Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: SEMA3A[original query] |
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Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families. Molecular psychiatry 2008 Jul 13 (7): 673-84. Wedenoja J, Loukola A, Tuulio-Henriksson A, Paunio T, Ekelund J, Silander K, Varilo T, Heikkilä K, Suvisaari J, Partonen T, Lönnqvist J, Peltonen |
Candidate gene analysis of semaphorins in patients with Alzheimer's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2010 Apr 31 (2): 169-73. Villa Chiara, Venturelli Eliana, Fenoglio Chiara, De Riz Milena, Scalabrini Diego, Cortini Francesca, Serpente Maria, Cantoni Claudia, Bresolin Nereo, Scarpini Elio, Galimberti Danie |
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.
American journal of human genetics 2011 Aug 89 (2): 334-43. Larsson Mats, Duffy David L, Zhu Gu, Liu Jimmy Z, Macgregor Stuart, McRae Allan F, Wright Margaret J, Sturm Richard A, Mackey David A, Montgomery Grant W, Martin Nicholas G, Medland Sarah |
Genome-wide association study of the child behavior checklist dysregulation profile.
Journal of the American Academy of Child and Adolescent Psychiatry 2011 Aug 50 (8): 807-17.e8. Mick Eric, McGough James, Loo Sandra, Doyle Alysa E, Wozniak Janet, Wilens Timothy E, Smalley Susan, McCracken James, Biederman Joseph, Faraone Stephen |
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation. PLoS genetics 2013 Apr 9 (4): e1003364. Nakano Yukiko, Chayama Kazuaki, Ochi Hidenori, Toshishige Masaaki, Hayashida Yasufumi, Miki Daiki, Hayes C Nelson, Suzuki Hidekazu, Tokuyama Takehito, Oda Noboru, Suenari Kazuyoshi, Uchimura-Makita Yuko, Kajihara Kenta, Sairaku Akinori, Motoda Chikaaki, Fujiwara Mai, Watanabe Yoshikazu, Yoshida Yukihiko, Ohkubo Kimie, Watanabe Ichiro, Nogami Akihiko, Hasegawa Kanae, Watanabe Hiroshi, Endo Naoto, Aiba Takeshi, Shimizu Wataru, Ohno Seiko, Horie Minoru, Arihiro Koji, Tashiro Satoshi, Makita Naomasa, Kihara Yasu |
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Annals of neurology 2014 Sep 76 (3): 379-92. Jun Gyungah, Asai Hirohide, Zeldich Ella, Drapeau Elodie, Chen CiDi, Chung Jaeyoon, Park Jong-Ho, Kim Sehwa, Haroutunian Vahram, Foroud Tatiana, Kuwano Ryozo, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard D, Lunetta Kathryn L, Kim Jong-Won, Buxbaum Joseph D, Mayeux Richard, Ikezu Tsuneya, Abraham Carmela R, Farrer Lindsay |
Effects of SEMA3 polymorphisms in Hirschsprung disease patients. Pediatric surgery international 2016 Nov 32 (11): 1025-1028. Gunadi , Makhmudi Akhmad, Agustriani Nunik, Rochad |
Next-generation sequencing of patients with congenital anosmia. European journal of human genetics : EJHG 2017 12 25 (12): 1377-1387. Alkelai Anna, Olender Tsviya, Dode Catherine, Shushan Sagit, Tatarskyy Pavel, Furman-Haran Edna, Boyko Valery, Gross-Isseroff Ruth, Halvorsen Matthew, Greenbaum Lior, Milgrom Roni, Yamada Kazuya, Haneishi Ayumi, Blau Ilan, Lancet Dor |
Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.
JAMA psychiatry 2017 Dec 74 (12): 1234-1241. Zhou Hang, Polimanti Renato, Yang Bao-Zhu, Wang Qian, Han Shizhong, Sherva Richard, Nuñez Yaira Z, Zhao Hongyu, Farrer Lindsay A, Kranzler Henry R, Gelernter Jo |
Semaphorin-3A, semaphorin-7A gene single nucleotide polymorphisms, and systemic lupus erythematosus susceptibility. Autoimmunity 2019 8 52 (4): 161-167. Liu Li-Na, Wang Peng, Zou Yan-Feng, Xu Zhiwei, Cheng Jian, Zhang Yuzhou, Hu Wenbiao, Pan Hai-Fe |
SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD). Frontiers in endocrinology 2020 7 11 368. Budny Bartlomiej, Zemojtel Tomasz, Kaluzna Malgorzata, Gut Pawel, Niedziela Marek, Obara-Moszynska Monika, Rabska-Pietrzak Barbara, Karmelita-Katulska Katarzyna, Stajgis Marek, Ambroziak Urszula, Bednarczuk Tomasz, Wrotkowska Elzbieta, Bukowska-Olech Ewelina, Jamsheer Aleksander, Ruchala Marek, Ziemnicka Katarzy |
Assessment of the genetic contribution to brain magnetic resonance imaging lesion load and atrophy measures in multiple sclerosis patients. European journal of neurology 2021 Apr . Clarelli Ferdinando, Assunta Rocca Maria, Santoro Silvia, De Meo Ermelinda, Ferrè Laura, Sorosina Melissa, Martinelli Boneschi Filippo, Esposito Federica, Filippi Massi |
Genome-wide epistasis analysis for Alzheimer's disease and implications for genetic risk prediction. Alzheimer's research & therapy 2021 03 13 (1): 55. Wang Hui, Bennett David A, De Jager Philip L, Zhang Qing-Ye, Zhang Hong- |
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review. Clinical endocrinology 2022 9 97 (6): 804-813. Patil Virendra A, Lila Anurag Ranjan, Shah Nalini, Arya Sneha, Sarathi Vijaya, Shah Ravikumar, Jadhav Swati S, Memon Saba Samad, Karlekar Manjiri, Bandgar Tush |
Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability. Frontiers in endocrinology 2022 3 13 810375. Li Jing, Zhong Yuxia, Guo Tao, Yu Yerong, Li Jianw |
Association between SEMA3A signaling pathway genes and BMD/OP risk: An epidemiological and experimental study. Frontiers in endocrinology 2022 11 13 1014431. Zhou Hao-Long, Wei Mu-Hong, Di Dong-Sheng, Zhang Ru-Yi, Zhang Jian-Li, Yuan Ting-Ting, Liu Qian, Zhou Ting-Ting, Huang Qin, Wang |
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