Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples [My Copy] BMC Medical Genetics, Vol. 10 (14 September 2009), 89. by Bjorn Menten, Katrien Swerts, Barbara Delle Chiaie, et al.Sandra Janssens, Karen Buysse, Jan Philippe, Frank Speleman
	Identification of a region required for TSC1 stability by functional analysis of TSC1 missense mutations found in individuals with tuberous sclerosis complex [My Copy] BMC Medical Genetics, Vol. 10 (11 September 2009), 88. by Melika Mozaffari, Marianne Hoogeveen-Westerveld, David Kwiatkowski, et al.Julian Sampson, Rosemary Ekong, Sue Povey, Johan den Dunnen, Ans van den Ouweland, Dicky Halley, Mark Nellist
	Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2 [My Copy] BMC Medical Genetics, Vol. 10 (11 September 2009), 87. by Veronica Bernard, Martina Minnerop, Katrin Burk, Friedmar Kreuz, Gabriele Gillessen-Kaesbach, Christine Zuehlke
	Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (2009), 86. by Qiuying Sha, Zhaogong Zhang, Jennifer Schymick, Bryan Traynor, Shuanglin Zhang posted by 1 person daforerog
	Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions [My Copy] BMC Medical Genetics, Vol. 10 (03 September 2009), 85. by Margaretha Casselbrant, Ellen Mandel, Jeesun Jung, et al.Robert Ferrell, Kathleen Tekely, Jin Szatkiewicz, Amrita Ray, Daniel Weeks
	A MANBA mutation resulting in residual beta-mannosidase activity associated with severe leukoencephalopathy: a possible pseudodeficiency variant [My Copy] BMC Medical Genetics, Vol. 10 (03 September 2009), 84. by Frederique Sabourdy, Pierre Labauge, de Monica Frostad Riise Stensland, et al.Michele Nieto, Violeta L. Garces, Dimitri Renard, Giovanni Castelnovo, Nicolas de Champfleur, Thierry Levade
	The promoter polymorphism -232C/G of the PCK1 gene is associated with type 2 diabetes in a UK-resident South Asian population [My Copy] BMC Medical Genetics, Vol. 10 (02 September 2009), 83. by Simon Rees, Abigail Britten, Srikanth Bellary, et al.J. O'Hare, Sudhesh Kumar, Anthony Barnett, M. Kelly
	Frequency of single nucleotide polymorphisms in NOD1 gene of Ulcerative colitis patients: a case-control study in the Indian population [My Copy] BMC Medical Genetics, Vol. 10 (01 September 2009), 82. by Ravi Verma, Vineet Ahuja, Jaishree Paul
	Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations. [My Copy] BMC Medical Genetics, Vol. 10 (28 August 2009), 81. by Evelina Mocci, Maria Concas, Manuela Fanciulli, et al.Nicola Pirastu, Mauro Adamo, Valentina Cabras, Cristina Fraumene, Ivana Persico, Alessandro Sassu, Andrea Picciau, Dionigio Prodi, Donatella Serra, Ginevra Biino, Mario Pirastu, Andrea Angius
	Rapid detection of the CYP2A612 hybrid allele by Pyrosequencing technology [My Copy] BMC Medical Genetics*, Vol. 10 (24 August 2009), 80. by Deborah Koontz, Jacqueline Huckins, Antonina Spencer, Margaret Gallagher
	Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sample [My Copy] BMC Medical Genetics, Vol. 10 (19 August 2009), 79. by Geza Nagy, Reka Kovacs-Nagy, Eva Kereszturi, et al.Aniko Somogyi, Anna Szekely, Nora Nemeth, Nora Hosszufalusi, Pal Panczel, Zsolt Ronai, Maria Sasvari-Szekely
	New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease [My Copy] BMC Medical Genetics, Vol. 10 (17 August 2009), 78. by Jitka Stekrova, Jana Reiterova, Stanislava Svobodova, et al.Vera Kebrdlova, Petr Lnenicka, Miroslav Merta, Ondrej Viklicky, Milada Kohoutova
	Common polymorphisms within the NR4A3 locus, encoding the orphan nuclear receptor Nor-1, are associated with enhanced beta-cell function in non-diabetic subjects [My Copy] BMC Medical Genetics, Vol. 10 (14 August 2009), 77. by Peter Weyrich, Harald Staiger, Alena Stancakova, et al.Silke Schafer, Kerstin Kirchhoff, Susanne Ullrich, Felicia Ranta, Baptist Gallwitz, Norbert Stefan, Fausto Machicao, Johanna Kuusisto, Markku Laakso, Andreas Fritsche, Hans-Ulrich Haring
	A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin [My Copy] BMC Medical Genetics, Vol. 10 (12 August 2009), 76. by Muhammad Naeem, Sabeen Sheikh, Wasim Ahmad
	Constitutive RB1 mutation in a child conceived by in vitro fertilization: implications for genetic counseling [My Copy] BMC Medical Genetics, Vol. 10 (29 July 2009), 75. by Raquel Barbosa, Fernando Vargas, Evandro Lucena, Cibele Bonvicino, Hector Seuanez
	Novel Quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis [My Copy] BMC Medical Genetics, Vol. 10 (23 July 2009), 74. by Liyong Wang, Ashley Beecham, Marco Di Tullio, et al.Susan Slifer, Susan Blanton, Tatjana Rundek, Ralph Sacco
	Functional analysis of the C-reactive protein (CRP) gene -717A>G polymorphism associated with coronary heart disease [My Copy] BMC Medical Genetics, Vol. 10 (22 July 2009), 73. by Laiyuan Wang, Xiangfeng Lu, Yun Li, Hongfan Li, Shufeng Chen, Dongfeng Gu
	A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form. [My Copy] BMC Medical Genetics, Vol. 10 (22 July 2009), 72. by Paola Concolino, Enrica Mello, Angelo Minucci, et al.Emiliano Giardina, Cecilia Zuppi, Vincenzo Toscano, Ettore Capoluongo
	Association study between vitamin D receptor gene polymorphisms and asthma in the chinese han population: a case-control study [My Copy] BMC Medical Genetics, Vol. 10 (21 July 2009), 71. by Ahlem Saadi, Guimin Gao, Huaichen Li, Chunhua Wei, Yaoqin Gong, Qiji Liu
	OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background [My Copy] BMC Medical Genetics, Vol. 10 (20 July 2009), 70. by Denis Pierron, Marc Ferre, Christophe Rocher, et al.Arnaud Chevrolier, Pascal Murail, Didier Thoraval, Patrizia Amati-Bonneau, Pascal Reynier, Thierry Letellier
	Mutations in STK11 gene in Czech Peutz-Jeghers patients [My Copy] BMC Medical Genetics, Vol. 10 (19 July 2009), 69. by Peter Vasovcak, Alena Puchmajerova, Jan Roubalik, Anna Krepelova
	No association of CDK5 genetic variants with Alzheimer's disease risk [My Copy] BMC Medical Genetics, Vol. 10 (17 July 2009), 68. by Jose L. Vazquez-Higuera, Ignacio Mateo, Pascual Sanchez-Juan, et al.Eloy Rodriguez-Rodriguez, Jon Infante, Jose Berciano, Onofre Combarros
	Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies [My Copy] BMC Medical Genetics, Vol. 10 (17 July 2009), 67. by Dennis Mook-Kanamori, Sandra de Kort, Cornelia van Duijn, et al.Andre Uitterlinden, Albert Hofman, Henriette Moll, Eric Steegers, Anita Hokken-Koelega, Vincent Jaddoe
	Absence of association between SERPINE2 genetic polymorphisms and chronic obstructive pulmonary disease in Han Chinese: a case-control cohort study [My Copy] BMC Medical Genetics, Vol. 10 (16 July 2009), 66. by Li Zhong, Wei-Ping Fu, Chang Sun, Lu-Ming Dai, Ya-Ping Zhang
	Low frequency of the TIRAP S180L polymorphism in Africa, and its potential role in malaria, sepsis, and leprosy [My Copy] BMC Medical Genetics, Vol. 10 (14 July 2009), 65. by Lutz Hamann, Oliver Kumpf, Ron Schuring, et al.Erkan Alpsoy, George Bedu-Addo, Ulrich Bienzle, Linda Oskam, Frank Mockenhaupt, Ralf Schumann
	Association between ACE Gene I/D polymorphisms and hyperandrogenism in women with Polycystic Ovary Syndrome (PCOS) and controls [My Copy] BMC Medical Genetics, Vol. 10 (14 July 2009), 64. by Jing Sun, Haijian Fan, Yena Che, et al.Yunxia Cao, Xiaoke Wu, Hai-Xiang Sun, Fengjing Liang, Long Yi, Yong Wang

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