Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: CHRFAM7A[original query] |
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Association study of CHRFAM7A copy number and 2 bp deletion polymorphisms with schizophrenia and bipolar affective disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006 Sep 141B (6): 571-5. Flomen Rachel H, Collier David A, Osborne Sarah, Munro Janet, Breen Gerome, St Clair David, Makoff Andrew |
Linkage disequilibrium analysis of the CHRNA7 gene and its partially duplicated region in schizophrenia. Neuroscience research 2007 Feb 57 (2): 194-202. Iwata Yasuhide, Nakajima Mizuho, Yamada Kazuo, Nakamura Kazuhiko, Sekine Yoshimoto, Tsuchiya Kenji J, Sugihara Genichi, Matsuzaki Hideo, Suda Shiro, Suzuki Katsuaki, Takei Nori, Mori Norio, Iwayama Yoshimi, Takao Hitomi, Yoshikawa Takeo, Riley Brien, Makoff Andrew, Sham Pak, Chen Ronald, Collier Dav |
Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene. The American journal of psychiatry 2006 Oct 163 (10): 1832-4. Dempster Emma L, Toulopoulou Timothea, McDonald Colm, Bramon Elvira, Walshe Muriel, Wickham Harvey, Sham Pak C, Murray Robin M, Collier David |
Association between a genetic variant of the alpha-7 nicotinic acetylcholine receptor subunit and four types of dementia. Dementia and geriatric cognitive disorders 2009 28 (1): 56-62. Fehér Agnes, Juhász Anna, Rimanóczy Agnes, Csibri Eva, Kálmán János, Janka Zolt |
A 2-base pair deletion polymorphism in the partial duplication of the alpha7 nicotinic acetylcholine gene (CHRFAM7A) on chromosome 15q14 is associated with schizophrenia. Brain research 2009 Sep 1291 1-11. Sinkus Melissa L, Lee Michael J, Gault Judith, Logel Judith, Short Margaret, Freedman Robert, Christian Susan L, Lyon Jennifer, Leonard Sher |
Smoking in adult attention-deficit/hyperactivity disorder: interaction between 15q13 nicotinic genes and Temperament Character Inventory scores. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2010 Mar 11 (2 Pt 2): 506-10. Manchia Mirko, Viggiano Emanuela, Tiwari Arun K, Renou Julien, Jain Umesh, De Luca Vincenzo, Kennedy James |
CHRFAM7A copy number and 2-bp deletion polymorphisms and antisaccade performance. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2009 Mar 12 (2): 267-73. Petrovsky Nadine, Schmechtig Anne, Flomen Rachel H, Kumari Veena, Collier David, Makoff Andrew, Wagner Michael, Ettinger Ulri |
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. International journal of Alzheimer's disease 2011 2011 729478. Swaminathan Shanker, Kim Sungeun, Shen Li, Risacher Shannon L, Foroud Tatiana, Pankratz Nathan, Potkin Steven G, Huentelman Matthew J, Craig David W, Weiner Michael W, Saykin Andrew J, The Alzheimer's Disease Neuroimaging Initiative Adn |
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 |
Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating. European journal of human genetics : EJHG 2013 Jan 21 (1): 76-81. Flomen Rachel H, Shaikh Madiha, Walshe Muriel, Schulze Katja, Hall Mei-Hua, Picchioni Marco, Rijsdijk Fruhling, Toulopoulou Timothea, Kravariti Eugenia, Murray Robin M, Asherson Philip, Makoff Andrew J, Bramon Elvi |
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, , |
Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. PloS one 2012 7 (12): e50640. Swaminathan Shanker, Huentelman Matthew J, Corneveaux Jason J, Myers Amanda J, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Shen Li, Kim Sungeun, Turk Mari, Hardy John, Reiman Eric M, Saykin Andrew J, |
Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy. DNA and cell biology 2013 Nov 32 (11): 640-7. Rozycka Agata, Dorszewska Jolanta, Steinborn Barbara, Lianeri Margarita, Winczewska-Wiktor Anna, Sniezawska Aleksandra, Wisniewska Kamila, Jagodzinski Pawel |
CHRNA7 and CHRFAM7A mRNAs: co-localized and their expression levels altered in the postmortem dorsolateral prefrontal cortex in major psychiatric disorders. The American journal of psychiatry 2015 Jul appiajp201514080978. Kunii Yasuto, Zhang Wenyu, Xu Qing, Hyde Thomas M, McFadden Whitney, Shin Joo Heon, Deep-Soboslay Amy, Ye Tianzhang, Li Chao, Kleinman Joel E, Wang Kuan Hong, Lipska Barbara |
Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility. American journal of medical genetics. Part A 2015 Apr 167A (4): 715-23. Bacchelli Elena, Battaglia Agatino, Cameli Cinzia, Lomartire Silvia, Tancredi Raffaella, Thomson Susanne, Sutcliffe James S, Maestrini Ele |
Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy. Epilepsy research 2015 Sep 117 70-73. Damiano John A, Mullen Saul A, Hildebrand Michael S, Bellows Susannah T, Lawrence Kate M, Arsov Todor, Dibbens Leanne, Major Heather, Dahl Hans-Henrik M, Mefford Heather C, Darbro Benjamin W, Scheffer Ingrid E, Berkovic Samuel |
Copy Number Variations in Adult-onset Neuropsychiatric Diseases. Current genomics 2018 9 19 (6): 420-430. Lew Alexandra R, Kellermayer Timot R, Sule Balint P, Szigeti Kin |
Genetic variation in CHRNA7 and CHRFAM7A is associated with nicotine dependence and response to varenicline treatment. European journal of human genetics : EJHG 2018 Aug . Cameli Cinzia, Bacchelli Elena, De Paola Maria, Giucastro Giuliano, Cifiello Stefano, Collo Ginetta, Cainazzo Maria Michela, Pini Luigi Alberto, Maestrini Elena, Zoli Miche |
Association of a Functional Polymorphism in the CHRFAM7A Gene with Inflammatory Response Mediators and Neuropathic Pain after Spinal Cord Injury. Journal of neurotrauma 2019 Mar . Huang Wan, Kabbani Nadine, Brannan Tricia K, Lin Ming Kuan, Theiss Mark M, Hamilton John F, Ecklund James M, Conley Yvette P, Vodovotz Yoram, Brienza David, Wagner Amy K, Robbins Emily, Sowa Gwendolyn A, Lipsky Robert |
Effect of CHRFAM7A ?2bp gene variant on secondary inflammation after spinal cord injury. PloS one 2021 5 16 (5): e0251110. Lin Mingkuan, Huang Wan, Kabbani Nadine, Theiss Mark M, Hamilton John F, Ecklund James M, Conley Yvette P, Vodovotz Yoram, Brienza David, Wagner Amy K, Robbins Emily, Sowa Gwendolyn A, Lipsky Robert |
Polymorphisms in alpha 7 nicotinic acetylcholine receptor gene, CHRNA7, and its partially duplicated gene, CHRFAM7A, associate with increased inflammatory response in human peripheral mononuclear cells. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2022 3 36 (5): e22271. Pattanaik Bagmi, Hammarlund Maria, Mjörnstedt Filip, Ulleryd Marcus A, Zhong Wen, Uhlén Mathias, Gummesson Anders, Bergström Göran, Johansson Maria |
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- Page last updated:Apr 16, 2024
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