Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: JARID2[original query] |
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Positive association of schizophrenia to JARID2 gene. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jan 144B (1): 45-51. Pedrosa Erika, Ye Kenny, Nolan Karen A, Morrell Lauren, Okun Jeffrey M, Persky Adam D, Saito Takuya, Lachman Herbert |
Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Journal of biomedicine & biotechnology 2009 2009 536918. Liu Yang, Chen Gang, Norton Nadine, Liu Wenmin, Zhu Haining, Zhou Peng, Luan Meng, Yang Shulin, Chen Xing, Carroll Liam, Williams Nigel M, O'Donovan Michael C, Kirov George, Owen Michael |
Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder. Molecular autism 2012 3 (1): 4. Ramos Paula S, Sajuthi Satria, Langefeld Carl D, Walker Stephen |
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Autism research : official journal of the International Society for Autism Research 2015 Aug . Liu Xiaoxi, Shimada Takafumi, Otowa Takeshi, Wu Yu-Yu, Kawamura Yoshiya, Tochigi Mamoru, Iwata Yasuhide, Umekage Tadashi, Toyota Tomoko, Maekawa Motoko, Iwayama Yoshimi, Suzuki Katsuaki, Kakiuchi Chihiro, Kuwabara Hitoshi, Kano Yukiko, Nishida Hisami, Sugiyama Toshiro, Kato Nobumasa, Chen Chia-Hsiang, Mori Norio, Yamada Kazuo, Yoshikawa Takeo, Kasai Kiyoto, Tokunaga Katsushi, Sasaki Tsukasa, Gau Susan Shur-F |
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.
Nature communications 2016 07 7 12050. Mitchell Jonathan S, Li Ni, Weinhold Niels, Försti Asta, Ali Mina, van Duin Mark, Thorleifsson Gudmar, Johnson David C, Chen Bowang, Halvarsson Britt-Marie, Gudbjartsson Daniel F, Kuiper Rowan, Stephens Owen W, Bertsch Uta, Broderick Peter, Campo Chiara, Einsele Hermann, Gregory Walter A, Gullberg Urban, Henrion Marc, Hillengass Jens, Hoffmann Per, Jackson Graham H, Johnsson Ellinor, Jöud Magnus, Kristinsson Sigurður Y, Lenhoff Stig, Lenive Oleg, Mellqvist Ulf-Henrik, Migliorini Gabriele, Nahi Hareth, Nelander Sven, Nickel Jolanta, Nöthen Markus M, Rafnar Thorunn, Ross Fiona M, da Silva Filho Miguel Inacio, Swaminathan Bhairavi, Thomsen Hauke, Turesson Ingemar, Vangsted Annette, Vogel Ulla, Waage Anders, Walker Brian A, Wihlborg Anna-Karin, Broyl Annemiek, Davies Faith E, Thorsteinsdottir Unnur, Langer Christian, Hansson Markus, Kaiser Martin, Sonneveld Pieter, Stefansson Kari, Morgan Gareth J, Goldschmidt Hartmut, Hemminki Kari, Nilsson Björn, Houlston Richard |
Brazilian multicenter study of association between polymorphisms in CRISPLD2 and JARID2 and non-syndromic oral clefts. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2016 Jun . Messetti Ana Camila, Machado Renato Assis, de Oliveira Carine Ervolino, Martelli-Júnior Hercílio, de Almeida Reis Silvia Regina, Moreira Helenara Salvati Bertolossi, Persuhn Darlene Camati, Wu Tao, Coletta Ricardo |
Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease. Genes and immunity 2016 May . Long D, Deng X, Singh P, Loeb M, Lauring A S, Seielstad |
A Novel Relationship for Schizophrenia, Bipolar and Major Depressive Disorder Part 6: A Hint from Chromosome 6 High Density Association Screen. Current molecular medicine 2016 Nov . Chen X, Long F, Cai B, Chen X, Chen |
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease. PLoS genetics 2016 Oct 12 (10): e1006335. Preuss Christoph, Capredon Melanie, Wünnemann Florian, Chetaille Philippe, Prince Andrea, Godard Beatrice, Leclerc Severine, Sobreira Nara, Ling Hua, Awadalla Philip, Thibeault Maryse, Khairy Paul, , Samuels Mark E, Andelfinger Greg |
Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes. American journal of medical genetics. Part A 2016 Nov 170 (11): 2916-2926. Zahir Farah R, Tucker Tracy, Mayo Sonia, Brown Carolyn J, Lim Emilia L, Taylor Jonathan, Marra Marco A, Hamdan Fadi F, Michaud Jacques L, Friedman Jan |
A study of single nucleotide polymorphisms in CD157, AIM2 and JARID2 genes in Han Chinese children with autism spectrum disorder. Nordic journal of psychiatry 2017 Dec 1-5. Mo Weiming, Liu Jun, Zhang Zengyu, Yu Hong, Yang Aiping, Qu Fei, Hu Pingfang, Liu Zhuo, Hu Fengp |
Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
Possible effect of SNAIL family transcriptional repressor 1 polymorphisms in non-syndromic cleft lip with or without cleft palate. Clinical oral investigations 2018 Jan . Cura Francesca, Palmieri Annalisa, Girardi Ambra, Carinci Francesco, Morselli Paolo Giovanni, Nouri Nayereh, Pezzetti Furio, Scapoli Luca, Martinelli Marcel |
Novel LRRK2 mutations and other rare, non-BAP1-related candidate tumor predisposition gene variants in high-risk cancer families with mesothelioma and other tumors. Human molecular genetics 2021 5 30 (18): 1750-1761. Cheung Mitchell, Kadariya Yuwaraj, Sementino Eleonora, Hall Michael J, Cozzi Ilaria, Ascoli Valeria, Ohar Jill A, Testa Joseph |
Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510. Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl |
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- Page last updated:Apr 22, 2024
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