Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: MCTP2[original query] |
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Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI insight 2022 2 7 (3): . Yu Mengyao, Tcheandjieu Catherine, Georges Adrien, Xiao Ke, Tejeda Helio, Dina Christian, Le Tourneau Thierry, Fiterau Madalina, Judy Renae, Tsao Noah L, Amgalan Dulguun, Munger Chad J, Engreitz Jesse M, Damrauer Scott M, Bouatia-Naji Nabila, Priest James |
Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3. Biological psychiatry 2008 Jun 63 (12): 1185-9. Verma Ranjana, Holmans Peter, Knowles James A, Grover Deepak, Evgrafov Oleg V, Crowe Raymond R, Scheftner William A, Weissman Myrna M, DePaulo J Raymond, Potash James B, Levinson Douglas |
Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE). Psychiatry research 2009 Aug 168 (3): 256-8. Djurovic Srdjan, Le Hellard Stephanie, Kähler Anna K, Jönsson Erik G, Agartz Ingrid, Steen Vidar M, Hall Håkan, Wang August G, Rasmussen Henrik B, Melle Ingrid, Werge Thomas, Andreassen Ole |
New susceptibility loci associated with kidney disease in type 1 diabetes.
PLoS genetics 2012 Sep 8 (9): 9. Sandholm N, Salem RM, McKnight AJ, Brennan EP, Forsblom C, Isakova T, McKay GJ, Williams WW, Sadlier DM, Mäkinen VP, Swan EJ, Palmer C, Boright AP, Ahlqvist E, Deshmukh HA, Keller BJ, Huang H, Ahola AJ, Fagerholm E, Gordin D, Harjutsalo V, He B, Heikkilä O, Hietala K, Kytö J, Lahermo P, Lehto M, Lithovius R, Osterholm AM, Parkkonen M, Pitkäniemi J, Rosengård-Bärlund M, Saraheimo M, Sarti C, Söderlund J, Soro-Paavonen A, Syreeni A, Thorn LM, Tikkanen H, Tolonen N, Tryggvason K, Tuomilehto J, Wadén J, Gill GV, Prior S, Guiducci C, Mirel DB, Taylor A, Hosseini SM, Parving HH, Rossing P, Tarnow L, Ladenvall C, Alhenc-Gelas F, Lefebvre P, Rigalleau V, Roussel R, Tregouet DA, Maestroni A, Maestroni S, Falhammar H, Gu T, Möllsten A, Cimponeriu D, Ioana M, Mota M, Mota E, Serafinceanu C, Stavarachi M, Hanson RL, Nelson RG, Kretzler M, Colhoun HM, Panduru NM, Gu HF, Brismar K, Zerbini G, Hadjadj S, Marre M, Groop L, Lajer M, Bull SB, Waggott D, Paterson AD, Savage DA, Bain SC, Martin F, Hirschhorn JN, Godson C, Florez JC, Groop PH, Maxwell AP |
Replication study for the association of 3 SNP loci identified in a genome-wide association study for diabetic nephropathy in European type 1 diabetes with diabetic nephropathy in Japanese patients with type 2 diabetes. Clinical and experimental nephrology 2013 Dec 17 (6): 866-71. Maeda Shiro, Imamura Minako, Kurashige Mahiro, Araki Shinichi, Suzuki Daisuke, Babazono Tetsuya, Uzu Takashi, Umezono Tomoya, Toyoda Masao, Kawai Koichi, Imanishi Masahito, Hanaoka Kazushige, Maegawa Hiroshi, Uchigata Yasuko, Hosoya Tats |
Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification. Diabetologia 2014 Aug 57 (8): 1611-22. Sambo Francesco, Malovini Alberto, Sandholm Niina, Stavarachi Monica, Forsblom Carol, Mäkinen Ville-Petteri, Harjutsalo Valma, Lithovius Raija, Gordin Daniel, Parkkonen Maija, Saraheimo Markku, Thorn Lena M, Tolonen Nina, Wadén Johan, He Bing, Osterholm Anne-May, Tuomilehto Jaako, Lajer Maria, Salem Rany M, McKnight Amy Jayne, , Tarnow Lise, Panduru Nicolae M, Barbarini Nicola, Di Camillo Barbara, Toffolo Gianna M, Tryggvason Karl, Bellazzi Riccardo, Cobelli Claudio, , Groop Per-Henr |
Systematic search for rare variants in Finnish early-onset colorectal cancer patients. Cancer genetics 0 208 (1-2): 35-40. Tanskanen Tomas, Gylfe Alexandra E, Katainen Riku, Taipale Minna, Renkonen-Sinisalo Laura, Järvinen Heikki, Mecklin Jukka-Pekka, Böhm Jan, Kilpivaara Outi, Pitkänen Esa, Palin Kimmo, Vahteristo Pia, Tuupanen Sari, Aaltonen Lauri |
Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.
Journal of molecular medicine (Berlin, Germany) 2018 Jun . Witten Anika, Bolbrinker Juliane, Barysenka Andrei, Huber Matthias, Rühle Frank, Nowak-Göttl Ulrike, Garbe Edeltraut, Kreutz Reinhold, Stoll Moni |
The Genetic Architecture of Chronic Mountain Sickness in Peru.
Frontiers in genetics 2019 10 690. Gazal Steven, Espinoza Jose R, Austerlitz Frédéric, Marchant Dominique, Macarlupu Jose Luis, Rodriguez Jorge, Ju-Preciado Hugo, Rivera-Chira Maria, Hermine Olivier, Leon-Velarde Fabiola, Villafuerte Francisco C, Richalet Jean-Paul, Gouya Laure |
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 |
Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
A Ferroptosis-Related LncRNA Signature Associated with Prognosis, Tumor Immune Environment, and Genome Instability in Hepatocellular Carcinoma. Computational and mathematical methods in medicine 2022 8 2022 6284540. Lian Jie, Zhang Chaoyu, Lu Hai |
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