Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: FRAS1[original query] |
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A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.
Obesity (Silver Spring, Md.) 2013 Jan . Li WD, Jiao H, Wang K, Zhang CK, Glessner JT, Grant SF, Zhao H, Hakonarson H, Arlen Price R |
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract. Journal of the American Society of Nephrology : JASN 2014 Sep 25 (9): 1917-22. Kohl Stefan, Hwang Daw-Yang, Dworschak Gabriel C, Hilger Alina C, Saisawat Pawaree, Vivante Asaf, Stajic Natasa, Bogdanovic Radovan, Reutter Heiko M, Kehinde Elijah O, Tasic Velibor, Hildebrandt Friedhe |
Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans. Forensic science international. Genetics 2015 Sep 19 280-288. Po?piech Ewelina, Kar?owska-Pik Joanna, Marci?ska Magdalena, Abidi Sarah, Andersen Jeppe Dyrberg, Berge Margreet van den, Carracedo Ángel, Eduardoff Mayra, Freire-Aradas Ana, Morling Niels, Sijen Titia, Skowron Ma?gorzata, Söchtig Jens, Syndercombe-Court Denise, Weiler Natalie, Schneider Peter M, Ballard David, Børsting Claus, Parson Walther, Phillips Chris, Branicki Wojciech, |
FRAS1-related extracellular matrix 3 (FREM3) single-nucleotide polymorphism effects on gene expression, amygdala reactivity and perceptual processing speed: An accelerated aging pathway of depression risk. Frontiers in psychology 2015 6 1377. Nikolova Yuliya S, Iruku Swetha P, Lin Chien-Wei, Conley Emily Drabant, Puralewski Rachel, French Beverly, Hariri Ahmad R, Sibille Etien |
Common polymorphisms in WNT10A affect tooth morphology as well as hair shape. Human molecular genetics 2015 May 24 (9): 2673-80. Kimura Ryosuke, Watanabe Chiaki, Kawaguchi Akira, Kim Yong-Il, Park Soo-Byung, Maki Koutaro, Ishida Hajime, Yamaguchi Tetsuta |
Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.
Frontiers in genetics 2016 7 37. Fridley Brooke L, Ghosh Taraswi M, Wang Alice, Raghavan Rama, Dai Junqiang, Goode Ellen L, Lamba Jatinder |
Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis. PLoS medicine 2016 Dec 13 (12): e1002201. Lefebvre Celine, Bachelot Thomas, Filleron Thomas, Pedrero Marion, Campone Mario, Soria Jean-Charles, Massard Christophe, Lévy Christelle, Arnedos Monica, Lacroix-Triki Magali, Garrabey Julie, Boursin Yannick, Deloger Marc, Fu Yu, Commo Frédéric, Scott Véronique, Lacroix Ludovic, Dieci Maria Vittoria, Kamal Maud, Diéras Véronique, Gonçalves Anthony, Ferrerro Jean-Marc, Romieu Gilles, Vanlemmens Laurence, Mouret Reynier Marie-Ange, Théry Jean-Christophe, Le Du Fanny, Guiu Séverine, Dalenc Florence, Clapisson Gilles, Bonnefoi Hervé, Jimenez Marta, Le Tourneau Christophe, André Fabri |
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.
Human molecular genetics 2018 Feb 27 (3): 559-575. Liu Fan, Chen Yan, Zhu Gu, Hysi Pirro G, Wu Sijie, Adhikari Kaustubh, Breslin Krystal, Pospiech Ewelina, Hamer Merel A, Peng Fuduan, Muralidharan Charanya, Acuna-Alonzo Victor, Canizales-Quinteros Samuel, Bedoya Gabriel, Gallo Carla, Poletti Giovanni, Rothhammer Francisco, Bortolini Maria Catira, Gonzalez-Jose Rolando, Zeng Changqing, Xu Shuhua, Jin Li, Uitterlinden André G, Ikram M Arfan, van Duijn Cornelia M, Nijsten Tamar, Walsh Susan, Branicki Wojciech, Wang Sijia, Ruiz-Linares Andrés, Spector Timothy D, Martin Nicholas G, Medland Sarah E, Kayser Manfr |
Patterns of Mutation Enrichment in Metastatic Triple-Negative Breast Cancer. Clinical Medicine Insights. Oncology 2019 13 1179554919868482. Saravia César H, Flores Claudio, Schwarz Luis J, Bravo Leny, Zavaleta Jenny, Araujo Jhajaira, Neciosup Silvia, Pinto Joseph |
Whole-exome sequencing identifies variants associated with structural MRI markers in patients with bipolar disorders. Journal of affective disorders 2019 Feb 249 159-168. Han Mi-Ryung, Han Kyu-Man, Kim Aram, Kang Wooyoung, Kang Youbin, Kang June, Won Eunsoo, Tae Woo-Suk, Cho Yunjung, Ham Byung-J |
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract. Journal of clinical medicine 2020 3 9 (3): . Ahn Yo Han, Lee Chung, Kim Nayoung K D, Park Eujin, Kang Hee Gyung, Ha Il-Soo, Park Woong-Yang, Cheong Hae |
A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer. The Prostate 2021 5 81 (10): 683-693. Wang Victoria, Geybels Milan S, Jordahl Kristina M, Gerke Travis, Hamid Anis, Penney Kathryn L, Markt Sarah C, Freedman Matthew, Pomerantz Mark, Lee Gwo-Shu M, Rana Huma, Börnigen Daniela, Rebbeck Timothy R, Huttenhower Curtis, Eeles Ros A, Stanford Janet L, Consortium Practical, Berndt Sonja I, Claessens Frank, Sørensen Karina D, Park Jong Y, Vega Ana, Usmani Nawaid, Mucci Lorelei, Sweeney Christopher |
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. Frontiers in genetics 2022 8 13 886038. Alaamery Manal, Alghamdi Jahad, Massadeh Salam, Alsawaji Mona, Aljawini Nora, Albesher Nour, Alghamdi Bader, Almutairi Mansour, Hejaili Fayez, Alfadhel Majid, Baz Batoul, Almuzzaini Bader, Almutairi Adel F, Abdullah Mubarak, Quintana Francisco J, Sayyari Abdull |
SLC4A4, FRAS1, and SULT1A1 Genetic Variations Associated With Dabigatran Metabolism in a Healthy Chinese Population. Frontiers in genetics 2022 6 13 873031. Xie Qiufen, Li Yuan, Liu Zhiyan, Mu Guangyan, Zhang Hanxu, Zhou Shuang, Wang Zhe, Wang Zining, Jiang Jie, Li Xin, Xiang Qian, Cui Yim |
Association of a Novel DOCK2 Mutation-Related Gene Signature With Immune in Hepatocellular Carcinoma. Frontiers in genetics 2022 13 872224. Huang Yushen, Luo Wen, Chen Siyun, Su Hongmei, Zhu Wuchang, Wei Yuanyuan, Qiu Yue, Long Yan, Shi Yanxia, Wei Jinb |
Blood and brain transcriptome analysis reveals APOE genotype-mediated and immune-related pathways involved in Alzheimer disease. Alzheimer's research & therapy 2022 2 14 (1): 30. Panitch Rebecca, Hu Junming, Xia Weiming, Bennett David A, Stein Thor D, Farrer Lindsay A, Jun Gyungah |
Novel Gene Polymorphisms for Stable Warfarin Dose in a Korean Population: Genome-Wide Association Study. Biomedicines 2023 8 11 (8): . Jung Sun Kim, Sak Lee, Jeong Yee, Kyemyung Park, Eun Jeong Jang, Byung Chul Chang, Hye Sun Gw |
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