Search Results - "Medical genetics

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  1. 1221
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    Genetic and toxinological divergence among populations of Tityus trivittatus Kraepelin, 1898 (Scorpiones: Buthidae) inhabiting Paraguay and Argentina. by Adolfo Borges, Antonieta Rojas de Arias, Sabrina de Almeida Lima, Bruno Lomonte, Cecilia Díaz, Carlos Chávez-Olórtegui, Matthew R Graham, Evanguedes Kalapothakis, Cathia Coronel, Adolfo R de Roodt

    Published 2020
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  2. 1222
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    Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population by Gong Yaoqin, Wang Aihua, Zhao Hailing, Fang QiuRong, Liu Qiji

    Published 2011
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  3. 1223
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    Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling by Yılmaz Kor, Minjing Zou, Roua A. Al-Rijjal, Dorota Monies, Brian F. Meyer, Yufei Shi

    Published 2018
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  4. 1224
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    Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis by Rivadeneira Fernando, Pols Huibert AP, Nevitt Michael C, Loughlin John, Lane Nancy E, Kloppenburg Margreet, Hofman Albert, Hart Deborah, Gonzalez Antonio, Carr Andrew, Meulenbelt Ingrid, Kerkhof Hanneke JM, Slagboom Eline P, Spector Tim D, Stolk Lisette, Tsezou Aspasia, Uitterlinden André G, Valdes Ana M, van Meurs Joyce BJ

    Published 2010
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  5. 1225
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    Evaluation of 22 genetic variants with Crohn's Disease risk in the Ashkenazi Jewish population: a case-control study by Ullman Thomas, Present Daniel H, Abreu Maria T, Doheny Dana, Hu Jianzhong, Erazo Monica, Ozelius Laurie, Mitchell Adele A, Peter Inga, Benkov Keith, Korelitz Burton I, Mayer Lloyd, Desnick Robert J

    Published 2011
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  6. 1226
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    Comprehensive analysis on phenotype and genetic basis of Chinese Fanconi anemia patients: dismal outcomes call for nationwide studies by Daijing Nie, Jing Zhang, Fang Wang, Wei Zhang, Lili Liu, Xue Chen, Yang Zhang, Panxiang Cao, Min Xiong, Tong Wang, Ping Wu, Xiaoli Ma, Wenjun Tian, Mangju Wang, Kylan N. Chen, Hongxing Liu

    Published 2020
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  7. 1227
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    Genetic and expression studies of <it>SMN2 </it>gene in Russian patients with spinal muscular atrophy type II and III by Schiöth Helgi B, Egorova Anna A, Chavan Rohit, Rask-Andersen Mathias, Vakharlovsky Viktor G, Kiselev Anton V, Zheleznyakova Galina, Baranov Vladislav S

    Published 2011
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  8. 1228
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    Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population by Ma Shi, Chen Ming, Rao Shaoqin, Liu Xiaoqi, Lu Fang, Wang Li, Yang Yang, Xian Yang, Li Ying, Zhang Xuejun, Tang Xin, Zhang Ben, Cai Li, Li Pengqiu, Lin Ying, Shi Yi, Bao Mingjing, Wu Jichuan, Yang Yan, Yang Jiyun, Yang Zhenglin

    Published 2010
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  9. 1229
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    Broadening our understanding of genetic risk for scleroderma/systemic sclerosis by querying the chromatin architecture surrounding the risk haplotypes by Kerry E. Poppenberg, Vincent M. Tutino, Evan Tarbell, James N. Jarvis

    Published 2021
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  10. 1230
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    Identification of genetic mechanisms underlying lipid metabolism-mediated tumor immunity in head and neck squamous cell carcinoma by Shaokun Liu, Shuning Wang, Zhenlin Wang

    Published 2023
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  11. 1231
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    Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes by Christopher S. Thom, Benjamin F. Voight

    Published 2020
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  12. 1232
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    Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis by Knüppel Sven, Esparza-Gordillo Jorge, Marenholz Ingo, Holzhütter Hermann-Georg, Bauerfeind Anja, Ruether Andreas, Weidinger Stephan, Lee Young-Ae, Rohde Klaus

    Published 2012
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  13. 1233
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    BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers by Shuo Zhang, Dingding Zhao, Jun Zhang, Yan Mao, Lingyin Kong, Yueping Zhang, Bo Liang, Xiaoxi Sun, Congjian Xu

    Published 2019
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  14. 1234
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    Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey by Mueller Patricia W, Ned Renée M, Yesupriya Ajay, Chang Man-huei, Dowling Nicole F

    Published 2010
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  15. 1235
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    How Pharmacogenomics Informs and Influences the Medication Experience by Anthony Olson, Jacob Brown

    Published 2024
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  16. 1236
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    Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India by Mehrotra Sanjana, Fakiola Michaela, Oommen Joyce, Jamieson Sarra E, Mishra Anshuman, Sudarshan Medhavi, Tiwary Puja, Rani Deepa, Thangaraj Kumarasamy, Rai Madhukar, Sundar Shyam, Blackwell Jenefer M

    Published 2011
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  17. 1237
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    Role of Autopsy and Genetic Testing in the Diagnosis of Perinatal Deaths due to Congenital Anomalies: A Cross-sectional Study by Asaranti Kar, Shreya Rath, Pallavi Bhuya, Sasmita Panda, Tushar Kar, Lity Mohanty, Lilabati Guru

    Published 2024
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  18. 1238
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    Genetic variation in interleukin-7 is associated with a reduced erythropoietic response in Kenyan children infected with Plasmodium falciparum by Lily E. Kisia, Prakasha Kempaiah, Samuel B. Anyona, Elly O. Munde, Angela O. Achieng, John M. Ong'echa, Christophe G. Lambert, Kiprotich Chelimo, Collins Ouma, Douglas J. Perkins, Evans Raballah

    Published 2019
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  19. 1239
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    Virtual CGH: an integrative approach to predict genetic abnormalities from gene expression microarray data applied in lymphoma by Iqbal Javeed, Geng Huimin, Chan Wing C, Ali Hesham H

    Published 2011
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  20. 1240
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    SIRT1 genetic variants associate with the metabolic response of Caucasians to a controlled lifestyle intervention - the TULIP Study by Stefan Norbert, Tschritter Otto, Machann Jürgen, Schick Fritz, Reinhardt Julia, Machicao Fausto, Weyrich Peter, Fritsche Andreas, Häring Hans-Ulrich

    Published 2008
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