Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: HYDIN[original query] |
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Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
PLoS genetics 2011 Jun 7 (6): e1002108. Reiner Alexander P, Lettre Guillaume, Nalls Michael A, Ganesh Santhi K, Mathias Rasika, Austin Melissa A, Dean Eric, Arepalli Sampath, Britton Angela, Chen Zhao, Couper David, Curb J David, Eaton Charles B, Fornage Myriam, Grant Struan F A, Harris Tamara B, Hernandez Dena, Kamatini Naoyuki, Keating Brendan J, Kubo Michiaki, LaCroix Andrea, Lange Leslie A, Liu Simin, Lohman Kurt, Meng Yan, Mohler Emile R, Musani Solomon, Nakamura Yusuke, O'Donnell Christopher J, Okada Yukinori, Palmer Cameron D, Papanicolaou George J, Patel Kushang V, Singleton Andrew B, Takahashi Atsushi, Tang Hua, Taylor Herman A, Taylor Kent, Thomson Cynthia, Yanek Lisa R, Yang Lingyao, Ziv Elad, Zonderman Alan B, Folsom Aaron R, Evans Michele K, Liu Yongmei, Becker Diane M, Snively Beverly M, Wilson James |
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. The European respiratory journal 2014 Dec 44 (6): 1579-88. Raidt Johanna, Wallmeier Julia, Hjeij Rim, Onnebrink Jörg Große, Pennekamp Petra, Loges Niki T, Olbrich Heike, Häffner Karsten, Dougherty Gerard W, Omran Heymut, Werner Claudi |
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate. Neurogenetics 2015 Jan 16 (1): 55-64. Quadri Marialuisa, Yang Xu, Cossu Giovanni, Olgiati Simone, Saddi Valeria M, Breedveld Guido J, Ouyang Limei, Hu Jingchu, Xu Na, Graafland Josja, Ricchi Valeria, Murgia Daniela, Guedes Leonor Correia, Mariani Claudio, Marti Maria J, Tarantino Patrizia, Asselta Rosanna, Valldeoriola Francesc, Gagliardi Monica, Pezzoli Gianni, Ezquerra Mario, Quattrone Aldo, Ferreira Joaquim, Annesi Grazia, Goldwurm Stefano, Tolosa Eduardo, Oostra Ben A, Melis Maurizio, Wang Jun, Bonifati Vincen |
Whole-Exome Sequencing Identifies Novel Somatic Mutations in Chinese Breast Cancer Patients. Journal of molecular and genetic medicine : an international journal of biomedical research 2015 Dec 9 (4): . Zhang Yanfeng, Cai Qiuyin, Shu Xiao-Ou, Gao Yu-Tang, Li Chun, Zheng Wei, Long Jiro |
Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES). Medical science monitor : international medical journal of experimental and clinical research 2018 Mar 24 1340-1358. Liu Yong, Cao Yu, Li Yaxiong, Lei Dongyun, Li Lin, Hou Zong Liu, Han Shen, Meng Mingyao, Shi Jianlin, Zhang Yayong, Wang Yi, Niu Zhaoyi, Xie Yanhua, Xiao Benshan, Wang Yuanfei, Li Xiao, Yang Lirong, Wang Wenju, Jiang Liho |
Diagnostic yield of a targeted gene panel in primary ciliary dyskinesia patients. Human mutation 2018 1 39 (5): 653-665. Paff Tamara, Kooi Irsan E, Moutaouakil Youssef, Riesebos Elise, Sistermans Erik A, Daniels Hans J M A, Weiss Janneke M M, Niessen Hans H W M, Haarman Eric G, Pals Gerard, Micha Dimit |
Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey. Pediatric pulmonology 2019 11 55 (2): 383-393. Emiralio?lu Nagehan, Ta?k?ran Ekim Z, Ko?ukcu Can, Bilgiç Elif, Atilla Pergin, Kaya Bengisu, Günayd?n Önder, Yüzba??o?lu Ay?e, Tu?cu Gökçen Dil?a, Ademhan Dilber, Ery?lmaz Polat Sanem, Gharibzadeh H?zal Mina, Yalç?n Ebru, Do?ru Deniz, Kiper Nural, Alika?ifo?lu Mehmet, Özçelik U? |
Genetic architecture of laterality defects revealed by whole exome sequencing. European journal of human genetics : EJHG 2019 1 27 (4): 563-573. Li Alexander H, Hanchard Neil A, Azamian Mahshid, D'Alessandro Lisa C A, Coban-Akdemir Zeynep, Lopez Keila N, Hall Nancy J, Dickerson Heather, Nicosia Annarita, Fernbach Susan, Boone Philip M, Gambin Tomaz, Karaca Ender, Gu Shen, Yuan Bo, Jhangiani Shalini N, Doddapaneni HarshaVardhan, Hu Jianhong, Dinh Huyen, Jayaseelan Joy, Muzny Donna, Lalani Seema, Towbin Jeffrey, Penny Daniel, Fraser Charles, Martin James, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Ware Stephanie M, Belmont John |
Clinical and Genetic Spectrum of Children with Primary Ciliary Dyskinesia in China. The Journal of pediatrics 2020 6 225 157-165.e5. Guo Zhuoyao, Chen Weicheng, Wang Libo, Qian Lili |
A Four-Gene-Based Risk Score With High Prognostic Value in Gastric Cancer. Frontiers in oncology 2021 11 584213. Zhang Bingdong, Li Yuerui, Yang Liu, Chen Yongbi |
The Relationship between Genotype and Phenotype in Primary Ciliary Dyskinesia Patients. Sisli Etfal Hastanesi tip bulteni 2021 55 (2): 188-192. Kilinc Ayse Ayzit, Cebi Memnune Nur, Ocak Zeynep, Cokugras Haluk Cez |
Clinicopathological and Molecular Analysis of 45 Cases of Pure Mucinous Breast Cancer. Frontiers in oncology 2021 3 10 558760. Yim Hyun Ee, Kim Jang-Hee, Ahn Mi Sun, Jung Yongsik, Roh Jin, Park So Hyun, Kim Tae-Gyu, Choi Jin-Hyuk, Kang Seok Y |
Genetic Analysis of Korean Adult Patients with Nontuberculous Mycobacteria Suspected of Primary Ciliary Dyskinesia Using Whole Exome Sequencing. Yonsei medical journal 2021 2 62 (3): 224-230. Cho Eun Hye, Ki Chang Seok, Yun Sun Ae, Kim Su Young, Jhun Byung Woo, Koh Won Jung, Huh Hee Jae, Lee Nam Yo |
Precise Identification of Recurrent Somatic Mutations in Oral Cancer Through Whole-Exome Sequencing Using Multiple Mutation Calling Pipelines. Frontiers in oncology 2021 12 11 741626. Lin Li-Han, Chou Chung-Hsien, Cheng Hui-Wen, Chang Kuo-Wei, Liu Chung- |
Novel Gene Variants Associated with Primary Ciliary Dyskinesia. Indian journal of pediatrics 2022 3 89 (7): 682-691. Demir Eksi Durkadin, Yilmaz Elanur, Basaran A Erdem, Erduran Gizem, Nur Banu, Mihci Ercan, Karadag Bulent, Bingol Aysen, Alper Ozgul |
Whole-Exome Sequencing Implicates the USP34 rs777591A > G Intron Variant in Chronic Obstructive Pulmonary Disease in a Kashi Cohort. Frontiers in cell and developmental biology 2021 9 792027. Xu Jingran, Li Li, Ren Jie, Zhong Xuemei, Xie Chengxin, Zheng Aifang, Abudukadier Ayiguzali, Tuerxun Maimaitiaili, Zhang Sujie, Tang Lifeng, Hairoula Dilare, Zou Xiaogua |
HYDIN mutation status as a potential predictor of immune checkpoint inhibitor efficacy in melanoma. Aging 2023 8 15 . Liu Li, Kuang Tianrui, Li Chunlei, Qiu Zhendong, Chen Xiaoyan, Deng Wenho |
Novel HYDIN variants associated with male infertility in two Chinese families. Frontiers in endocrinology 2023 2 14 1118841. Yu Hui, Shi Xiao, Shao Zhongmei, Geng Hao, Guo Senzhao, Li Kuokuo, Gu Meng, Xu Chuan, Gao Yang, Tan Qing, Duan Zongliu, Wu Huan, Hua Rong, Guo Rui, Wei Zhaolian, Zhou Ping, Cao Yunxia, He Xiaojin, Li Liang, Zhang Xiaoping, Lv Mingro |
Ciliary Ultrastructure Assessed by Transmission Electron Microscopy in Adults with Bronchiectasis and Suspected Primary Ciliary Dyskinesia but Inconclusive Genotype. Cells 2023 11 12 (22): . Ben O Staar, Jan Hegermann, Bernd Auber, Raphael Ewen, Sandra von Hardenberg, Ruth Olmer, Isabell Pink, Jessica Rademacher, Martin Wetzke, Felix C Ringshaus |
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