Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: IMMP2L[original query] |
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Molecular psychiatry 2010 Jun 15 (6): 637-46. Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P |
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular psychiatry 2010 Sep 15 (9): 954-68. Maestrini E, Pagnamenta A T, Lamb J A, Bacchelli E, Sykes N H, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri T S, Minopoli F, Reichert J, Cai G, Buxbaum J D, Korvatska O, Schellenberg G D, Dawson G, de Bildt A, Minderaa R B, Mulder E J, Morris A P, Bailey A J, Monaco A P, |
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological psychiatry 2010 Aug 68 (4): 320-8. Pagnamenta Alistair T, Bacchelli Elena, de Jonge Maretha V, Mirza Ghazala, Scerri Thomas S, Minopoli Fiorella, Chiocchetti Andreas, Ludwig Kerstin U, Hoffmann Per, Paracchini Silvia, Lowy Ernesto, Harold Denise H, Chapman Jade A, Klauck Sabine M, Poustka Fritz, Houben Renske H, Staal Wouter G, Ophoff Roel A, O'Donovan Michael C, Williams Julie, Nöthen Markus M, Schulte-Körne Gerd, Deloukas Panos, Ragoussis Jiannis, Bailey Anthony J, Maestrini Elena, Monaco Anthony P, |
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human genetics 2012 Apr 131 (4): 565-79. Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid, Ennis Se |
Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Current Alzheimer research 2012 Sep 9 (7): 801-14. Swaminathan Shanker, Shen Li, Kim Sungeun, Inlow Mark, West John D, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Saykin Andrew J, , |
Genome-wide association study on differentiated thyroid cancer.
The Journal of clinical endocrinology and metabolism 2013 Oct 98 (10): E1674-81. Köhler Aleksandra, Chen Bowang, Gemignani Federica, Elisei Rossella, Romei Cristina, Figlioli Gisella, Cipollini Monica, Cristaudo Alfonso, Bambi Franco, Hoffmann Per, Herms Stefan, Kalemba Michal, Kula Dorota, Harris Shelley, Broderick Peter, Houlston Richard, Pastor Susana, Marcos Ricard, Velázquez Antonia, Jarzab Barbara, Hemminki Kari, Landi Stefano, Försti As |
Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population. Journal of Zhejiang University. Science. B 2014 Mar 15 (3): 264-71. Liang Shuang, Wang Xue-lai, Zou Ming-yang, Wang Han, Zhou Xue, Sun Cai-hong, Xia Wei, Wu Li-jie, Fujisawa Takashi X, Tomoda Ake |
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. European journal of human genetics : EJHG 2014 Nov 22 (11): 1283-9. Bertelsen Birgitte, Melchior Linea, Jensen Lars R, Groth Camilla, Glenthøj Birte, Rizzo Renata, Debes Nanette Mol, Skov Liselotte, Brøndum-Nielsen Karen, Paschou Peristera, Silahtaroglu Asli, Tümer Zeyn |
Genome-wide association study of schizophrenia in Ashkenazi Jews.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Jul . Goes Fernando S, McGrath John, Avramopoulos Dimitrios, Wolyniec Paula, Pirooznia Mehdi, Ruczinski Ingo, Nestadt Gerald, Kenny Eimear E, Vacic Vladimir, Peters Inga, Lencz Todd, Darvasi Ariel, Mulle Jennifer G, Warren Stephen T, Pulver Ann |
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 |
Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
Genome-wide association study of sepsis in extremely premature infants.
Archives of disease in childhood. Fetal and neonatal edition 2017 Mar . Srinivasan Lakshmi, Page Grier, Kirpalani Haresh, Murray Jeffrey C, Das Abhik, Higgins Rosemary D, Carlo Waldemar A, Bell Edward F, Goldberg Ronald N, Schibler Kurt, Sood Beena G, Stevenson David K, Stoll Barbara J, Van Meurs Krisa P, Johnson Karen J, Levy Joshua, McDonald Scott A, Zaterka-Baxter Kristin M, Kennedy Kathleen A, Sánchez Pablo J, Duara Shahnaz, Walsh Michele C, Shankaran Seetha, Wynn James L, Cotten C Michael, |
Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Nov . Zhang Yanqing, Liu Yi, Zarrei Mehdi, Tong Winnie, Dong Rui, Wang Ying, Zhang Haiyan, Yang Xiaomeng, MacDonald Jeffrey R, Uddin Mohammed, Scherer Stephen W, Gai Zhongt |
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. PloS one 2018 13 (6): e0199178. Lucas Sionne E M, Zhou Tiger, Blackburn Nicholas B, Mills Richard A, Ellis Jonathan, Leo Paul, Souzeau Emmanuelle, Ridge Bronwyn, Charlesworth Jac C, Lindsay Richard, Craig Jamie E, Burdon Kathryn |
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder. Cytogenetic and genome research 2018 5 154 (4): 196-200. Baldan Federica, Gnan Chiara, Franzoni Alessandra, Ferino Lucia, Allegri Lorenzo, Passon Nadia, Damante Giusep |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Frontiers in neurology 2020 9 11 803. Pagliaroli Luca, Vereczkei Andrea, Padmanabhuni Shanmukha Sampath, Tarnok Zsanett, Farkas Luca, Nagy Peter, Rizzo Renata, Wolanczyk Tomasz, Szymanska Urszula, Kapisyzi Mira, Basha Entela, Koumoula Anastasia, Androutsos Christos, Tsironi Vaia, Karagiannidis Iordanis, Paschou Peristera, Barta Csa |
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- Page last updated:Apr 29, 2024
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