Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: HDAC4[original query] |
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High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts. Journal of medical genetics 2006 Jul 43 (7): 598-608. Park J W, Cai J, McIntosh I, Jabs E W, Fallin M D, Ingersoll R, Hetmanski J B, Vekemans M, Attie-Bitach T, Lovett M, Scott A F, Beaty T |
Multi-ethnic genetic association study of carotid intima-media thickness using a targeted cardiovascular SNP microarray. Stroke; a journal of cerebral circulation 2009 Oct 40 (10): 3173-9. Lanktree Matthew B, Hegele Robert A, Yusuf Salim, Anand Sonia |
Association of histone deacetylase genes with schizophrenia in Korean population. Psychiatry research 2010 Jul 178 (2): 266-9. Kim Tae, Park Jin Kyung, Kim Hak-Jae, Chung Joo-Ho, Kim Jong W |
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
Common genetic variants related to genomic integrity and risk of papillary thyroid cancer. Carcinogenesis 2011 Aug 32 (8): 1231-7. Neta Gila, Brenner Alina V, Sturgis Erich M, Pfeiffer Ruth M, Hutchinson Amy A, Aschebrook-Kilfoy Briseis, Yeager Meredith, Xu Li, Wheeler William, Abend Michael, Ron Elaine, Tucker Margaret A, Chanock Stephen J, Sigurdson Alice |
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity. Journal of human genetics 2012 Apr 57 (4): 277-9. Izzi Benedetta, de Zegher Francis, Francois Inge, del Favero Jurgen, Goossens Dirk, Wittevrongel Christine, Thys Chantal, Van Geet Chris, Freson Kathle |
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American journal of human genetics 2014 May 94 (5): 677-94. Pinto Dalila, Delaby Elsa, Merico Daniele, Barbosa Mafalda, Merikangas Alison, Klei Lambertus, Thiruvahindrapuram Bhooma, Xu Xiao, Ziman Robert, Wang Zhuozhi, Vorstman Jacob A S, Thompson Ann, Regan Regina, Pilorge Marion, Pellecchia Giovanna, Pagnamenta Alistair T, Oliveira Bárbara, Marshall Christian R, Magalhaes Tiago R, Lowe Jennifer K, Howe Jennifer L, Griswold Anthony J, Gilbert John, Duketis Eftichia, Dombroski Beth A, De Jonge Maretha V, Cuccaro Michael, Crawford Emily L, Correia Catarina T, Conroy Judith, Conceição Inês C, Chiocchetti Andreas G, Casey Jillian P, Cai Guiqing, Cabrol Christelle, Bolshakova Nadia, Bacchelli Elena, Anney Richard, Gallinger Steven, Cotterchio Michelle, Casey Graham, Zwaigenbaum Lonnie, Wittemeyer Kerstin, Wing Kirsty, Wallace Simon, van Engeland Herman, Tryfon Ana, Thomson Susanne, Soorya Latha, Rogé Bernadette, Roberts Wendy, Poustka Fritz, Mouga Susana, Minshew Nancy, McInnes L Alison, McGrew Susan G, Lord Catherine, Leboyer Marion, Le Couteur Ann S, Kolevzon Alexander, Jiménez González Patricia, Jacob Suma, Holt Richard, Guter Stephen, Green Jonathan, Green Andrew, Gillberg Christopher, Fernandez Bridget A, Duque Frederico, Delorme Richard, Dawson Geraldine, Chaste Pauline, Café Cátia, Brennan Sean, Bourgeron Thomas, Bolton Patrick F, Bölte Sven, Bernier Raphael, Baird Gillian, Bailey Anthony J, Anagnostou Evdokia, Almeida Joana, Wijsman Ellen M, Vieland Veronica J, Vicente Astrid M, Schellenberg Gerard D, Pericak-Vance Margaret, Paterson Andrew D, Parr Jeremy R, Oliveira Guiomar, Nurnberger John I, Monaco Anthony P, Maestrini Elena, Klauck Sabine M, Hakonarson Hakon, Haines Jonathan L, Geschwind Daniel H, Freitag Christine M, Folstein Susan E, Ennis Sean, Coon Hilary, Battaglia Agatino, Szatmari Peter, Sutcliffe James S, Hallmayer Joachim, Gill Michael, Cook Edwin H, Buxbaum Joseph D, Devlin Bernie, Gallagher Louise, Betancur Catalina, Scherer Stephen |
Fine-mapping the 2q37 and 17q11.2-q22 loci for novel genes and sequence variants associated with a genetic predisposition to prostate cancer. International journal of cancer. Journal international du cancer 2015 May 136 (10): 2316-27. Laitinen Virpi H, Rantapero Tommi, Fischer Daniel, Vuorinen Elisa M, Tammela Teuvo L J, , Wahlfors Tiina, Schleutker Johan |
A Comprehensive Meta-analysis of Case-Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 Feb . Figlioli Gisella, Elisei Rossella, Romei Cristina, Melaiu Ombretta, Cipollini Monica, Bambi Franco, Chen Bowang, Köhler Aleksandra, Cristaudo Alfonso, Hemminki Kari, Gemignani Federica, Försti Asta, Landi Stefa |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Molecular autism 2017 8 21. Authors are not available |
Kruppel-like factor4 regulates PRDM1 expression through binding to an autoimmune risk allele. JCI insight 2017 1 2 (1): e89569. Jang Su Hwa, Chen Helen, Gregersen Peter K, Diamond Betty, Kim Sun Ju |
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
Nature communications 2018 11 9 (1): 4774. Duffy David L, Zhu Gu, Li Xin, Sanna Marianna, Iles Mark M, Jacobs Leonie C, Evans David M, Yazar Seyhan, Beesley Jonathan, Law Matthew H, Kraft Peter, Visconti Alessia, Taylor John C, Liu Fan, Wright Margaret J, Henders Anjali K, Bowdler Lisa, Glass Dan, Ikram M Arfan, Uitterlinden André G, Madden Pamela A, Heath Andrew C, Nelson Elliot C, Green Adele C, Chanock Stephen, Barrett Jennifer H, Brown Matthew A, Hayward Nicholas K, MacGregor Stuart, Sturm Richard A, Hewitt Alex W, , Kayser Manfred, Hunter David J, Newton Bishop Julia A, Spector Timothy D, Montgomery Grant W, Mackey David A, Smith George Davey, Nijsten Tamar E, Bishop D Timothy, Bataille Veronique, Falchi Mario, Han Jiali, Martin Nicholas |
Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time.
Translational psychiatry 2018 10 8 (1): 207. Pinar Ari, Hawi Ziarih, Cummins Tarrant, Johnson Beth, Pauper Marc, Tong Janette, Tiego Jeggan, Finlay Amy, Klein Marieke, Franke Barbara, Fornito Alex, Bellgrove Mark |
Identification of Prolificacy-Related Differentially Expressed Proteins from Sheep (Ovis aries) Hypothalamus by Comparative Proteomics. Proteomics 2019 5 19 (14): e1900118. Zhang Zhuangbiao, Tang Jishun, Di Ran, Liu Qiuyue, Wang Xiangyu, Gan Shangquan, Zhang Xiaosheng, Zhang Jinlong, Chen Wei, Hu Wenping, Chu Mingxi |
Epigenetic Modifications in Placenta are Associated with the Child's Sensitization to Allergens. BioMed research international 2019 5 2019 1315257. Harb Hani, Alashkar Alhamwe Bilal, Acevedo Nathalie, Frumento Paolo, Johansson Catharina, Eick Lisa, Papadogiannakis Nikos, Alm Johan, Renz Harald, Potaczek Daniel P, Scheynius Anni |
Hot Spot TERT Promoter Mutations Are Rare in Sporadic Pancreatic Neuroendocrine Neoplasms and Associated with Telomere Length and Epigenetic Expression Patterns. Cancers 2020 6 12 (6): . Posch Alexandra, Hofer-Zeni Sarah, Klieser Eckhard, Primavesi Florian, Naderlinger Elisabeth, Brandstetter Anita, Filipits Martin, Urbas Romana, Swiercynski Stefan, Jäger Tarkan, Winkelmann Paul, Kiesslich Tobias, Lu Lingeng, Neureiter Daniel, Stättner Stefan, Holzmann Kla |
The Liability Threshold Model for Predicting the Risk of Cardiovascular Disease in Patients with Type 2 Diabetes: A Multi-Cohort Study of Korean Adults. Metabolites 2020 Dec 11 (1): . Hong Eun Pyo, Heo Seong Gu, Park Ji W |
Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients. Scientific reports 2020 12 10 (1): 22217. Maltby Vicki E, Lea Rodney A, Burnard Sean, Xavier Alexandre, Van Cao Thao, White Nicole, Kennedy Daniel, Groen Kira, Sanders Katherine A, Seeto Rebecca, Bray Samara, Gresle Melissa, Laverick Louise, Butzkueven Helmut, Scott Rodney J, Lechner-Scott Jeannet |
Link between obsessive-compulsive disorder and polymorphisms in HDAC genes. Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999) 2021 Oct . Dondu Ayse, Caliskan Metin, Orenay-Boyacioglu Se |
Exome Sequencing Reveals De Novo Variants in Congenital Scoliosis. Journal of pediatric genetics 2022 10 11 (4): 287-291. Murakami Kohei, Kikugawa Shingo, Seki Shoji, Terai Hidetomi, Suzuki Takako, Nakano Masaki, Takahashi Jun, Nakamura Yuk |
Myeloid/Lymphoid Neoplasm with FGFR1 Rearrangement Presenting with Polycythemia Vera and T-cell Acute Lymphoblastic Leukemia. Cancer genetics 2023 7 276-277 43-47. Lisa M Marinelli, Joshua T Romain, William Ehman, Veronica Ortega, Gopalrao Velagaleti, Thomas F Gibbons, Ashley Nazario-Toole, Allen R Holm |
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- Page last updated:Apr 22, 2024
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