Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: NTN4[original query] |
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Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
Carcinogenesis 2014 May 35 (5): 1012-9. Purrington Kristen S, Slager Susan, Eccles Diana, Yannoukakos Drakoulis, Fasching Peter A, Miron Penelope, Carpenter Jane, Chang-Claude Jenny, Martin Nicholas G, Montgomery Grant W, Kristensen Vessela, Anton-Culver Hoda, Goodfellow Paul, Tapper William J, Rafiq Sajjad, Gerty Susan M, Durcan Lorraine, Konstantopoulou Irene, Fostira Florentia, Vratimos Athanassios, Apostolou Paraskevi, Konstanta Irene, Kotoula Vassiliki, Lakis Sotiris, Dimopoulos Meletios A, Skarlos Dimosthenis, Pectasides Dimitrios, Fountzilas George, Beckmann Matthias W, Hein Alexander, Ruebner Matthias, Ekici Arif B, Hartmann Arndt, Schulz-Wendtland Ruediger, Renner Stefan P, Janni Wolfgang, Rack Brigitte, Scholz Christoph, Neugebauer Julia, Andergassen Ulrich, Lux Michael P, Haeberle Lothar, Clarke Christine, Pathmanathan Nirmala, Rudolph Anja, Flesch-Janys Dieter, Nickels Stefan, Olson Janet E, Ingle James N, Olswold Curtis, Slettedahl Seth, Eckel-Passow Jeanette E, Anderson S Keith, Visscher Daniel W, Cafourek Victoria L, Sicotte Hugues, Prodduturi Naresh, Weiderpass Elisabete, Bernstein Leslie, Ziogas Argyrios, Ivanovich Jennifer, Giles Graham G, Baglietto Laura, Southey Melissa, Kosma Veli-Matti, Fischer Hans-Peter, , Reed Malcom W R, Cross Simon S, Deming-Halverson Sandra, Shrubsole Martha, Cai Qiuyin, Shu Xiao-Ou, Daly Mary, Weaver Joellen, Ross Eric, Klemp Jennifer, Sharma Priyanka, Torres Diana, Rüdiger Thomas, Wölfing Heidrun, Ulmer Hans-Ulrich, Försti Asta, Khoury Thaer, Kumar Shicha, Pilarski Robert, Shapiro Charles L, Greco Dario, Heikkilä Päivi, Aittomäki Kristiina, Blomqvist Carl, Irwanto Astrid, Liu Jianjun, Pankratz Vernon Shane, Wang Xianshu, Severi Gianluca, Mannermaa Arto, Easton Douglas, Hall Per, Brauch Hiltrud, Cox Angela, Zheng Wei, Godwin Andrew K, Hamann Ute, Ambrosone Christine, Toland Amanda Ewart, Nevanlinna Heli, Vachon Celine M, Couch Fergus |
Genetic association signal near NTN4 in Tourette syndrome. Annals of neurology 2014 Aug 76 (2): 310-5. Paschou Peristera, Yu Dongmei, Gerber Gloria, Evans Patrick, Tsetsos Fotis, Davis Lea K, Karagiannidis Iordanis, Chaponis Jonathan, Gamazon Eric, Mueller-Vahl Kirsten, Stuhrmann Manfred, Schloegelhofer Monika, Stamenkovic Mara, Hebebrand Johannes, Noethen Markus, Nagy Peter, Barta Csaba, Tarnok Zsanett, Rizzo Renata, Depienne Christel, Worbe Yulia, Hartmann Andreas, Cath Danielle C, Budman Cathy L, Sandor Paul, Barr Cathy, Wolanczyk Thomas, Singer Harvey, Chou I-Ching, Grados Marco, Posthuma Danielle, Rouleau Guy A, Aschauer Harald, Freimer Nelson B, Pauls David L, Cox Nancy J, Mathews Carol A, Scharf Jeremiah |
Volumetric mammographic density: heritability and association with breast cancer susceptibility loci. Journal of the National Cancer Institute 2014 Dec 106 (12): . Brand Judith S, Humphreys Keith, Thompson Deborah J, Li Jingmei, Eriksson Mikael, Hall Per, Czene Kami |
Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Genes, brain, and behavior 2015 Sep . Saad M, Brkanac Z, Wijsman E |
Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures. Cancer research 2015 Jun 75 (12): 2457-67. Stone Jennifer, Thompson Deborah J, Dos Santos Silva Isabel, Scott Christopher, Tamimi Rulla M, Lindstrom Sara, Kraft Peter, Hazra Aditi, Li Jingmei, Eriksson Louise, Czene Kamila, Hall Per, Jensen Matt, Cunningham Julie, Olson Janet E, Purrington Kristen, Couch Fergus J, Brown Judith, Leyland Jean, Warren Ruth M L, Luben Robert N, Khaw Kay-Tee, Smith Paula, Wareham Nicholas J, Jud Sebastian M, Heusinger Katharina, Beckmann Matthias W, Douglas Julie A, Shah Kaanan P, Chan Heang-Ping, Helvie Mark A, Le Marchand Loic, Kolonel Laurence N, Woolcott Christy, Maskarinec Gertraud, Haiman Christopher, Giles Graham G, Baglietto Laura, Krishnan Kavitha, Southey Melissa C, Apicella Carmel, Andrulis Irene L, Knight Julia A, Ursin Giske, Alnaes Grethe I Grenaker, Kristensen Vessela N, Borresen-Dale Anne-Lise, Gram Inger Torhild, Bolla Manjeet K, Wang Qin, Michailidou Kyriaki, Dennis Joe, Simard Jacques, Pharoah Paul, Dunning Alison M, Easton Douglas F, Fasching Peter A, Pankratz V Shane, Hopper John L, Vachon Celine |
Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in neuroscience 2016 10 531. Padmanabhuni Shanmukha S, Houssari Rayan, Esserlind Ann-Louise, Olesen Jes, Werge Thomas M, Hansen Thomas F, Bertelsen Birgitte, Tsetsos Fotis, Paschou Peristera, Tümer Zeyn |
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease. Journal of medical genetics 2019 9 57 (2): 82-88. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, May Patrick, Lopez-Escamez Jose |
3'UTR variants of TNS3, PHLDB1, NTN4, and GNG2 genes are associated with IgA nephropathy risk in Chinese Han population. International immunopharmacology 2019 Mar 71 295-300. Feng Yuan, Su Yan, Ma Chunyang, Jing Ziyang, Yang Xiaohong, Zhang Daofa, Xie Maowei, Li Wenning, Wei Jia |
Genome-wide association meta-analysis of functional outcome after ischemic stroke.
Neurology 2019 Mar 92 (12): e1271-e1283. Söderholm Martin, Pedersen Annie, Lorentzen Erik, Stanne Tara M, Bevan Steve, Olsson Maja, Cole John W, Fernandez-Cadenas Israel, Hankey Graeme J, Jimenez-Conde Jordi, Jood Katarina, Lee Jin-Moo, Lemmens Robin, Levi Christopher, Mitchell Braxton D, Norrving Bo, Rannikmäe Kristiina, Rost Natalia S, Rosand Jonathan, Rothwell Peter M, Scott Rodney, Strbian Daniel, Sturm Jonathan W, Sudlow Cathie, Traylor Matthew, Thijs Vincent, Tatlisumak Turgut, Woo Daniel, Worrall Bradford B, Maguire Jane M, Lindgren Arne, Jern Christina, |
Genome-Wide Association Analysis of Single-Breath Dl.
American journal of respiratory cell and molecular biology 2019 Jan . Sakornsakolpat Phuwanat, McCormack Meredith, Bakke Per, Gulsvik Amund, Make Barry J, Crapo James D, Cho Michael H, Silverman Edwin |
eQTL Colocalization Analyses Identify NTN4 as a Candidate Breast Cancer Risk Gene. American journal of human genetics 2020 9 107 (4): 778-787. Beesley Jonathan, Sivakumaran Haran, Moradi Marjaneh Mahdi, Shi Wei, Hillman Kristine M, Kaufmann Susanne, Hussein Nehal, Kar Siddhartha, Lima Luize G, Ham Sunyoung, Möller Andreas, Chenevix-Trench Georgia, Edwards Stacey L, French Juliet |
Germline Mutations in Familial Papillary Thyroid Cancer. Endocrine pathology 2020 Feb . Sarquis Marta, Moraes Debora C, Bastos-Rodrigues Luciana, Azevedo Pedro G, Ramos Adauto V, Reis Fabiana Versiani, Dande Paula V, Paim Isabela, Friedman Eitan, De Marco Lu |
The Interaction of NTN4 and miR-17-92 Polymorphisms on Breast Cancer Susceptibility in a Chinese Population. Clinical breast cancer 2021 Dec . Wang Yi-Shan, Guo Rong, Yang De-Chun, Xu Yi, Hui Ying-Xiang, Li Dan-Dan, Tang Shi-Cong, Tang Yi-Y |
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- Page last updated:Apr 22, 2024
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