Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: SGCD[original query] |
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Genome-wide association study of anthropometric traits in Korcula Island, Croatia.
Croatian medical journal 2009 Feb 50 (1): 7-16. Polasek Ozren, Marusi? Ana, Rotim Kresimir, Hayward Caroline, Vitart Veronique, Huffman Jennifer, Campbell Susan, Jankovi? Stipan, Boban Mladen, Biloglav Zrinka, Kolci? Ivana, Krzelj Vjekoslav, Terzi? Janos, Matec Lana, Tometi? Gordan, Nonkovi? Dijana, Nincevi? Jasna, Pehli? Marina, Zedelj Jurica, Velagi? Vedran, Jurici? Danica, Kirac Iva, Belak Kovacevi? Sanja, Wright Alan F, Campbell Harry, Rudan Ig |
Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration. BMC research notes 2010 3 (1): 26. Lin Wan-Yu, Lee Wen-Chu |
Large-scale candidate gene analysis of HDL particle features. PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease.
American journal of respiratory cell and molecular biology 2015 Aug 53 (2): 226-34. Hansel Nadia N, Paré Peter D, Rafaels Nicholas, Sin Don D, Sandford Andrew, Daley Denise, Vergara Candelaria, Huang Lili, Elliott W Mark, Pascoe Chris D, Arsenault Bryna A, Postma Dirkje S, Boezen H Marike, Bossé Yohan, van den Berge Maarten, Hiemstra Pieter S, Cho Michael H, Litonjua Augusto A, Sparrow David, Ober Carole, Wise Robert A, Connett John, Neptune Enid R, Beaty Terri H, Ruczinski Ingo, Mathias Rasika A, Barnes Kathleen C, |
Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. Genes 2018 9 9 (10): . Perez-Ortiz Andric Christopher, Luna-Angulo Alexandra, Zenteno Juan Carlos, Rendon Alvaro, Cortes-Ballinas Liliana Guadalupe, Jimenez-Collado David, Antonio-Aguirre Bani, Peralta-Ildefonso Martha Janneth, Ramírez Israel, Jacob-Kuttothara Stefany, Estrada-Mena Francisco Javi |
Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. Clinical genetics 2019 3 96 (2): 126-133. Ten Dam Leroy, Frankhuizen Wendy S, Linssen Wim H J P, Straathof Chiara S, Niks Erik H, Faber Karin, Fock Annemarie, Kuks Jan B, Brusse Esther, de Coo René, Voermans Nicol, Verrips Aad, Hoogendijk Jessica E, van der Pol Ludo, Westra Dineke, de Visser Marianne, van der Kooi Anneke J, Ginjaar Ie |
Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients. Orphanet journal of rare diseases 2019 2 14 (1): 43. Xie Zhiying, Hou Yue, Yu Meng, Liu Yilin, Fan Yanbin, Zhang Wei, Wang Zhaoxia, Xiong Hui, Yuan Y |
Glucagon-like peptide-1 receptor and sarcoglycan delta genetic variants can affect cardiovascular risk in chronic kidney disease patients under hemodialysis. Clinical kidney journal 2020 9 13 (4): 666-673. Terranegra Annalisa, Arcidiacono Teresa, Macrina Lorenza, Brasacchio Caterina, Pivari Francesca, Mingione Alessandra, Tomei Sara, Mezzavilla Massimo, Silcock Lee, Cozzolino Mario, Palmieri Nicola, Conte Ferruccio, Sirtori Marcella, Rubinacci Alessandro, Soldati Laura, Vezzoli Giusep |
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy. Brain : a journal of neurology 2020 9 143 (9): 2696-2708. Alonso-Pérez Jorge, González-Quereda Lidia, Bello Luca, Guglieri Michela, Straub Volker, Gallano Pia, Semplicini Claudio, Pegoraro Elena, Zangaro Vittoria, Nascimento Andrés, Ortez Carlos, Comi Giacomo Pietro, Dam Leroy Ten, De Visser Marianne, van der Kooi A J, Garrido Cristina, Santos Manuela, Schara Ulrike, Gangfuß Andrea, Løkken Nicoline, Storgaard Jesper Helbo, Vissing John, Schoser Benedikt, Dekomien Gabriele, Udd Bjarne, Palmio Johanna, D'Amico Adele, Politano Luisa, Nigro Vincenzo, Bruno Claudio, Panicucci Chiara, Sarkozy Anna, Abdel-Mannan Omar, Alonso-Jimenez Alicia, Claeys Kristl G, Gomez-Andrés David, Munell Francina, Costa-Comellas Laura, Haberlová Jana, Rohlenová Marie, Elke De Vos, De Bleecker Jan L, Dominguez-González Cristina, Tasca Giorgio, Weiss Claudia, Deconinck Nicolas, Fernández-Torrón Roberto, López de Munain Adolfo, Camacho-Salas Ana, Melegh Béla, Hadzsiev Kinga, Leonardis Lea, Koritnik Blaz, Garibaldi Matteo, de Leon-Hernández Juan Carlos, Malfatti Edoardo, Fraga-Bau Arturo, Richard Isabelle, Illa Isabel, Díaz-Manera Jor |
Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Cancers 2021 Feb 13 (4): . Adjei Araba A, Lopez Camden L, Schaid Daniel J, Sloan Jeff A, Le-Rademacher Jennifer G, Loprinzi Charles L, Norman Aaron D, Olson Janet E, Couch Fergus J, Beutler Andreas S, Vachon Celine M, Ruddy Kathryn |
Identification of a SGCD × Discrimination Interaction Effect on Systolic Blood Pressure in African American Adults in the Jackson Heart Study. American journal of hypertension 2022 Aug . Hsiao Chu J, Dumeny Leanne, Bress Adam P, Johnson Dayna A, Shimbo Daichi, Cavallari Larisa H, Mulligan Connie |
Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A?>?C. Neurogenetics 2022 4 23 (3): 187-202. Bardhan Mainak, Anjanappa Ram Murthy, Polavarapu Kiran, Preethish-Kumar Veeramani, Vengalil Seena, Nashi Saraswati, Sanga Shamita, Padmanabh Hansashree, Valasani Ravi Kiran, Nishadham Vikas, Keerthipriya Muddasu, Geetha Thenral S, Ramprasad Vedam, Arunachal Gautham, Thomas Priya Treesa, Acharya Moulinath, Nalini Atchayar |
Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study. Annals of translational medicine 2022 3 10 (3): 129. Shen Cheng, Xu Lei, Sun Xiaoning, Sun Aijun, Ge Jun |
Genetic spectrum of sarcoglycanopathies in a cohort of Russian patients. Gene 2024 6 927 148680. Maria Bulakh, Daria Polyakova, Elena Dadali, Galina Rudenskaya, Inna Sharkova, Tatiana Markova, Aysylu Murtazina, Nina Demina, Sergei Kurbatov, Natalia Nikitina, Vasilisa Udalova, Aleksander Polyakov, Oxana Ryzhko |
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