Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: RASA1[original query] |
---|
Meta-analysis of genome-wide association studies for personality.
Molecular psychiatry 2012 Mar 17 (3): 337-49. de Moor M H M, Costa P T, Terracciano A, Krueger R F, de Geus E J C, Toshiko T, Penninx B W J H, Esko T, Madden P A F, Derringer J, Amin N, Willemsen G, Hottenga J-J, Distel M A, Uda M, Sanna S, Spinhoven P, Hartman C A, Sullivan P, Realo A, Allik J, Heath A C, Pergadia M L, Agrawal A, Lin P, Grucza R, Nutile T, Ciullo M, Rujescu D, Giegling I, Konte B, Widen E, Cousminer D L, Eriksson J G, Palotie A, Peltonen L, Luciano M, Tenesa A, Davies G, Lopez L M, Hansell N K, Medland S E, Ferrucci L, Schlessinger D, Montgomery G W, Wright M J, Aulchenko Y S, Janssens A C J W, Oostra B A, Metspalu A, Abecasis G R, Deary I J, Räikkönen K, Bierut L J, Martin N G, van Duijn C M, Boomsma D |
Mutational landscape of aggressive cutaneous squamous cell carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Dec 20 (24): 6582-92. Pickering Curtis R, Zhou Jane H, Lee J Jack, Drummond Jennifer A, Peng S Andrew, Saade Rami E, Tsai Kenneth Y, Curry Jonathan L, Tetzlaff Michael T, Lai Stephen Y, Yu Jun, Muzny Donna M, Doddapaneni Harshavardhan, Shinbrot Eve, Covington Kyle R, Zhang Jianhua, Seth Sahil, Caulin Carlos, Clayman Gary L, El-Naggar Adel K, Gibbs Richard A, Weber Randal S, Myers Jeffrey N, Wheeler David A, Frederick Mitchell |
Next-Generation Sequencing of Pulmonary Sarcomatoid Carcinoma Reveals High Frequency of Actionable MET Gene Mutations. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015 Jul . Liu Xuewen, Jia Yuxia, Stoopler Mark B, Shen Yufeng, Cheng Haiying, Chen Jinli, Mansukhani Mahesh, Koul Sanjay, Halmos Balazs, Borczuk Alain |
Genetic Variants Associated with Port-Wine Stains. PloS one 2015 10 (7): e0133158. Frigerio Alice, Wright Karol, Wooderchak-Donahue Whitney, Tan Oon T, Margraf Rebecca, Stevenson David A, Grimmer J Fredrik, Bayrak-Toydemir Pin |
Two susceptibility loci identified for prostate cancer aggressiveness.
Nature communications 2015 6 6889. Berndt Sonja I, Wang Zhaoming, Yeager Meredith, Alavanja Michael C, Albanes Demetrius, Amundadottir Laufey, Andriole Gerald, Beane Freeman Laura, Campa Daniele, Cancel-Tassin Geraldine, Canzian Federico, Cornu Jean-Nicolas, Cussenot Olivier, Diver W Ryan, Gapstur Susan M, Grönberg Henrik, Haiman Christopher A, Henderson Brian, Hutchinson Amy, Hunter David J, Key Timothy J, Kolb Suzanne, Koutros Stella, Kraft Peter, Le Marchand Loic, Lindström Sara, Machiela Mitchell J, Ostrander Elaine A, Riboli Elio, Schumacher Fred, Siddiq Afshan, Stanford Janet L, Stevens Victoria L, Travis Ruth C, Tsilidis Konstantinos K, Virtamo Jarmo, Weinstein Stephanie, Wilkund Fredrik, Xu Jianfeng, Lilly Zheng S, Yu Kai, Wheeler William, Zhang Han, , Sampson Joshua, Black Amanda, Jacobs Kevin, Hoover Robert N, Tucker Margaret, Chanock Stephen |
Identification of the BRAF V600E mutation in gastroenteropancreatic neuroendocrine tumors. Oncotarget 2015 Dec . Park Charny, Ha Sang Yun, Kim Seung Tae, Kim Hee Cheol, Heo Jin Seok, Park Young Suk, Lauwers Gregory, Lee Jeeyun, Kim Kyoung-M |
Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas. Nature genetics 2016 May . Campbell Joshua D, Alexandrov Anton, Kim Jaegil, Wala Jeremiah, Berger Alice H, Pedamallu Chandra Sekhar, Shukla Sachet A, Guo Guangwu, Brooks Angela N, Murray Bradley A, Imielinski Marcin, Hu Xin, Ling Shiyun, Akbani Rehan, Rosenberg Mara, Cibulskis Carrie, Ramachandran Aruna, Collisson Eric A, Kwiatkowski David J, Lawrence Michael S, Weinstein John N, Verhaak Roel G W, Wu Catherine J, Hammerman Peter S, Cherniack Andrew D, Getz Gad, , Artyomov Maxim N, Schreiber Robert, Govindan Ramaswamy, Meyerson Matth |
Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia. Human genome variation 2016 4 2 15040. Hernandez Felicia, Huether Robert, Carter Lester, Johnston Tami, Thompson Jennifer, Gossage James R, Chao Elizabeth, Elliott Aaron |
Integrated analysis of oral tongue squamous cell carcinoma identifies key variants and pathways linked to risk habits, HPV, clinical parameters and tumor recurrence. F1000Research 2015 4 1215. Krishnan Neeraja, Gupta Saurabh, Palve Vinayak, Varghese Linu, Pattnaik Swetansu, Jain Prach, Khyriem Costerwell, Hariharan Arun, Dhas Kunal, Nair Jayalakshmi, Pareek Manisha, Prasad Venkatesh, Siddappa Gangotri, Suresh Amritha, Kekatpure Vikram, Kuriakose Moni, Panda Bin |
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE. Acta dermato-venereologica 2017 11 98 (2): 251-255. Maruani Annabel, Durieux-Verde Marine, Mazereeuw-Hautier Juliette, Boccara Olivia, Martin Ludovic, Chiaverini Christine, Eschard Catherine, Bénéton Nathalie, Vabres Pierre, Balguerie Xavier, Plantin Patrice, Bessis Didier, Barbarot Sébastien, Dadban Ali, Droitcourt Catherine, Berthelot Aline, Lorette Gérard, Leducq Sophie, Samimi Mahtab, Andres Christian, Caille Agnès, Vourc'h Patrick, |
Clinical and genetic findings in children with central nervous system arteriovenous fistulas. Annals of neurology 2017 11 82 (6): 972-980. Saliou Guillaume, Eyries Mélanie, Iacobucci Marta, Knebel Jean-François, Waill Marie-Christine, Coulet Florence, Ozanne Augustin, Soubrier Flore |
RASA1 and NF1 are Preferentially Co-Mutated and Define A Distinct Genetic Subset of Smoking-Associated Non-Small Cell Lung Carcinomas Sensitive to MEK Inhibition. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Nov . Hayashi Takuo, Desmeules Patrice, Smith Roger S, Drilon Alexander, Somwar Romel, Ladanyi Ma |
RASA1/NF1-Mutant Lung Cancer: Racing to the Clinic? Clinical cancer research : an official journal of the American Association for Cancer Research 2018 1 24 (6): 1243-1245. Kitajima Shunsuke, Barbie David |
RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation. Journal of medical genetics 2019 7 57 (1): 48-52. Revencu Nicole, Fastre Elodie, Ravoet Marie, Helaers Raphaël, Brouillard Pascal, Bisdorff-Bresson Annouk, Chung Clara W T, Gerard Marion, Dvorakova Veronika, Irvine Alan D, Boon Laurence M, Vikkula Miik |
Radiogenomics of rectal adenocarcinoma in the era of precision medicine: A pilot study of associations between qualitative and quantitative MRI imaging features and genetic mutations. European journal of radiology 2019 Apr 113 174-181. Horvat Natally, Veeraraghavan Harini, Pelossof Raphael A, Fernandes Maria Clara, Arora Arshi, Khan Monika, Marco Michael, Cheng Chin-Tung, Gonen Mithat, Golia Pernicka Jennifer S, Gollub Marc J, Garcia-Aguillar Julio, Petkovska I |
Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)? Genetics in medicine : official journal of the American College of Medical Genetics 2019 Feb . Wooderchak-Donahue Whitney L, Akay Gulsen, Whitehead Kevin, Briggs Eric, Stevenson David A, O'Fallon Brendan, Velinder Matthew, Farrell Andrew, Shen Wei, Bedoukian Emma, Skrabann Cara M, Antaya Richard J, Henderson Kate, Pollak Jeffrey, Treat James, Day Ronald, Jacher Joseph E, Hannibal Mark, Bontempo Kelly, Marth Gabor, Bayrak-Toydemir Pinar, McDonald Jam |
Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases. Genes, chromosomes & cancer 2019 1 58 (8): 541-550. Ten Broek Roel W, Eijkelenboom Astrid, van der Vleuten Carine J M, Kamping Eveline J, Kets Marleen, Verhoeven Bas H, Grünberg Katrien, Schultze Kool Leo J, Tops Bastiaan B J, Ligtenberg Marjolijn J L, Flucke U |
Mutational signatures and the genomic landscape of betel quid chewing-associated tongue carcinoma. Cancer medicine 2019 1 8 (2): 701-711. Zhang Weilong, Wang Mu, Wu Qifeng, Zhu Qing, Jiao Yuchen, Zhu Yiming, Yang Beibei, Ni Song, Yu Jianjun, Sun Hong, Zeng Yi-X |
Capillary malformation-arteriovenous malformation syndrome: a multicentre study. Clinical and experimental dermatology 2020 8 46 (2): 300-305. Valdivielso-Ramos M, Martin-Santiago A, Azaña J M, Hernández-Nuñez A, Vera A, Perez B, Tercedor J, Feito M, Vicente A, Prat C, Lopez-Gutierrez J C, Garnacho G, Baselga E, Roe E, Palencia S, Cordero P, Moreno R, Agudo A, de la Cueva P, Torrelo |
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation. Molecular genetics & genomic medicine 2021 Sep e1794. Choksi Foram, Weinsheimer Shantel, Nelson Jeffrey, Pawlikowska Ludmila, Fox Christine K, Zafar Atif, Mabray Marc C, Zabramski Joseph, Akers Amy, Hart Blaine L, Morrison Leslie, McCulloch Charles E, Kim Hel |
Coexistence of RASA1 and COL4A2 variants caused pial arteriovenous fistula (AVF) in a patient with capillary malformation-arteriovenous malformation. Clinical neurology and neurosurgery 2021 4 204 106612. Kumai Tadashi, Sadato Akiyo, Kurahashi Hiroki, Kato Takema, Adachi Kazuhide, Hirose Yuic |
[Clinical phenotype and genetic analysis of a case of 5q14.3 microdeletion syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 11 38 (11): 1127-1131. Xu Xin, Li Hongying, Zhang Li, Lu Fen, Tang Ji |
Prognostic features and comprehensive genomic analysis of NF1 mutations in EGFR mutant lung cancer patients. Cancer medicine 2022 Jun . Tian Hong-Xia, Chen Zhi-Hong, Jie Guang-Ling, Wang Zhen, Yan Hong-Hong, Wu Si-Pei, Zhang Shui-Lian, Lu Dan-Xia, Zhang Xu-Chao, Wu Yi-Lo |
Arteriovenous Cerebral High Flow Shunts in Children: From Genotype to Phenotype. Frontiers in pediatrics 2022 5 10 871565. Tas Berivan, Starnoni Daniele, Smajda Stanislas, Vivanti Alexandre J, Adamsbaum Catherine, Eyries Mélanie, Melki Judith, Tawk Marcel, Ozanne Augustin, Revencu Nicole, Soubrier Florent, Siala Selima, Vikkula Miikka, Deiva Kumaran, Saliou Guillau |
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants. Journal of medical genetics 2022 3 60 (2): 163-173. Mussa Alessandro, Leoni Chiara, Iacoviello Matteo, Carli Diana, Ranieri Carlotta, Pantaleo Antonino, Buonuomo Paola Sabrina, Bagnulo Rosanna, Ferrero Giovanni Battista, Bartuli Andrea, Melis Daniela, Maitz Silvia, Loconte Daria Carmela, Turchiano Antonella, Piglionica Marilidia, De Luisi Annunziata, Susca Francesco Claudio, Bukvic Nenad, Forleo Cinzia, Selicorni Angelo, Zampino Giuseppe, Onesimo Roberta, Cappuccio Gerarda, Garavelli Livia, Novelli Chiara, Memo Luigi, Morando Carla, Della Monica Matteo, Accadia Maria, Capurso Martina, Piscopo Carmelo, Cereda Anna, Di Giacomo Marilena Carmela, Saletti Veronica, Spinelli Alessandro Mauro, Lastella Patrizia, Tenconi Romano, Dvorakova Veronika, Irvine Alan D, Resta Nicolet |
Somatic mutational landscape of extracranial arteriovenous malformations and phenotypic correlations. Journal of the European Academy of Dermatology and Venereology : JEADV 2022 3 36 (6): 905-912. El Sissy F N, Wassef M, Faucon B, Salvan D, Nadaud S, Coulet F, Adle-Biassette H, Soubrier F, Bisdorff A, Eyries |
Mutational spectrum of syndromic genes in sporadic brain arteriovenous malformation. Chinese neurosurgical journal 2022 2 8 (1): 4. Wang Kun, Zhang Mingqi, Zhao Sen, Xie Zhixin, Zhang Yisen, Liu Jian, Zhang Ying, Yang Xinjian, Wu N |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: