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

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	PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism. [My Copy] BMC medical genetics, Vol. 10, No. 1. (26 December 2009), 146. by Matthew T. Bishop, Catherine Pennington, Craig A. Heath, Robert G. Will, Richard Sg S. Knight posted by 1 person applebyb
	PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women [My Copy] BMC Medical Genetics, Vol. 10 (23 December 2009), 145. by Stephane Cauchi, Inger Byrjalsen, Emmanuelle Durand, Morten Karsdal, Philippe Froguel
	BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1 [My Copy] BMC Medical Genetics, Vol. 10 (23 December 2009), 144. by Anna Brunet, Lluis Armengol, Damia Heine, et al.Jordi Rosell, Manel Garcia-Aragones, Elisabeth Gabau, Xavier Estivill, Miriam Guitart
	A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans [My Copy] BMC Medical Genetics, Vol. 10 (22 December 2009), 143. by Ranjan Deka, Ling Xu, Prodipto Pal, et al.Palanitina Toelupe, Tuiasina Laumoli, Huifeng Xi, Ge Zhang, Daniel Weeks, Stephen McGarvey
	Use of supplementary phenotype to identify additional rheumatoid arthritis loci in a linkage analysis of 342 UK affected sibling pair families [My Copy] BMC Medical Genetics, Vol. 10 (21 December 2009), 142. by Bamidele Tayo, Yulan Liang, Arpad Kelemen, Austin Miller, Maurizio Trevisan, Richard Cooper
	Association of a functional microsatellite within intron 1 of the BMP5 gene with susceptibility to osteoarthritis [My Copy] BMC Medical Genetics, Vol. 10 (19 December 2009), 141. by James Wilkins, Lorraine Southam, Zehra Mustafa, Kay Chapman, John Loughlin
	Melusin gene (ITGB1BP2) nucleotide variations study in hypertensive and cardiopathic patients [My Copy] BMC Medical Genetics, Vol. 10 (17 December 2009), 140. by Valeria Palumbo, Ludovica Segat, Lara Padovan, et al.Antonio Amoroso, Bruno Trimarco, Raffaele Izzo, Giuseppe Lembo, Vera R. Zagrosek, Ralph Knoll, Mara Brancaccio, Guido Tarone, Sergio Crovella
	Association between CYP19 gene SNP rs2414096 Polymorphism and polycystic ovary syndrome in Chinese women [My Copy] BMC Medical Genetics, Vol. 10 (16 December 2009), 139. by Jia-Li Jin, Jing Sun, Hui-juan Ge, et al.Yun-Xia Cao, Xiao-Ke Wu, Feng-Jing Liang, Hai-Xiang Sun, Lu Ke, Long Yi, Zhi-Wei Wu, Yong Wang
	Innate immunity in ocular Chlamydia trachomatis infection: contribution of IL8 and CSF2 gene variants to risk of trachomatous scarring in Gambians [My Copy] BMC Medical Genetics, Vol. 10 (16 December 2009), 138. by Angels Natividad, Jeremy Hull, Gaia Luoni, et al.Martin Holland, Kirk Rockett, Hassan Joof, Matthew Burton, David Mabey, Dominic Kwiatkowski, Robin Bailey
	Association of a de novo 16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes [My Copy] BMC Medical Genetics, Vol. 10 (16 December 2009), 137. by Tanya Bardakian, Adele Schneider, David Ng, Jennifer Johnston, Leslie Biesecker
	Evidence for an association of HLA-DRB115 and DRB109 with leprosy and the impact of DRB109 on disease onset in a Chinese Han population [My Copy] BMC Medical Genetics*, Vol. 10 (11 December 2009), 133. by Furen Zhang, Hong Liu, Shumin Chen, et al.Changyuan Wang, Chuanfu Zhu, Lin Zhang, Tongsheng Chu, Dianchang Liu, Xiaoxiao Yan, Jianjun Liu
	Association of ADAM33 gene polymorphisms with COPD in a northeastern Chinese population [My Copy] BMC Medical Genetics, Vol. 10 (10 December 2009), 132. by Xinyan Wang, Lei Li, Jinling Xiao, et al.Chengzhen Jin, Kun Huang, Xiaowen Kang, Xiaomei Wu, Fuzhen Lv
	The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924 [My Copy] BMC Medical Genetics, Vol. 10 (09 December 2009), 131. by Josefin Jacobsson, Ulf Riserus, Tomas Axelsson, Lars Lannfelt, Helgi Schioth, Robert Fredriksson
	Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study [My Copy] BMC Medical Genetics, Vol. 10 (09 December 2009), 130. by NanFang Li, HongMei Wang, Jin Yang, et al.Ling Zhou, Jing Hong, YanYing Guo, WenLi Luo, JianHang Chang
	DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort [My Copy] BMC Medical Genetics, Vol. 10 (08 December 2009), 129. by Jose Vazquez-Higuera, Pascual Sanchez-Juan, Eloy Rodriguez-Rodriguez, et al.Ignacio Mateo, Ana Pozueta, Ana Frank, Isabel Sastre, Fernando Valdivieso, Jose Berciano, Maria Bullido, Onofre Combarros
	A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS) [My Copy] BMC Medical Genetics, Vol. 10 (06 December 2009), 128. by Francesc Castro-Giner, Mariona Bustamante, Juan R. Gonzalez, et al.Manolis Kogevinas, Deborah Jarvis, Joachim Heinrich, Josep-Maria Anto, Matthias Wjst, Xavier Estivill, Rafael de Cid
	Power of multifactor dimensionality reduction and penalized logistic regression for detecting gene-gene interaction in a case-control study [My Copy] BMC Medical Genetics, Vol. 10 (04 December 2009), 127. by Hua He, William Oetting, Marcia Brott, Saonli Basu
	The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease [My Copy] BMC Medical Genetics, Vol. 10 (04 December 2009), 126. by Marissa Penna-Martinez, Elizabeth Ramos-Lopez, Inka Robbers, et al.Heinrich Kahles, Stefanie Hahner, Holger Willenberg, Nicole Reisch, Christian Seidl, Maria Segni, Klaus Badenhoop
	Association of vitamin D receptor polymorphisms with the risk of prostate cancer in the Han population of Southern China [My Copy] BMC Medical Genetics, Vol. 10 (04 December 2009), 125. by Yongheng Bai, Yaping Yu, Bin Yu, et al.Jianrong Ge, Jingzhang Ji, Hong Lu, Jia Wei, Zhiliang Weng, Zhihua Tao, Jianxin Lu
	Characterisation of CYP2C8, CYP2C9 and CYP2C19 polymorphisms in a Ghanaian population [My Copy] BMC Medical Genetics, Vol. 10 (02 December 2009), 124. by William Kudzi, Alexander Dodoo, Jeremy Mills
	Analyses of associations between three positionally cloned asthma candidate genes and asthma or asthma-related phenotypes in a Chinese population [My Copy] BMC Medical Genetics, Vol. 10 (01 December 2009), 123. by Huanyu Zhou, Xiumei Hong, Shanqun Jiang, Hongxing Dong, Xiping Xu, Xin Xu
	Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs [My Copy] BMC Medical Genetics, Vol. 10 (01 December 2009), 122. by Elin Blom, Vilmantas Giedraitis, Sampath Arepalli, et al.Marian Hamshere, Omanma Adighibe, Alison Goate, Julie Williams, Lars Lannfelt, John Hardy, Fabienne W. Vrieze, Anna Glaser
	Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (01 December 2009), 121. by Edward Carr, Heather Niederer, Julie Williams, et al.Lorraine Harper, Richard Watts, Paul Lyons, Kenneth Smith
	Relationship of circulating cell-free DNA levels to cell-free fetal DNA levels, clinical characteristics and laboratory parameters in preeclampsia [My Copy] BMC Medical Genetics, Vol. 10 (21 November 2009), 120. by Levente Lazar, Janos Rigo, Balint Nagy, et al.Krisztian Balogh, Veronika Mako, Laszlo Cervenak, Miklos Mezes, Zoltan Prohaszka, Attila Molvarec
	A novel study of Copy Number Variations in Hirschsprung disease using the Multiple Ligation-dependent Probe Amplification (MLPA) technique [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (19 November 2009), 119. by Rocio N. Torres, Raquel Fernandez, Manuel L. Alonso, Guillermo Antinolo, Salud Borrego posted by 1 person jsatkosk
	Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population [My Copy] BMC Medical Genetics, Vol. 10 (18 November 2009), 118. by Chong Shen, Xiangfeng Lu, Yun Li, et al.Qi Zhao, Xiaoli Liu, Liping Hou, Laiyuan Wang, Shufeng Chen, Jianfeng Huang, Dongfeng Gu
	Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma [My Copy] BMC Medical Genetics, Vol. 10 (16 November 2009), 117. by Johanna Schuetz, Amy MacArthur, Stephen Leach, et al.Agnes Lai, Richard Gallagher, Joseph Connors, Randy Gascoyne, John Spinelli, Angela Brooks-Wilson
	Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia [My Copy] BMC Medical Genetics, Vol. 10 (13 November 2009), 116. by Osama Alsmadi, Abdulaziz Al-Ghonaium, Saleh Al-Muhsen, et al.Rand Arnaout, Hasan Al-Dhekri, Bandar Al-Saud, Fadi Al-Kayal, Haya Al-Saud, Hamoud Al-Mousa
	PIN1 gene variants in Alzheimer's disease [My Copy] BMC Medical Genetics, Vol. 10 (12 November 2009), 115. by Aleksandra Maruszak, Krzysztof Safranow, Katarzyna Gustaw, et al.Beata Kijanowska-Haladyna, Katarzyna Jakubowska, Maria Olszewska, Maria Styczynska, Mariusz Berdynski, Andrzej Tysarowski, Dariusz Chlubek, Janusz Siedlecki, Maria Barcikowska, Cezary Zekanowski
	Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation [My Copy] BMC Medical Genetics, Vol. 10 (09 November 2009), 114. by Liu Yuqi, Li Yang, Li Zongbin, et al.Xu Hua, Wen Yi, Wang Lin, Guan Minxin, Gao Lei, Wang Shiwen
	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

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