Human Genome Epidemiology Literature Finder
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CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jan 116B (1): 45-50. Laurent Claudine, Niehaus Dana, Bauché Stéphanie, Levinson Douglas F, Soubigou Stéphane, Pimstone Simon, Hayden Michael, Mbanga Irena, Emsley Robin, Deleuze Jean-François, Mallet Jacqu |
Lack of association of matrix metalloproteinase 3 (MMP3) genotypes with ankylosing spondylitis susceptibility and severity. Rheumatology (Oxford, England) 2005 Jan 44 (1): 55-60. Jin L, Weisman M, Zhang G, Ward M, Luo J, Bruckel J, Inman R, Khan M A, Schumacher H R, Maksymowych W P, Mahowald M, Martin T, Rosenbaum J T, Yu D T Y, Stone M, Watson J, Dickman E, Davis J, Reveille J |
Lipoprotein lipase gene is linked and associated with hypertension in Taiwan young-onset hypertension genetic study. Journal of biomedical science 2005 12 (4): 651-8. Chen P, Jou YS, Fann CS, Chen JW, Wu SY, Pan WH |
Fine mapping of a region on chromosome 21q21.11-q22.3 showing linkage to type 1 diabetes. Journal of medical genetics 2005 1 42 (1): 17-25. Bergholdt R, Nerup J, Pociot |
Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23. The British journal of dermatology 2005 1 152 (1): 29-36. Lin M-W, Lee D-D, Lin C-H, Huang C-Y, Wong C-K, Chang Y-T, Liu H-N, Hsiao K-J, Tsai S |
Linkage analysis of chromosome 1 with essential hypertension and blood pressure quantitative traits in Chinese families. Annals of human genetics 2005 1 69 (Pt 1): 45-54. Ge D, Huang J, Yang W, Zhao J, Shen Y, Qiang B, Gu |
Significant linkage and association between a functional (GT)n polymorphism in promoter of the N-methyl-D-aspartate receptor subunit gene (GRIN2A) and schizophrenia. Neuroscience letters 2006 Nov 409 (1): 80-2. Tang Jinsong, Chen Xiaogang, Xu Xijia, Wu Renrong, Zhao Jingping, Hu Zhengmao, Xia K |
Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree. Human heredity 2006 1 60 (4): 220-6. Coon Hilary, Matsunami Nori, Stevens Jeff, Miller Judith, Pingree Carmen, Camp Nicola J, Thomas Alun, Krasny Lori, Lainhart Janet, Leppert Mark F, McMahon Willi |
Evidence for linkage and association between autoimmune thyroid diseases and the 18q12-q21 region in a large Tunisian family. International journal of immunogenetics 2006 1 33 (1): 25-32. Hadj Kacem H, Rebai A, Kaffel N, Abid M, Ayadi |
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population. European journal of human genetics : EJHG 2008 Jan 16 (1): 105-14. Engert James C, Lemire Mathieu, Faith Janet, Brisson Diane, Fujiwara T Mary, Roslin Nicole M, Brewer Carl G, Montpetit Alexandre, Darmond-Zwaig Corinne, Renaud Yannick, Doré Carole, Bailey Swneke D, Verner Andrei, Tremblay Gérald, St-Pierre Julie, Bétard Christine, Platko Jill, Rioux John D, Morgan Kenneth, Hudson Thomas J, Gaudet Dani |
Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol. Hepatology (Baltimore, Md.) 2007 Sep 46 (3): 793-801. Grünhage Frank, Acalovschi Monica, Tirziu Simona, Walier Maja, Wienker Thomas F, Ciocan Anca, Mosteanu Ofelia, Sauerbruch Tilman, Lammert Fra |
Candidate gene analysis of 21q22: support for S100B as a susceptibility gene for bipolar affective disorder with psychosis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Dec 144B (8): 1094-6. Roche S, Cassidy F, Zhao C, Badger J, Claffey E, Mooney L, Delaney C, Dobrin S, McKeon |
Evaluating the association of common PBX1 variants with type 2 diabetes. BMC medical genetics 2008 9 (1): 14. Duesing Konsta, Charpentier Guillaume, Marre Michel, Tichet Jean, Hercberg Serge, Balkau Beverley, Froguel Philippe, Gibson Fernan |
An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1152-8. Ramoz Nicolas, Cai Guiqing, Reichert Jennifer G, Silverman Jeremy M, Buxbaum Joseph |
Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping. Human genetics 2009 Dec 126 (6): 805-17. McDonough Caitrin W, Bostrom Meredith A, Lu Lingyi, Hicks Pamela J, Langefeld Carl D, Divers Jasmin, Mychaleckyj Josyf C, Freedman Barry I, Bowden Donald |
Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Dec 18 (12): 3399-406. Hardin Jill, He Yungang, Javitz Harold S, Wessel Jennifer, Krasnow Ruth E, Tildesley Elizabeth, Hops Hyman, Swan Gary E, Bergen Andrew |
Analysis of the common vasoactive intestinal peptide receptor 1 polymorphism in gallstone patients. Journal of gastrointestinal and liver diseases : JGLD 2010 Sep 19 (3): 273-7. Krawczyk Marcin, Rusticeanu Monica, Grünhage Frank, Mahler Miriam, Portincasa Piero, Acalovschi Monica, Lammert Fra |
The common adiponutrin variant p.I148M does not confer gallstone risk but affects fasting glucose and triglyceride levels. Journal of physiology and pharmacology : an official journal of the Polish Physiological Society 2011 Jun 62 (3): 369-75. Krawczyk M, Gruenhage F, Mahler M, Tirziu S, Acalovschi M, Lammert |
Bipolar disorder susceptibility region on chromosome 3q29 not confirmed in a case-control association study. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2011 Jun 12 (4): 309-15. Schosser Alexandra, Schloegelhofer Monika, Fuchs Karoline, Stojanovic Mirjana, Mossaheb Nilufar, Kindler Jochen, Cohen-Woods Sarah, Hosang Georgina, Farmer Anne, Craig Ian, McGuffin Peter, Aschauer Hara |
Association of a single nucleotide polymorphism in pregnancy-associated plasma protein-A2 with developmental dysplasia of the hip: a case-control study. Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2012 Jan 20 (1): 60-3. Jia Jingyu, Li Lianyong, Zhao Qun, Zhang Lijun, Ru Jiling, Liu Xijuan, Li Qiwi, Shi Liw |
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. European journal of human genetics : EJHG 2011 1 19 (6): 687-95. Villanueva Pia, Newbury Dianne F, Jara Lilian, De Barbieri Zulema, Mirza Ghazala, Palomino Hernán M, Fernández María Angélica, Cazier Jean-Baptiste, Monaco Anthony P, Palomino Hern |
A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families. European journal of human genetics : EJHG 2012 Sep 20 (9): 965-72. Kruse Lisbeth Venø, Nyegaard Mette, Christensen Ulla, Møller-Larsen Steffen, Haagerup Annette, Deleuran Mette, Hansen Lars Gudmund, Venø Stine Krogh, Goossens Dirk, Del-Favero Jurgen, Børglum Anders Dupo |
Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families. PloS one 2014 9 (12): e113935. Gao Hanxiang, Li Lin, Rao Shaoqi, Shen Gongqing, Xi Quansheng, Chen Shenghan, Zhang Zheng, Wang Kai, Ellis Stephen G, Chen Qiuyun, Topol Eric J, Wang Qing |
Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia. Molecular neuropsychiatry 2015 May 1 (1): 36-46. Zeledón Mariela, Eckart Nicole, Taub Margaret, Vernon Hilary, Szymanksi Megan, Wang Ruihua, Chen Pei-Lung, Nestadt Gerry, McGrath John A, Sawa Akira, Pulver Ann E, Avramopoulos Dimitrios, Valle Dav |
Role of Deleterious Rare Alleles for Acute-Onset Diffuse Interstitial Lung Disease in Collagen Diseases. Clinical medicine insights. Circulatory, respiratory and pulmonary medicine 2019 13 1179548419866443. Furukawa Hiroshi, Oka Shomi, Shimada Kota, Hashimoto Atsushi, Komiya Akiko, Matsui Toshihiro, Tohma Shige |
Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves' Disease in the Chinese Han Population. Medical science monitor : international medical journal of experimental and clinical research 2019 Feb 25 1439-1451. Li Jia, Teng Weiping, Yu Yang, Hou Xin, Shan Zhongy |
A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data. American journal of human genetics 2019 10 105 (4): 822-835. Zhao Linhai, He Zongxiao, Zhang Di, Wang Gao T, Renton Alan E, Vardarajan Badri N, Nothnagel Michael, Goate Alison M, Mayeux Richard, Leal Suzanne |
RASAL1 and ROS1 Gene Variants in Hereditary Breast Cancer. Cancers 2020 Sep 12 (9): . Isidori Federica, Bozzarelli Isotta, Ferrari Simona, Godino Lea, Innella Giovanni, Turchetti Daniela, Bonora Ele |
Mapping of developmental dysplasia of the hip to two novel regions at 8q23-q24 and 12p12. Experimental and therapeutic medicine 2020 4 19 (4): 2799-2803. Zhang Lixin, Xu Xiaowen, Chen Yufan, Li Lianyong, Zhang Lijun, Li Qiw |
Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
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- Page last updated:May 13, 2024
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