Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 35 Records) |
| Query Trace: Disease and MC1R[original query] |
|---|
| Melanocortin receptor 1 variants and melanoma risk: a study of 2 European populations. International journal of cancer. Journal international du cancer 2009 Apr . Scherer D, Nagore E, Bermejo JL, Figl A, Botella-Estrada R, Thirumaran RK, Angelini S, Hemminki K, Schadendorf D, Kumar R |
| Role of key-regulator genes in melanoma susceptibility and pathogenesis among patients from South Italy. BMC cancer 2009 9 (1): 352. Casula Milena, Muggiano Antonio, Cossu Antonio, Budroni Mario, Caracò Corrado, Ascierto Paolo A, Pagani Elena, Stanganelli Ignazio, Canzanella Sergio, Sini Mariacristina, Palomba Grazia, , Palmieri Giusep |
| Malignant melanoma--a genetic overview. Actas dermo-sifiliograficas 2010 1 100 Suppl 1 38-51. Bloethner S, Scherer D, Drechsel M, Hemminki K, Kumar |
| ASSESSMENT OF MC1R AND a-MSH GENE SEQUENCES IN IRANIAN VITILIGO PATIENTS. Indian journal of dermatology 2010 Oct 55 (4): 325-8. Eskandani M, Hasannia S, Vandghanooni S, Pirooznia N, Golchai |
| Genotype analysis in Hungarian patients with multiple primary melanoma. Experimental dermatology 2014 May 23 (5): 361-4. Hatvani Zsófia, Brodszky Valentin, Mazán Mercédesz, Pintér Dóra, Hársing Judit, Tóth Veronika, Somlai Beáta, Kárpáti Sarol |
| The melanocortin 1 receptor (Mc1r) variants do not account for the co-occurrence of Parkinson's disease and malignant melanoma. Journal of molecular neuroscience : MN 2014 Dec 54 (4): 820-5. Elincx-Benizri Sandra, Inzelberg Rivka, Greenbaum Lior, Cohen Oren S, Yahalom Gilad, Laitman Yael, Djaldetti Ruth, Orlev Yael, Scope Alon, Azizi Esther, Friedman Eitan, Hassin-Baer Shar |
| Genetic analysis of MC1R variants in Chinese Han patients with sporadic Parkinson's disease. Neuroscience letters 2015 Nov . He Sihan, Tan Ting, Song Zhi, Yuan Lamei, Deng Xiong, Ni Bin, Chen Yong, Hao De |
| The MC1R melanoma risk variant p.R160W is associated with Parkinson disease. Annals of neurology 2015 May 77 (5): 889-94. Tell-Marti Gemma, Puig-Butille Joan Anton, Potrony Miriam, Badenas Celia, Milà Montserrat, Malvehy Josep, Martí María José, Ezquerra Mario, Fernández-Santiago Rubén, Puig Susa |
| Pigmentation-Independent Susceptibility Loci for Actinic Keratosis Highlighted by Compound Heterozygosity Analysis. The Journal of investigative dermatology 2016 Sep . Zhong Kaiyin, Verkouteren Joris A C, Jacobs Leonie C, Uitterlinden Andre G, Hofman A, Liu Fan, Nijsten Tamar, Kayser Manfr |
| The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder. Neurobiology of aging 2016 Apr . Gan-Or Ziv, Mohsin Noreen, Girard Simon L, Montplaisir Jacques Y, Ambalavanan Amirthagowri, Strong Stephanie, Mallett Victoria, Laurent Sandra B, Bourassa Cynthia V, Boivin Michel, Langlois Melanie, Arnulf Isabelle, Högl Birgit, Frauscher Birgit, Monaca Christelle, Desautels Alex, Gagnon Jean-François, Postuma Ronald B, Dion Patrick A, Dauvilliers Yves, Dupre Nicolas, Alcalay Roy N, Rouleau Guy |
| MC1R variants in Chinese Han patients with sporadic Parkinson's disease. Neurobiology of aging 2016 Mar . Shi Chang-He, Wang Hui, Mao Cheng-Yuan, Yang Jing, Song Bo, Liu Yu-Tao, Yang Zhi-Hua, Luo Hai-Yang, Zhang Shu-Yu, Wu Jun, Xu Yu-Mi |
| The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients. Molecular neurobiology 2016 Dec . Tell-Marti Gemma, Puig-Butille Joan Anton, Gimenez-Xavier Pol, Segu-Roig Ariadna, Potrony Miriam, Badenas Celia, Alvarez Victoria, Millán José M, Trujillo-Tiebas María José, Ramos-Arroyo María A, Milà Montserrat, Puig Susa |
| Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF. The British journal of dermatology 2016 Jul . Mangas C, Potrony M, Mainetti C, Bianchi E, Carrozza Merlani P, Mancarella Eberhardt A, Maspoli-Postizzi E, Marazza G, Marcollo-Pini A, Pelloni F, Sessa C, Simona B, Puig-Butillé J A, Badenas C, Puig |
| Characterization of patients at high risk of melanoma in Austria. The British journal of dermatology 2016 Jan . Müller C, Wendt J, Rauscher S, Burgstaller-Muehlbacher S, Sunder-Plassmann R, Scheurecker C, Richtig E, Fae I, Fischer G, Pehamberger H, Okamoto |
| Genetic modifiers of multiple sclerosis progression, severity and onset. Clinical immunology (Orlando, Fla.) 2017 May 180 100-105. Sadovnick A Dessa, Traboulsee Anthony L, Zhao Yinshan, Bernales Cecily Q, Encarnacion Mary, Ross Jay P, Yee Irene M, Criscuoli Maria G, Vilariño-Güell Carl |
| Clinical and genetic characteristics of xeroderma pigmentosum in Nepal. Journal of the European Academy of Dermatology and Venereology : JEADV 2017 11 32 (5): 832-839. Espi P, Parajuli S, Benfodda M, Lebre A-S, Paudel U, Grange A, Grybek V, Grange T, Soufir N, Grange |
| A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk. Journal of Alzheimer's disease : JAD 2017 Dec . Tell-Marti Gemma, Puig-Butille Joan Anton, Potrony Miriam, Plana Estel, Badenas Celia, Antonell Anna, Sanchez-Valle Raquel, Molinuevo José L, Lleó Alberto, Alcolea Daniel, Fortea Juan, Fernández-Santiago Rubén, Clarimón Jordi, Lladó Albert, Puig Susa |
| Systematic analysis of genetic variants in patients with essential tremor. Brain and behavior 2018 10 8 (10): e01100. Yuan Lamei, Deng Xiong, Song Zhi, Deng Sheng, Zheng Wen, Mao Ping, Deng H |
| Bioluminescent SNP genotyping technique: Development and application for detection of melanocortin 1 receptor gene polymorphisms. Talanta 2018 Nov 189 111-115. Bashmakova Eugenia E, Krasitskaya Vasilisa V, Bondar Alexander A, Eremina Ekaterina N, Slepov Eugene V, Zukov Ruslan A, Frank Ludmila |
| Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels. PloS one 2018 13 (3): e0193893. Nair-Shalliker Visalini, Egger Sam, Chrzanowska Agata, Mason Rebecca, Waite Louise, Le Couteur David, Seibel Markus J, Handelsman David J, Cumming Robert, Smith David P, Armstrong Bruce |
| Integrated case-control and somatic-germline interaction analyses of melanoma susceptibility genes. Biochimica et biophysica acta. Molecular basis of disease 2018 Jun 1864 (6 Pt B): 2247-2254. Yu Yao, Hu Hao, Chen Jiun-Sheng, Hu Fulan, Fowler Jerry, Scheet Paul, Zhao Hua, Huff Chad |
| Does the gene matter? Genotype-phenotype and genotype-outcome associations in congenital melanocytic naevi. The British journal of dermatology 2019 5 182 (2): 434-443. Polubothu S, McGuire N, Al-Olabi L, Baird W, Bulstrode N, Chalker J, Josifova D, Lomas D, O'Hara J, Ong J, Rampling D, Stadnik P, Thomas A, Wedgeworth E, Sebire N J, Kinsler V |
| A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for ocular squamous cell carcinoma in Belgian horses. Equine veterinary journal 2019 Mar . Knickelbein K E, Lassaline M E, Singer-Berk M, Reilly C M, Clode A B, Famula T R, Michau T M, Bellone R |
| Functional annotation of melanoma risk loci identifies novel susceptibility genes. Carcinogenesis 2019 Oct . Fang Shenying, Lu Jiachun, Zhou Xinke, Wang Yuling, Ross Merrick I, Gershenwald Jeffrey E, Cormier Janice N, Wargo Jennifer, Sui Dawen, Amos Christopher I, Lee Jeffrey |
| Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients. Journal of the European Academy of Dermatology and Venereology : JEADV 2019 Jan . Rayner J E, McMeniman E K, Duffy D L, De'Ambrosis B, Smithers B M, Jagirdar K, Lee K J, Soyer H P, Sturm R |
| A Robust Prognostic Gene Signature Based on eRNAs-Driven Genes in Prostate Cancer. Frontiers in genetics 2021 7 12 676845. Fan Shuaishuai, Wang Zheng, Zhao Li, Zhao ChenHui, Yuan DaJiang, Wang Jing |
| Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development. Frontiers in neuroscience 2022 4 16 817713. Kolarikova Kristyna, Vodicka Radek, Vrtel Radek, Stellmachova Julia, Prochazka Martin, Mensikova Katerina, Kanovsky Pe |
| NGS-based targeted sequencing identified two novel variants in Southwestern Chinese families with oculocutaneous albinism. BMC genomics 2022 4 23 (1): 332. Xiao Yuanyuan, Zhou Cong, Xie Hanbing, Huang Shuang, Wang Jing, Liu Shanli |
Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes.
BMC genomics 2022 12 23 (1): 840. Vollenbrock Charlotte E, Roshandel Delnaz, van der Klauw Melanie M, Wolffenbuttel Bruce H R, Paterson Andrew |
| Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort.
Genes 2023 1 14 (1): . Farré Xavier, Blay Natalia, Cortés Beatriz, Carreras Anna, Iraola-Guzmán Susana, de Cid Rafa |
- Page last reviewed:Feb 1, 2024
- Content source: