Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 44 Records) |
Query Trace: EDAR[original query] |
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Mutations in EDA and EDAR Genes in a Large Mexican Hispanic Cohort with Hypohidrotic Ectodermal Dysplasia. Annals of dermatology 2015 Aug 27 (4): 474-7. Salas-Alanis Julio C, Wozniak Eva, Mein Charles A, Duran Mckinster Carola C, Ocampo-Candiani Jorge, Kelsell David P, Hua Rong, Garza-Rodriguez Maria L, Choate Keith A, Barrera Saldaña Hugo |
Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients. Genes 2016 7 (9): . Zeng Binghui, Xiao Xue, Li Sijie, Lu Hui, Lu Jiaxuan, Zhu Ling, Yu Dongsheng, Zhao W |
Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations.
Human genetics 2016 Nov 135 (11): 1279-1286. Wu Sijie, Tan Jingze, Yang Yajun, Peng Qianqian, Zhang Manfei, Li Jinxi, Lu Dongsheng, Liu Yu, Lou Haiyi, Feng Qidi, Lu Yan, Guan Yaqun, Zhang Zhaoxia, Jiao Yi, Sabeti Pardis, Krutmann Jean, Tang Kun, Jin Li, Xu Shuhua, Wang Sij |
Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis. European journal of medical genetics 2016 Jun 59 (8): 377-385. Shahid Mohammad, Balto Hanan A, Al-Hammad Nouf, Joshi S, Khalil Hesham Saleh, Somily Ali Mohammed, Sinjilawi Nasr Abdul-Aziz, Al-Ghamdi Sameer, Faiyaz-Ul-Haque Muhammad, Dhillon Varinderpal |
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.
Nature communications 2016 May 7 11616. Adhikari Kaustubh, Fuentes-Guajardo Macarena, Quinto-Sánchez Mirsha, Mendoza-Revilla Javier, Camilo Chacón-Duque Juan, Acuña-Alonzo Victor, Jaramillo Claudia, Arias William, Lozano Rodrigo Barquera, Pérez Gastón Macín, Gómez-Valdés Jorge, Villamil-Ramírez Hugo, Hunemeier Tábita, Ramallo Virginia, Silva de Cerqueira Caio C, Hurtado Malena, Villegas Valeria, Granja Vanessa, Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Salzano Francisco M, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Cheeseman Michael, Rosique Javier, Bedoya Gabriel, Rothhammer Francisco, Headon Denis, González-José Rolando, Balding David, Ruiz-Linares Andr |
Atlas of human diseases influenced by genetic variants with extreme allele frequency differences. Human genetics 2016 Oct . Sulovari Arvis, Chen Yolanda H, Hudziak James J, Li Daw |
Downstream activation of NF-?B in the EDA-A1/EDAR signalling in Sjögren's syndrome and its regulation by the ubiquitin-editing enzyme A20. Clinical and experimental immunology 2016 Jan . Sisto Margherita, Barca Amilcare, Lofrumento Dario Domenico, Lisi Sabri |
Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population. The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association (CSA) 2017 20 (3): 153-159. Chen Yi Ting, Liu Hao Chen, Han Dong, Liu Yang, Feng Hai L |
Evolutionary significance of selected EDAR variants in Tibetan high-altitude adaptations. Science China. Life sciences 2017 8 61 (1): 68-78. Shao Jianming, Raza Muhammad Sohail, Zhuoma Basang, Zeng Changqi |
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 |
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
American journal of human genetics 2017 Dec 101 (6): 913-924. Shaffer John R, Li Jinxi, Lee Myoung Keun, Roosenboom Jasmien, Orlova Ekaterina, Adhikari Kaustabh, , Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Rothhammer Francisco, Bedoya Gabriel, González-José Rolando, Pfeffer Paige E, Wollenschlaeger Christopher A, Hecht Jacqueline T, Wehby George L, Moreno Lina M, Ding Anan, Jin Li, Yang Yajun, Carlson Jenna C, Leslie Elizabeth J, Feingold Eleanor, Marazita Mary L, Hinds David A, Cox Timothy C, Wang Sijia, Ruiz-Linares Andrés, Weinberg Seth |
Geographic Variation in EGFR Mutation Frequency in Lung Adenocarcinoma May Be Explained by Interethnic Genetic Variation. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2018 03 13 (3): 454-458. Soraas Lars, Stebbing Just |
Relation of Odor Identification with Alzheimer's Disease Markers in Cerebrospinal Fluid and Cognition. Journal of Alzheimer's disease : JAD 2017 60 (3): 1025-1034. Reijs Babette L R, Ramakers Inez H G B, Elias-Sonnenschein Lyzel, Teunissen Charlotte E, Koel-Simmelink Marleen, Tsolaki Magda, Wahlund Lars-Olof, Waldemar Gunhild, Hausner Lucrezia, Johannsen Peter, Vanderstichele Hugo, Verhey Frans, Devanand D P, Visser Pieter Jel |
WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI). Clinical genetics 2017 Oct . Guazzarotti L, Tadini G, Mancini G E, Sani I, Pisanelli S, Galderisi F, D'Auria E, Secondi R, Bottero A, Zuccotti G |
Mutational spectrum of EDA and EDAR genes in a cohort of Mexican mestizo patients with hypohidrotic ectodermal dysplasia. Journal of the European Academy of Dermatology and Venereology : JEADV 2017 1 31 (7): e321-e324. Monroy-Jaramillo N, Abad-Flores J D, García-Delgado C, Villaseñor-Domínguez A, Mena-Cedillos C, Toledo-Bahena M E, Valencia-Herrera A M, Sánchez-Boiso A, Akaki-Carreño Y I, Del Río Navarro B, Aguirre-Hernández J, López-López M, Cervantes A, Cerbón M, Morán-Barroso V |
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans.
PLoS genetics 2018 09 14 (9): e1007640. Wu Sijie, Zhang Manfei, Yang Xinzhou, Peng Fuduan, Zhang Juan, Tan Jingze, Yang Yajun, Wang Lina, Hu Yanan, Peng Qianqian, Li Jinxi, Liu Yu, Guan Yaqun, Chen Chen, Hamer Merel A, Nijsten Tamar, Zeng Changqing, Adhikari Kaustubh, Gallo Carla, Poletti Giovanni, Schuler-Faccini Lavinia, Bortolini Maria-Cátira, Canizales-Quinteros Samuel, Rothhammer Francisco, Bedoya Gabriel, González-José Rolando, Li Hui, Krutmann Jean, Liu Fan, Kayser Manfred, Ruiz-Linares Andres, Tang Kun, Xu Shuhua, Zhang Liang, Jin Li, Wang Sij |
Divergent genetic mechanism leads to spiny hair in rodents. PloS one 2018 8 13 (8): e0202219. Gonçalves Gislene L, Maestri Renan, Moreira Gilson R P, Jacobi Marly A M, Freitas Thales R O, Hoekstra Hopi |
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Scientific reports 2018 Jun 8 (1): 8974. Endo Chihiro, Johnson Todd A, Morino Ryoko, Nakazono Kazuyuki, Kamitsuji Shigeo, Akita Masanori, Kawajiri Maiko, Yamasaki Tatsuya, Kami Azusa, Hoshi Yuria, Tada Asami, Ishikawa Kenichi, Hine Maaya, Kobayashi Miki, Kurume Nami, Tsunemi Yuichiro, Kamatani Naoyuki, Kawashima Mako |
[The effect of EDARV370A on facial and ear morphologies in Uyghur population]. Yi chuan = Hereditas 2018 Nov 40 (11): 1024-1032. Li Yi, Zhao Wen Ting, Li Dan, Tao Xian Ming, Xiong Zi Yi, Liu Jing, Zhang Wei, Liu Hai Bo, Ji An Quan, Tang Kun, Liu Fan, Li Cai X |
Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA. Forensic science international. Genetics 2018 10 37 241-251. Po?piech Ewelina, Chen Yan, Kukla-Bartoszek Magdalena, Breslin Krystal, Aliferi Anastasia, Andersen Jeppe D, Ballard David, Chaitanya Lakshmi, Freire-Aradas Ana, van der Gaag Kristiaan J, Girón-Santamaría Lorena, Gross Theresa E, Gysi Mario, Huber Gabriela, Mosquera-Miguel Ana, Muralidharan Charanya, Skowron Ma?gorzata, Carracedo Ángel, Haas Cordula, Morling Niels, Parson Walther, Phillips Christopher, Schneider Peter M, Sijen Titia, Syndercombe-Court Denise, Vennemann Marielle, Wu Sijie, Xu Shuhua, Jin Li, Wang Sijia, Zhu Ghu, Martin Nick G, Medland Sarah E, Branicki Wojciech, Walsh Susan, Liu Fan, Kayser Manfred, |
WNT10B mutations associated with isolated dental anomalies. Clinical genetics 2018 1 93 (5): 992-999. Kantaputra P N, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns J |
Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families. Cytogenetic and genome research 2019 4 157 (4): 189-196. Güven Yeliz, Bal Elodie, Altunoglu Umut, Yücel Esra, Hadj-Rabia Smail, Koruyucu Mine, Bahar Tuna Elif, Ç?ld?r ?ule, Aktören Oya, Bodemer Christine, Uyguner Zehra O, Smahi Asma, Kayserili Hül |
Editors' Note to: EDAR, LYPLAL1, PRDM16, PAX3, DKK1, TNFSF12, CACNA2D3, and SUPT3H gene variants influence facial morphology in a Eurasian population. Human genetics 2019 Dec . Authors are not available |
EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population. Orphanet journal of rare diseases 2019 12 14 (1): 281. Martínez-Romero María Carmen, Ballesta-Martínez María Juliana, López-González Vanesa, Sánchez-Soler María José, Serrano-Antón Ana Teresa, Barreda-Sánchez María, Rodriguez-Peña Lidya, Martínez-Menchon María Teresa, Frías-Iniesta José, Sánchez-Pedreño Paloma, Carbonell-Meseguer Pablo, Glover-López Guillermo, Guillén-Navarro Encarna, |
Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia. Human mutation 2020 9 41 (11): 1957-1966. Zhang Liutao, Yu Miao, Wong Sing-Wai, Qu Hong, Cai Tao, Liu Yang, Liu Haochen, Fan Zhuangzhuang, Zheng Jinglei, Zhou Yongsheng, Feng Hailan, Han Do |
Retraction Note: EDAR, LYPLAL1, PRDM16, PAX3, DKK1, TNFSF12, CACNA2D3, and SUPT3H gene variants influence facial morphology in a Eurasian population. Human genetics 2021 8 140 (10): 1499. Li Yi, Zhao Wenting, Li Dan, Tao Xianming, Xiong Ziyi, Liu Jing, Zhang Wei, Ji Anquan, Tang Kun, Liu Fan, Li Caix |
A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family. Molecular genetics & genomic medicine 2021 5 9 (6): e1684. Zhang Hongyu, Kong Xuanting, Ren Jiabao, Yuan Shuo, Liu Chunyan, Hou Yan, Liu Ye, Meng Lingqiang, Zhang Guozhong, Du Qingqing, Shen Wenji |
Analyses of oligodontia phenotypes and genetic etiologies. International journal of oral science 2021 10 13 (1): 32. Zhou Mengqi, Zhang Hong, Camhi Heather, Seymen Figen, Koruyucu Mine, Kasimoglu Yelda, Kim Jung-Wook, Kim-Berman Hera, Yuson Ninna M R, Benke Paul J, Wu Yiqun, Wang Feng, Zhu Yaqin, Simmer James P, Hu Jan C |
A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.
Journal of genetics and genomics = Yi chuan xue bao 2021 2 48 (3): 198-207. Huang Yin, Li Dan, Qiao Lu, Liu Yu, Peng Qianqian, Wu Sijie, Zhang Manfei, Yang Yajun, Tan Jingze, Xu Shuhua, Jin Li, Wang Sijia, Tang Kun, Grünewald Stef |
A new variant of the ectodysplasin A receptor death domain gene associated with anhidrotic ectodermal dysplasia in a Turkish family and its simple diagnosis by restriction fragment length polymorphism. Genes & genetic systems 2023 9 . Eyyup Rencuzogullari, Banu Guven Ez |
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- Page last updated:Apr 22, 2024
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