Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: EMD[original query] |
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MYOC mutation frequency in primary open-angle glaucoma patients from Western Switzerland. Ophthalmic genetics 2002 1 22 (4): 225-31. Mataftsi A, Achache F, Héon E, Mermoud A, Cousin P, Metthez G, Schorderet D F, Munier F |
Polymorphism in the growth hormone gene, weight in infancy, and adult bone mass. The Journal of clinical endocrinology and metabolism 2004 Oct 89 (10): 4898-903. Dennison E M, Syddall H E, Rodriguez S, Voropanov A, Day I N M, Cooper C, |
Polymorphisms of the IL-1 gene complex are associated with alcohol dependence in Spanish Caucasians: data from an association study. Alcoholism, clinical and experimental research 2009 Dec 33 (12): 2147-53. Saiz Pilar A, Garcia-Portilla Maria P, Florez Gerardo, Corcoran Paul, Arango Celso, Morales Blanca, Leza Juan C, Alvarez Sandra, Díaz Eva M, Alvarez Victoria, Coto Eliecer, Nogueiras Luis, Bobes Jul |
Emotional disorders in testicular cancer survivors in relation to hypogonadism, androgen receptor polymorphism and treatment modality. Journal of affective disorders 2010 May 122 (3): 260-6. Eberhard Jakob, Ståhl Olof, Cohn-Cedermark Gabriella, Cavallin-Ståhl Eva, Giwercman Yvonne, Rastkhani Hamideh, Rylander Lars, Eberhard-Gran Malin, Kvist Ulrik, Giwercman Aleksand |
Novel and recurrent EMD mutations in patients with Emery-Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot. Journal of human genetics 2011 Jun . Brown CA, Scharner J, Felice K, Meriggioli MN, Tarnopolsky M, Bower M, Zammit PS, Mendell JR, Ellis JA |
Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological psychiatry 2012 Oct . Terwisscha van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer-Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA, Kahn RS |
SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength. Diabetes 2014 Jan 63 (1): 363-8. Sprouse Courtney, Gordish-Dressman Heather, Orkunoglu-Suer E Funda, Lipof Jason S, Moeckel-Cole Stephanie, Patel Ronak R, Adham Kasra, Larkin Justin S, Hubal Monica J, Kearns Amy K, Clarkson Priscilla M, Thompson Paul D, Angelopoulos Theodore J, Gordon Paul M, Moyna Niall M, Pescatello Linda S, Visich Paul S, Zoeller Robert F, Hoffman Eric P, Tosi Laura L, Devaney Joseph |
Association of dopamine gene variants, emotion dysregulation and ADHD in autism spectrum disorder. Research in developmental disabilities 2014 Jul 35 (7): 1658-65. Gadow Kenneth D, Pinsonneault Julia K, Perlman Greg, Sadee Wolfga |
Genetic and environmental risk factors for extramacular drusen. Molecular vision 2020 26 661-669. Altay Lebriz, Subiras Xavier, Lorés de Motta Laura, Schick Tina, Berghold Aileen, Hoyng Carel B, den Hollander Anneke I, Fauser Sascha, Sadda Srinivas R, Liakopoulos Sand |
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases. Cardiovascular research 2020 1 116 (13): 2116-2130. Hayashi Kenshi, Teramoto Ryota, Nomura Akihiro, Asano Yoshihiro, Beerens Manu, Kurata Yasutaka, Kobayashi Isao, Fujino Noboru, Furusho Hiroshi, Sakata Kenji, Onoue Kenji, Chiang David Y, Kiviniemi Tuomas O, Buys Eva, Sips Patrick, Burch Micah L, Zhao Yanbin, Kelly Amy E, Namura Masanobu, Kita Yoshihito, Tsuchiya Taketsugu, Kaku Bunji, Oe Kotaro, Takeda Yuko, Konno Tetsuo, Inoue Masaru, Fujita Takashi, Kato Takeshi, Funada Akira, Tada Hayato, Hodatsu Akihiko, Nakanishi Chiaki, Sakamoto Yuichiro, Tsuda Toyonobu, Nagata Yoji, Tanaka Yoshihiro, Okada Hirofumi, Usuda Keisuke, Cui Shihe, Saito Yoshihiko, MacRae Calum A, Takashima Seiji, Yamagishi Masakazu, Kawashiri Masa-Aki, Takamura Masayu |
The effect of polymorphisms in FSHR and FSHB genes on ovarian response: a prospective multicenter multinational study in Europe and Asia. Human reproduction (Oxford, England) 2021 Apr . Polyzos Nikolaos P, Neves A R, Drakopoulos P, Spits C, Alvaro Mercadal B, Garcia S, Ma P Q M, Le L H, Ho M T, Mertens J, Stoop D, Tournaye H, Vuong N |
Echocardiographic Features of Cardiomyopathy in Emery-Dreifuss Muscular Dystrophy. Cardiology research and practice 2021 2 2021 8812044. Marchel Micha?, Madej-Pilarczyk Agnieszka, Tymi?ska Agata, Steckiewicz Roman, Kochanowski Janusz, Wysi?ska Julia, Ostrowska Ewa, Balsam Pawe?, Grabowski Marcin, Opolski Grzego |
The effect of polymorphisms in FSHR gene on late follicular phase progesterone and estradiol serum levels in predicted normoresponders. Human reproduction (Oxford, England) 2022 Sep . Neves A R, Vuong N L, Blockeel C, Garcia S, Alviggi C, Spits C, Ma P Q M, Ho M T, Tournaye H, Polyzos N |
Favorable Activity and Safety Profile of Memory-Enriched CD19-Targeted Chimeric Antigen Receptor T-Cell Therapy in Adults with High-Risk Relapsed/Refractory ALL. Clinical cancer research : an official journal of the American Association for Cancer Research 2022 10 29 (4): 742-753. Aldoss Ibrahim, Khaled Samer K, Wang Xiuli, Palmer Joycelynne, Wang Yan, Wagner Jamie R, Clark Mary C, Simpson Jennifer, Paul Jinny, Vyas Vibhuti, Chien Sheng-Hsuan, Stein Anthony, Pullarkat Vinod, Salhotra Amandeep, Al Malki Monzr M, Aribi Ahmed, Sandhu Karamjeet, Thomas Sandra H, Budde Lihua E, Marcucci Guido, Brown Christine E, Forman Stephen |
Levels of Angiotensin-Converting Enzyme and Apolipoproteins Are Associated with Alzheimer's Disease and Cardiovascular Diseases. Cells 2022 1 11 (1): . Xu Chun, Garcia Debra, Lu Yongke, Ozuna Kaysie, Adjeroh Donald A, Wang Kesheng, On Behalf Of The Alzheimer's Disease Neuroimaging Initiativ |
Identification of mutations on the EMD and EYA4 genes associated with Emery-Dreifuss muscular dystrophy and deafness: a case report. Frontiers in neurology 2023 5 14 1183147. Ana Karina Zambrano, Elius Paz-Cruz, Santiago Cadena-Ullauri, Patricia Guevara-Ramírez, Viviana A Ruiz-Pozo, Rafael Tamayo-Trujillo, Rita Ibarra-Castillo, José Luis Laso-Bayas, Nieves Doménech, Adriana Alexandra Ibarra-Rodríguez, Ricardo Hidal |
Clinical and genomic characterization of Chinese patients with functional high-risk multiple myeloma: A real-world validation study. Frontiers in oncology 2023 3 13 1110693. Wang Yu-Tong, Chu Bin, Zhou Tian-Guan, Lu Min-Qiu, Shi Lei, Gao Shan, Fang Li-Juan, Xiang Qiu-Qing, Zhao Xin-, Wang Meng-Zhen, Sun Kai, Bao |
Cytogenetic and survival analysis in 315 multiple myeloma patients; five with orbital and eight with extramedullary disease. Orbit (Amsterdam, Netherlands) 2023 1 1-9. Tucker Susan M, Zaihra Tasne |
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- Page last updated:Apr 16, 2024
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