Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: NALCN[original query] |
---|
Lack of association of NALCN genetic variants with schizophrenia. Psychiatry research 2011 Feb 185 (3): 450-2. Souza Renan P, Rosa Daniela V F, Romano-Silva Marco A, Zhen Mei, Meltzer Herbert Y, Lieberman Jeffrey A, Remington Gary, Kennedy James L, Wong Albert H |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Schizophrenia research 2010 Dec 124 (1-3): 192-9. Wang Ke-Sheng, Liu Xue-Feng, Aragam Nage |
Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.
Carcinogenesis 2013 Feb 34 (2): 307-13. Lee Youngjoo, Yoon Kyong-Ah, Joo Jungnam, Lee Donghoon, Bae Kieun, Han Ji-Youn, Lee Jin S |
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature 2012 Oct . Biankin AV, Waddell N, Kassahn KS, Gingras MC, Muthuswamy LB, Johns AL, Miller DK, Wilson PJ, Patch AM, Wu J, Chang DK, Cowley MJ, Gardiner BB, Song S, Harliwong I, Idrisoglu S, Nourse C, Nourbakhsh E, Manning S, Wani S, Gongora M, Pajic M, Scarlett CJ, Gill AJ, Pinho AV, Rooman I, Anderson M, Holmes O, Leonard C, Taylor D, Wood S, Xu C, Nones K, Lynn Fink J, Christ A, Bruxner T, Cloonan N, Kolle G, Newell F, Pinese M, Scott Mead R, Humphris JL, Kaplan W, Jones MD, Colvin EK, Nagrial AM, Humphrey ES, Chou A, Chin VT, Chantrill LA, Mawson A, Samra JS, Kench JG, Lovell JA, Daly RJ, Merrett ND, Toon C, Epari K, Nguyen NQ, Barbour A, Zeps N, Biankin AV, Johns AL, Mawson A, Chang DK, Scarlett CJ, Brancato MA, Rowe SJ, Simpson SL, Martyn-Smith M, Thomas MT, Chantrill LA, Chin VT, Chou A, Cowley MJ, Humphris JL, Jones MD, Scott Mead R, Nagrial AM, Pajic M, Pettit J, Pinese M, Rooman I, Wu J, Tao J, Dipietro R, Watson C, Wong R, Pinho AV, Giry-Laterriere M, Daly RJ, Musgrove EA, Sutherland RL, Grimmond SM, Waddell N, Kassahn KS, Miller DK, Wilson PJ, Patch AM, Song S, Harliwong I, Idrisoglu S, Nourse C, Nourbakhsh E, Manning S, Wani S, Gongora M, Anderson M, Holmes O, Leonard C, Taylor D, Wood S, Xu C, Nones K, Lynn Fink J, Christ A, Bruxner T, Cloonan N, Newell F, Pearson JV, Samra JS, Gill AJ, Pavlakis N, Guminski A, Toon C, Biankin AV, Asghari R, Merrett ND, Chang DK, Pavey DA, Das A, Cosman PH, Ismail K, O'Connor C, Lam VW, McLeod D, Pleass HC, Richardson A, James V, Kench JG, Cooper CL, Joseph D, Sandroussi C, Crawford M, Gallagher J, Texler M, Forrest C, Laycock A, Epari KP, Ballal M, Fletcher DR, Mukhedkar S, Spry NA, Deboer B, Chai M, Zeps N, Beilin M, Feeney K, Nguyen NQ, Ruszkiewicz AR, Worthley C, Tan CP, Debrencini T, Chen J, Brooke-Smith ME, Papangelis V, Tang H, Barbour AP, Clouston AD, Martin P, O'Rourke TJ, Chiang A, Fawcett JW, Slater K, Yeung S, Hatzifotis M, Hodgkinson P, Christophi C, Nikfarjam M, Mountain Victorian Cancer Biobank A, Eshleman JR, Hruban RH, Maitra A, Iacobuzio-Donahue CA, Schulick RD, Wolfgang CL, Morgan RA, Hodgin MB, Scarpa A, Lawlor RT, Capelli P, Beghelli S, Corbo V, Scardoni M, Pederzoli P, Tortora G, Bassi C, Tempero MA, Kakkar N, Zhao F, Qing Wu Y, Wang M, Muzny DM, Fisher WE, Charles Brunicardi F, Hodges SE, Reid JG, Drummond J, Chang K, Han Y, Lewis LR, Dinh H, Buhay CJ, Beck T, Timms L, Sam M, Begley K, Brown A, Pai D, Panchal A, Buchner N, De Borja R, Denroche RE, Yung CK, Serra S, Onetto N, Mukhopadhyay D, Tsao MS, Shaw PA, Petersen GM, Gallinger S, Hruban RH, Maitra A, Iacobuzio-Donahue CA, Schulick RD, Wolfgang CL, Morgan RA, Lawlor RT, Capelli P, Corbo V, Scardoni M, Tortora G, Tempero MA, Mann KM, Jenkins NA, Perez-Mancera PA, Adams DJ, Largaespada DA, Wessels LF, Rust AG, Stein LD, Tuveson DA, Copeland NG, Musgrove EA, Scarpa A, Eshleman JR, Hudson TJ, Sutherland RL, Wheeler DA, Pearson JV, McPherson JD, Gibbs RA, Grimmond SM |
Analysis of treatment-resistant schizophrenia and 384 markers from candidate genes. Pharmacogenetics and genomics 2012 Nov 22 (11): 807-11. Teo Celine, Zai Clement, Borlido Carol, Tomasetti Carmine, Strauss John, Shinkai Takahiro, Le Foll Bernard, Wong Albert, Kennedy James L, De Luca Vincen |
Family-based association analysis of alcohol dependence criteria and severity. Alcoholism, clinical and experimental research 2014 Feb 38 (2): 354-66. Wetherill Leah, Kapoor Manav, Agrawal Arpana, Bucholz Kathleen, Koller Daniel, Bertelsen Sarah E, Le Nhung, Wang Jen-Chyong, Almasy Laura, Hesselbrock Victor, Kramer John, Nurnberger John I, Schuckit Marc, Tischfield Jay A, Xuei Xiaoling, Porjesz Bernice, Edenberg Howard J, Goate Alison M, Foroud Tatia |
Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel. Movement disorders : official journal of the Movement Disorder Society 2014 Feb 29 (2): 245-51. Mok Kin Y, Schneider Susanne A, Trabzuni Daniah, Stamelou Maria, Edwards Mark, Kasperaviciute Dalia, Pickering-Brown Stuart, Silverdale Monty, Hardy John, Bhatia Kailash |
Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study. Movement disorders : official journal of the Movement Disorder Society 2014 Dec 29 (14): 1825-8. Gómez-Garre Pilar, Huertas-Fernández Ismael, Cáceres-Redondo María Teresa, Alonso-Canovas Araceli, Bernal-Bernal Inmaculada, Blanco-Ollero Alberto, Bonilla-Toribio Marta, Burguera Juan Andrés, Carballo Manuel, Carrillo Fatima, José Catalán-Alonso M, Escamilla-Sevilla Francisco, Espinosa-Rosso Raul, Carmen Fernández-Moreno María, García-Caldentey Juan, García-Moreno José Manuel, Giacometti-Silveira Sandra, Gutiérrez-García Javier, Jesús-Maestre Silvia, López-Valdés Eva, Martínez-Castrillo Juan Carlos, Medialdea-Natera María Pilar, Méndez-Lucena Carolina, Mínguez-Castellanos Adolfo, Angel Moya Miguel, Ochoa-Sepulveda Juan José, Ojea Tomas, Rodríguez Nuria, Rubio-Agusti Ignacio, Sillero-Sánchez Miriam, Del Val Javier, Vargas-González Laura, Mir Pab |
Association Analysis of NALCN Polymorphisms rs1338041 and rs61973742 in a Chinese Population with Isolated Cervical Dystonia. Parkinson's disease 2016 2016 9281790. Zhou Qingqing, Yang Jing, Cao Bei, Chen Yongping, Wei Qianqian, Ou Ruwei, Song Wei, Zhao Bi, Wu Ying, Shang Huifa |
Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort. Acta medica Lituanica 2018 25 (1): 7-13. Baronas Karolis, Ran?elis Tautvydas, Pranculis Aidas, Domarkien? Ingrida, Ambrozaityt? Laima, Ku?inskas Vaidut |
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.
Soa--ch'ongsonyon chongsin uihak = Journal of child & adolescent psychiatry 2018 Apr 29 (2): 62-72. Kweon Kukju, Shin Eun-Soon, Park Kee Jeong, Lee Jong-Keuk, Joo Yeonho, Kim Hyo-W |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. medRxiv : the preprint server for health sciences 2020 Nov . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Identification of Genetic Susceptibility Factors Associated with Canine Gastric Dilatation-Volvulus. Genes 2020 Nov 11 (11): . Piras Ignazio S, Perdigones Nieves, Zismann Victoria, Briones Natalia, Facista Salvatore, Rivera José Luis, Rozanski Elizabeth, London Cheryl A, Hendricks William P |
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS genetics 2021 Jul 17 (7): e1009679. Audain Enrique, Wilsdon Anna, Breckpot Jeroen, Izarzugaza Jose M G, Fitzgerald Tomas W, Kahlert Anne-Karin, Sifrim Alejandro, Wünnemann Florian, Perez-Riverol Yasset, Abdul-Khaliq Hashim, Bak Mads, Bassett Anne S, Benson D Woodrow, Berger Felix, Daehnert Ingo, Devriendt Koenraad, Dittrich Sven, Daubeney Piers Ef, Garg Vidu, Hackmann Karl, Hoff Kirstin, Hofmann Philipp, Dombrowsky Gregor, Pickardt Thomas, Bauer Ulrike, Keavney Bernard D, Klaassen Sabine, Kramer Hans-Heiner, Marshall Christian R, Milewicz Dianna M, Lemaire Scott, Coselli Joseph S, Mitchell Michael E, Tomita-Mitchell Aoy, Prakash Siddharth K, Stamm Karl, Stewart Alexandre F R, Silversides Candice K, Siebert Reiner, Stiller Brigitte, Rosenfeld Jill A, Vater Inga, Postma Alex V, Caliebe Almuth, Brook J David, Andelfinger Gregor, Hurles Matthew E, Thienpont Bernard, Larsen Lars Allan, Hitz Marc-Phill |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 Apr . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, , Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Association Between Dystonia-Related Genetic Loci and Parkinson's Disease in Eastern China. Frontiers in neurology 2022 3 12 711050. Yang Wen-Yi, Jiang Si-Si, Pu Jia-Li, Jin Chong-Yao, Gao Ting, Zheng Ran, Tian Jun, Zhang Bao-Ro |
Novel NALCN variant linked to temporal lobe epilepsy. American journal of medical genetics. Part A 2023 4 . Nguyen Emmanuelle, Tétreault Martine, Toffa Dènahin Hinnoutondji, Cossette Patrick, Samarut Éric, Nguyen Dang Kh |
Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis. Human genomics 2023 10 17 (1): 88. Susanna Nousiainen, Outi Kuismin, Siiri Reinikka, Roosa Manninen, Sara Khamaiseh, Mari Kuivalainen, Anna Terho, Sari Koivurova, Maarit Niinimäki, Kari Salokas, Markku Varjosalo, Anne Ahtikoski, Ralf Bützow, Outi Lindgren, Outi Uimari, Pia Vahteris |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: