Search Results - "Medical genetics

Genetic Referral Patterns and Responses to Clinical Scenarios: A Survey of Primary Care Providers and Clinical Geneticists by Tina K. Truong, Aileen Kenneson, Ami R. Rosen, Rani H. Singh

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Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study by Zhang Ying, MacCluer Jean W, North Kari E, DeCroo Susan, Ferrell Robert E, Best Lyle G, Lee Elisa T, Howard Barbara V, Umans Jason, Palmieri Vittorio, Garred Peter

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Genetic interaction effects reveal lipid-metabolic and inflammatory pathways underlying common metabolic disease risks by Hyung Jun Woo, Jaques Reifman

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Genetic Polymorphisms in NLRP3 Inflammasome-Associated Genes in Patients with B-Cell Non-Hodgkin’s Lymphoma by Liu ZH, Zhang L, Jing FJ, Xiao SX, Gao Y, Bian HY, Zhao X

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Genetic variations in <it>APPL2 </it>are associated with overweight and obesity in a Chinese population with normal glucose tolerance by Jiang Shan, Fang Qichen, Yu Weihui, Zhang Rong, Hu Cheng, Dong Kun, Bao Yuqian, Wang Chen, Xiang Kunsan, Jia Weiping

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Model of genetic and environmental factors associated with type 2 diabetes mellitus in a Chinese Han population by Zheng Li, Cheng-yin Ye, Tian-Yu Zhao, Lei Yang

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Deleterious genetic variants in ciliopathy genes increase risk of ritodrine-induced cardiac and pulmonary side effects by Heewon Seo, Eun Jin Kwon, Young-Ah You, Yoomi Park, Byung Joo Min, Kyunghun Yoo, Han-Sung Hwang, Ju Han Kim, Young Ju Kim

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Desire for genetically related children among transgender and gender-diverse patients seeking gender-affirming hormones by Moira A. Kyweluk, Ph.D., M.P.H, Jerrica Kirkley, M.D, Frances Grimstad, M.D., M.S, Paula Amato, M.D, Jae Downing, Ph.D

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Functional and genetic analysis in type 2 diabetes of Liver X receptor alleles - a cohort study by Gustafsson Jan-Åke, Brismar Kerstin, Östenson Claes G, Efendic Suad, Lecoeur Cecile, Gu Harvest F, Nilsson Maria, Dahlman Ingrid, Froguel Philippe, Vaxillaire Martine, Dahlman-Wright Karin, Steffensen Knut R

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Genetic polymorphisms of innate immunity-related inflammatory pathways and their association with factors related to type 2 diabetes by Spector Timothy D, Malik Suneil, Villegas Andre, Brenner Darren, Dastani Zari, Garcia-Bailo Bibiana, Arora Paul, Richards Brent, El-Sohemy Ahmed, Karmali Mohamed, Badawi Alaa

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Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients by Mikael Koponen, Aki S. Havulinna, Annukka Marjamaa, Annukka M. Tuiskula, Veikko Salomaa, Päivi J. Laitinen-Forsblom, Kirsi Piippo, Lauri Toivonen, Kimmo Kontula, Matti Viitasalo, Heikki Swan

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Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors by Nadeau G, Ouimet-Grennan E, Aaron M, Drouin S, Bertout L, Shalmiev A, Beaulieu P, St-Onge P, Veilleux LN, Rauch F, Petrykey K, Laverdière C, Sinnett D, Alos N, Krajinovic M

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TPMT Genetic Variability and Its Association with Hematotoxicity in Indonesian Children with Acute Lymphoblastic Leukemia in Maintenance Therapy by Rosdiana DS, Setiabudy R, Andalusia R, Gatot D, Louisa M, Bardosono S, Instiaty I

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Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review by Prince AER, Cadigan RJ, Henderson GE, Evans JP, Adams M, Coker-Schwimmer E, Penn DC, Van Riper M, Corbie-Smith G, Jonas DE

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Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization study by Miao Chen, Zhen Wang, Hongfei Xu, Xiaofang Chen, Peng Teng, Liang Ma

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Preclinical Animal Modeling in Medicine

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Improving Trend of Adhering to Ethical Measures in Iranian Research in Human Genetics: A Survey from 2005 to 2009; and the Road Ahead. by Seyed Hasan Saadat, Khodabakhsh Ahmadi, Fakhruddin Feyzi, Mostafa Ghanei

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An alpha-helix variant p.Arg156Pro in LMNA as a cause of hereditary dilated cardiomyopathy: genetics and bioinfomatics exploration by Lei Chang, Rong Huang, Jianzhou Chen, Guannan Li, Guangfei Shi, Biao Xu, Lian Wang

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Effects of Comedication and Genetic Factors on the Population Pharmacokinetics of Lamotrigine: A Prospective Analysis in Chinese Patients With Epilepsy by Zhan-zhang Wang, Zhan-zhang Wang, Yue-feng Zhang, Wen-can Huang, Wen-can Huang, Xi-pei Wang, Xiao-jiao Ni, Hao-yang Lu, Jin-qing Hu, Shu-hua Deng, Xiu-qing Zhu, Huan-shan Xie, Hong-zhen Chen, Ming Zhang, Chang Qiu, Yu-guan Wen, Yu-guan Wen, De-wei Shang, De-wei Shang

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Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population by Sumbal Sarwar, Shabana, Amna Tahir, Zainab Liaqat, Saher Naseer, Rani Summeya Seme, Sabahat Mehmood, Saleem Ullah Shahid, Shahida Hasnain

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