Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: NSF[original query] |
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Novel haplotypes in 17q21 are associated with progressive supranuclear palsy. Annals of neurology 2004 Aug 56 (2): 249-58. Pastor Pau, Ezquerra Mario, Perez J Christian, Chakraverty Sumi, Norton Joanne, Racette Brad A, McKeel Dan, Perlmutter Joel S, Tolosa Eduardo, Goate Alison |
Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder. Psychiatric genetics 2006 Feb 16 (1): 3-8. Weller Andrew E, Dahl John P, Lohoff Falk W, Ferraro Thomas N, Berrettini Wade |
Associations between renal sodium-citrate cotransporter (hNaDC-1) gene polymorphism and urinary citrate excretion in recurrent renal calcium stone formers and normal controls. International journal of urology : official journal of the Japanese Urological Association 2007 Apr 14 (4): 344-9. Okamoto Naohiko, Aruga Seiji, Matsuzaki Shoji, Takahashi Satoru, Matsushita Kazuo, Kitamura Tadaic |
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2007 Dec 104 (50): 19942-7. Lencz Todd, Lambert Christophe, DeRosse Pamela, Burdick Katherine E, Morgan T Vance, Kane John M, Kucherlapati Raju, Malhotra Anil |
Associations of SNAP-25 polymorphisms with cognitive dysfunctions in Caucasian patients with schizophrenia during a brief trail of treatment with atypical antipsychotics. European archives of psychiatry and clinical neuroscience 2008 Sep 258 (6): 335-44. Spellmann Ilja, Müller Norbert, Musil Richard, Zill Peter, Douhet Anette, Dehning Sandra, Cerovecki Anja, Bondy Brigitta, Möller Hans-Jürgen, Riedel Micha |
No evidence for excess runs of homozygosity in bipolar disorder. Psychiatric genetics 2009 Aug 19 (4): 165-70. Vine Anna E, McQuillin Andrew, Bass Nicholas J, Pereira Ana, Kandaswamy Radhika, Robinson Michele, Lawrence Jacob, Anjorin Adebayo, Sklar Pamela, Gurling Hugh M D, Curtis Dav |
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
Candidate pathway association study in cocaine dependence: the control of neurotransmitter release. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012 Feb 13 (2): 126-34. Fernàndez-Castillo Noèlia, Cormand Bru, Roncero Carlos, Sánchez-Mora Cristina, Grau-Lopez Lara, Gonzalvo Begoña, Miquel Laia, Corominas Roser, Ramos-Quiroga Josep Antoni, Casas Miquel, Ribasés Mar |
Fibrosis-associated single-nucleotide polymorphisms in TGFB1 and CAV1 are not associated with the development of nephrogenic systemic fibrosis. The American Journal of dermatopathology 2013 May 35 (3): 351-6. Le Long P, Garibyan Lilit, Lara Daniel, Finberg Karin E, Iafrate A John, Duncan Lyn M, Kay Jonathan, Nazarian Rosalynn |
Genomic copy number variants: evidence for association with antibody response to anthrax vaccine adsorbed. PloS one 2013 8 (5): e64813. Falola Michael I, Wiener Howard W, Wineinger Nathan E, Cutter Gary R, Kimberly Robert P, Edberg Jeffrey C, Arnett Donna K, Kaslow Richard A, Tang Jianming, Shrestha Sade |
Crohn's disease loci are common targets of protozoa-driven selection. Molecular biology and evolution 2013 May 30 (5): 1077-87. Cagliani Rachele, Pozzoli Uberto, Forni Diego, Cassinotti Andrea, Fumagalli Matteo, Giani Matteo, Fichera Maria, Lombardini Marta, Ardizzone Sandro, Asselta Rosanna, de Franchis Roberto, Riva Stefania, Biasin Mara, Comi Giacomo P, Bresolin Nereo, Clerici Mario, Sironi Manue |
Coeliac disease-associated polymorphisms influence thymic gene expression. Genes and immunity 2014 Sep 15 (6): 355-60. Amundsen S S, Viken M K, Sollid L M, Lie B |
The schizophrenia risk gene product miR-137 alters presynaptic plasticity. Nature neuroscience 2015 Jul 18 (7): 1008-16. Siegert Sandra, Seo Jinsoo, Kwon Ester J, Rudenko Andrii, Cho Sukhee, Wang Wenyuan, Flood Zachary, Martorell Anthony J, Ericsson Maria, Mungenast Alison E, Tsai Li-Hu |
Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.
Medicine 2015 Nov 94 (47): e1892. Dong Jing, Yang Jingyun, Tranah Greg, Franceschini Nora, Parimi Neeta, Alkorta-Aranburu Gorka, Xu Zongli, Alonso Alvaro, Cummings Steven R, Fornage Myriam, Huang Xuemei, Kritchevsky Stephen, Liu Yongmei, London Stephanie, Niu Liang, Wilson Robert S, De Jager Philip L, Yu Lei, Singleton Andrew B, Harris Tamara, Mosley Thomas H, Pinto Jayant M, Bennett David A, Chen Hongl |
A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence. Scientific reports 2016 08 6 31033. Cabana-Domínguez Judit, Roncero Carlos, Grau-López Lara, Rodríguez-Cintas Laia, Barral Carmen, Abad Alfonso C, Erikson Galina, Wineinger Nathan E, Torrico Bàrbara, Arenas Concepció, Casas Miquel, Ribasés Marta, Cormand Bru, Fernàndez-Castillo Noèl |
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia. Acta neuropathologica 2017 05 133 (5): 825-837. Yokoyama Jennifer S, Karch Celeste M, Fan Chun C, Bonham Luke W, Kouri Naomi, Ross Owen A, Rademakers Rosa, Kim Jungsu, Wang Yunpeng, Höglinger Günter U, Müller Ulrich, Ferrari Raffaele, Hardy John, , Momeni Parastoo, Sugrue Leo P, Hess Christopher P, James Barkovich A, Boxer Adam L, Seeley William W, Rabinovici Gil D, Rosen Howard J, Miller Bruce L, Schmansky Nicholas J, Fischl Bruce, Hyman Bradley T, Dickson Dennis W, Schellenberg Gerard D, Andreassen Ole A, Dale Anders M, Desikan Rahul |
Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells. Arteriosclerosis, thrombosis, and vascular biology 2018 Jun . Schillemans Maaike, Karampini Ellie, van den Eshof Bart, Gangaev Anastasia, Hofman Menno, van Breevoort Dorothee, Meems Henriët, Janssen Hans, Mulder Aat A, Jost Carolina R, Escher Johanna C, Adam Rüdiger, Carter Tom, Koster Abraham J, van den Biggelaar Maartje, Voorberg Jan, Bierings Rub |
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. JAMA neurology 2018 Jul 75 (7): 860-875. Karch Celeste M, Wen Natalie, Fan Chun C, Yokoyama Jennifer S, Kouri Naomi, Ross Owen A, Höglinger Gunter, Müller Ulrich, Ferrari Raffaele, Hardy John, Schellenberg Gerard D, Sleiman Patrick M, Momeni Parastoo, Hess Christopher P, Miller Bruce L, Sharma Manu, Van Deerlin Vivianna, Smeland Olav B, Andreassen Ole A, Dale Anders M, Desikan Rahul S, |
Interaction networks of Weibel-Palade body regulators syntaxin-3 and syntaxin binding protein 5 in endothelial cells. Journal of proteomics 2019 6 205 103417. Schillemans Maaike, Karampini Ellie, Hoogendijk Arie J, Wahedi Maryam, van Alphen Floris P J, van den Biggelaar Maartje, Voorberg Jan, Bierings Rub |
A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.
Behavior genetics 2019 Jan . Arias-Vásquez A, Groffen A J, Spijker S, Ouwens K G, Klein M, Vojinovic D, Galesloot T E, Bralten J, Hottenga J J, van der Most P J, Kattenberg V M, Pool R, Nolte I M, Penninx B W J H, Fedko I O, Dolan C V, Nivard M G, den Braber A, van Duijn C M, Hoekstra P J, Buitelaar J K, Kiemeney L A, Hoogman M, Middeldorp C M, Draisma H H M, Vermeulen S H, Sánchez-Mora C, Ramos-Quiroga J A, Ribasés M, , Hartman C A, Kooij J J S, Amin N, Smit A B, Franke B, Boomsma D |
Identifying Risk Genes and Interpreting Pathogenesis for Parkinson's Disease by a Multiomics Analysis. Genes 2020 9 11 (9): . Cheng Wen-Wen, Zhu Qiang, Zhang Hong- |
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease. Parkinsonism & related disorders 2020 Aug 78 138-144. Soto-Beasley Alexandra I, Walton Ronald L, Valentino Rebecca R, Hook Paul W, Labbé Catherine, Heckman Michael G, Johnson Patrick W, Goff Loyal A, Uitti Ryan J, McLean Pamela J, Springer Wolfdieter, McCallion Andrew S, Wszolek Zbigniew K, Ross Owen |
Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers. Journal of Alzheimer's disease : JAD 2020 Jul . Fan Kang-Hsien, Feingold Eleanor, Rosenthal Samantha L, Demirci F Yesim, Ganguli Mary, Lopez Oscar L, Kamboh M Ily |
Multimodal analysis of gene expression from postmortem brains and blood identifies synaptic vesicle trafficking genes to be associated with Parkinson's disease. Briefings in bioinformatics 2020 10 22 (4): . Gao Xiaoya, Huang Zifeng, Feng Cailing, Guan Chaohao, Li Ruidong, Xie Haiting, Chen Jian, Li Mingchun, Que Rongfang, Deng Bin, Cao Peihua, Li Mengyan, Lu Jianjun, Huang Yihong, Li Minzi, Yang Weihong, Yang Xiaohua, Wen Chunyan, Liang Xiaomei, Yang Qin, Chao Yin-Xia, Chan Ling-Ling, Yenari Midori A, Jin Kunlin, Chaudhuri K Ray, Zhang Jing, Tan Eng-King, Wang Qi |
Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy. Epileptic disorders : international epilepsy journal with videotape 2021 Jul . Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji |
NAPB and developmental and epileptic encephalopathy: description of the electro-clinical profile associated to a novel pathogenic variant. Epilepsia 2023 4 . Mignon-Ravix Cécile, Riccardi Florence, Daquin Géraldine, Cacciagli Pierre, Lamoureux-Toth Sylvie, Villard Laurent, Villeneuve Nathalie, Molinari Floren |
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. Movement disorders : official journal of the Movement Disorder Society 2023 2 . Sugier Pierre-Emmanuel, Lucotte Elise A, Domenighetti Cloé, Law Matthew H, Iles Mark M, Brown Kevin, Amos Christopher, McKay James D, Hung Rayjean J, Karimi Mojgan, Bacq-Daian Delphine, Boland-Augé Anne, Olaso Robert, Deleuze Jean-François, Lesueur Fabienne, Ostroumova Evgenia, Kesminiene Ausrele, de Vathaire Florent, Guénel Pascal, , Sreelatha Ashwin Ashok Kumar, Schulte Claudia, Grover Sandeep, May Patrick, Bobbili Dheeraj R, Radivojkov-Blagojevic Milena, Lichtner Peter, Singleton Andrew B, Hernandez Dena G, Edsall Connor, Mellick George D, Zimprich Alexander, Pirker Walter, Rogaeva Ekaterina, Lang Anthony E, Koks Sulev, Taba Pille, Lesage Suzanne, Brice Alexis, Corvol Jean-Christophe, Chartier-Harlin Marie-Christine, Mutez Eugénie, Brockmann Kathrin, Deutschländer Angela B, Hadjigeorgiou Georges M, Dardiotis Efthimios, Stefanis Leonidas, Simitsi Athina Maria, Valente Enza Maria, Petrucci Simona, Straniero Letizia, Zecchinelli Anna, Pezzoli Gianni, Brighina Laura, Ferrarese Carlo, Annesi Grazia, Quattrone Andrea, Gagliardi Monica, Matsuo Hirotaka, Nakayama Akiyoshi, Hattori Nobutaka, Nishioka Kenya, Chung Sun Ju, Kim Yun Joong, Kolber Pierre, van de Warrenburg Bart P C, Bloem Bastiaan R, Aasly Jan, Toft Mathias, Pihlstrøm Lasse, Guedes Leonor Correia, Ferreira Joaquim J, Bardien Soraya, Carr Jonathan, Tolosa Eduardo, Ezquerra Mario, Pastor Pau, Diez-Fairen Monica, Wirdefeldt Karin, Pedersen Nancy, Ran Caroline, Belin Andrea C, Puschmann Andreas, Rödström Emil Ygland, Clarke Carl E, Morrison Karen E, Tan Manuela, Krainc Dimitri, Burbulla Lena F, Farrer Matt J, Kruger Rejko, Gasser Thomas, Sharma Manu, , Truong Thérèse, Elbaz Alex |
Epidemiologic association and shared genetic architecture between cataract and hearing difficulties among middle-aged and older adults. Human genomics 2024 4 18 (1): 39. Xiayin Zhang, Shan Wang, Shunming Liu, Zijing Du, Guanrong Wu, Yingying Liang, Yu Huang, Xianwen Shang, Yijun Hu, Zhuoting Zhu, Wei Sun, Xueli Zhang, Honghua |
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- Page last updated:Apr 22, 2024
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