Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians
Xuehao Xiu, Haoyang Zhang, Angli Xue et al. · BMC Medicine · 2022
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Widespread and tissue-specific expression of endogenous retroelements in human somatic tissues
Jean-David Larouche, Assya Trofimov, Leslie Hesnard et al. · Genome Medicine · 2020
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ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP
Yvonne Nitschke, Yan Yan, Insa Buers et al. · Experimental and Molecular Medicine · 2018
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Racial and ethnic variation in multigene panel testing in a cohort of BRCA1/2‐negative individuals who had genetic testing in a large urban comprehensive cancer center
Sushma Tatineni, Meri Tarockoff, Nadine Abdallah et al. · Cancer Medicine · 2022
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Genetic and clinical characteristics of 24 mainland Chinese patients with CTNNB1 loss‐of‐function variants
Dan Yan, Yu Sun, Na Xu et al. · Molecular Genetics & Genomic Medicine · 2022
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Angiomotin mutation causes glomerulopathy and renal cysts by upregulating hepatocyte nuclear factor transcriptional activity
Yaochun Zhang, Liangjian Lu, Zhenhua Hu et al. · Clinical and Translational Medicine · 2022
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Corrigendum: Genetic Determinants of Visit-to-Visit Lipid Variability: Genome-Wide Association Study in Statin-Naïve Korean Population
Jun-Bean Park, Eunsoon Shin, Jong-Eun Lee et al. · Frontiers in Cardiovascular Medicine · 2022
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Human T Cells Expressing a CD19 CAR-T Receptor Provide Insights into Mechanisms of Human CD19-Positive β Cell Destruction
Haiting Ma, Jacob F. Jeppesen, Rudolf Jaenisch · Cell Reports Medicine · 2020
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In silico analysis of likely pathogenic variants in human GGCX gene
Mozan Osman Hassan, Doaa A. Gassim, Afraa M. Albakrye et al. · Informatics in Medicine Unlocked · 2020
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A fetus with meckel-gruber syndrome associated with isomerism
Kitova Tanya, Kilova Kristina, Kitov Borislav et al. · Open Medicine · 2014
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Genetics and genetic counseling in psychiatry: Results from an opinion survey of professionals and users
Lourdes Martorell, Annabel Sanfeliu, Ana Blázquez et al. · Molecular Genetics & Genomic Medicine · 2019
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8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects
Ikhlas Ben Ayed, Amal Bouzid, Fatma Kammoun et al. · Molecular Genetics & Genomic Medicine · 2021
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A case report of Klinefelter syndrome with Schizophrenia-like psychosis and seizure disorder
Anu Rita Jayaraman, Maithreyi Poguri, Nambi Siva · Indian Journal of Psychological Medicine · 2015
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Changes in FTO and IRX3 gene expression in obese and overweight male adolescents undergoing an intensive lifestyle intervention and the role of FTO genotype in this interaction
Saeid Doaei, Naser Kalantari, Pantea Izadi et al. · Journal of Translational Medicine · 2019
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Associations of pathogenic mutations responsible for breast cancer risk with histology and immunohistochemistry in Romanian population
Goidescu Iulian Gabriel, Eniu Dan Tudor, Caracostea Gabriela Valentina et al. · Romanian Journal of Laboratory Medicine · 2018
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Broad clinical manifestations of polygenic risk for coronary artery disease in the Women’s Health Initiative
Shoa L. Clarke, Matthew Parham, Joanna Lankester et al. · Communications Medicine · 2022
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Germline mutations in penetrant cancer predisposition genes are rare in men with prostate cancer selecting active surveillance
Lauren Brady, Lisa F. Newcomb, Kehao Zhu et al. · Cancer Medicine · 2022
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Investigating causal relations between sleep duration and risks of adverse pregnancy and perinatal outcomes: linear and nonlinear Mendelian randomization analyses
Qian Yang, Maria C. Magnus, Fanny Kilpi et al. · BMC Medicine · 2022
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Clinical RNA sequencing confirms compound heterozygous intronic variants in RYR1 in a patient with congenital myopathy, respiratory failure, neonatal brain hemorrhage, and d‐transposition of the great arteries
Amelle Shillington, Alonso Zea Vera, Tanya Perry et al. · Molecular Genetics & Genomic Medicine · 2021
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Treatment With Methotrexate Associated With Lipid Core Nanoparticles Prevents Aortic Dilation in a Murine Model of Marfan Syndrome
Maria Carolina Guido, Natalia de Menezes Lopes, Camila Inagaki Albuquerque et al. · Frontiers in Cardiovascular Medicine · 2022
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