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Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12
Kanwal, Sumaira, Kongju National University, Gongju, Republic of Korea, Choi, B.O., Ewha Womans University, School of Medicine, Seoul, Republic of Korea, Kim, S.B., Kyung Hee University, School of Medicine, Seoul, Republic of Korea, Koo, H.S., Ewha Womans University, School of Medicine, Seoul, Republic of Korea, Kim, J.Y., Ewha Womans University, School of Medicine, Seoul, Republic of Korea, Hyun, Y.S., Kongju National University, Gongju, Republic of Korea, Lee, H.J., Kongju National University, Gongju, Republic of Korea, Chung, K.W., Kongju National University, Gongju, Republic of Korea
Published in Animal cells and systems (01.12.2011)
Published in Animal cells and systems (01.12.2011)
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Molecular Phenotyping of Human Endometrium Distinguishes Menstrual Cycle Phases and Underlying Biological Processes in Normo-Ovulatory Women
Talbi, S., Hamilton, A. E., Vo, K. C., Tulac, S., Overgaard, M. T., Dosiou, C., Le Shay, N., Nezhat, C. N., Kempson, R., Lessey, B. A., Nayak, N. R., Giudice, L. C.
Published in Endocrinology (Philadelphia) (01.03.2006)
Published in Endocrinology (Philadelphia) (01.03.2006)
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Polygenic Scores of Alzheimer's Disease Risk Genes Add Only Modestly to APOE in Explaining Variation in Amyloid PET Burden
Ramanan, Vijay K, Heckman, Michael G, Przybelski, Scott A, Lesnick, Timothy G, Lowe, Val J, Graff-Radford, Jonathan, Mielke, M, Jack, Clifford R, Knopman, David S, Petersen, Ronald C, Ross, Owen A, Vemuri, Prashanthi
Published in Journal of Alzheimer's disease (01.01.2022)
Published in Journal of Alzheimer's disease (01.01.2022)
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Association between OX40L polymorphism and type 2 diabetes mellitus in Iranians
Jahromi, Abdolreza Sotoodeh, Erfanian, Saiedeh, Roustazadeh, Abazar
Published in BMC medical genomics (09.07.2024)
Published in BMC medical genomics (09.07.2024)
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The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults
Cao, Hengyi, Harneit, Anais, Walter, Henrik, Erk, Susanne, Braun, Urs, Moessnang, Carolin, Geiger, Lena S, Zang, Zhenxiang, Mohnke, Sebastian, Heinz, Andreas, Romanczuk-Seiferth, Nina, Mühleisen, Thomas, Mattheisen, Manuel, Witt, Stephanie H, Cichon, Sven, Nöthen, Markus M, Rietschel, Marcella, Meyer-Lindenberg, Andreas, Tost, Heike
Published in Neuropsychopharmacology (New York, N.Y.) (01.01.2018)
Published in Neuropsychopharmacology (New York, N.Y.) (01.01.2018)
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Brain Expressed microRNAs Implicated in Schizophrenia Etiology
Hansen, Thomas, Olsen, Line, Lindow, Morten, Jakobsen, Klaus D., Ullum, Henrik, Jonsson, Erik, Andreassen, Ole A., Djurovic, Srdjan, Melle, Ingrid, Agartz, Ingrid, Hall, Håkan, Timm, Sally, Wang, August G., Werge, Thomas
Published in PloS one (12.09.2007)
Published in PloS one (12.09.2007)
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Genomic Profiles of Diversification and Genotype–Phenotype Association in Island Nematode Lineages
McGaughran, Angela, Rödelsperger, Christian, Grimm, Dominik G., Meyer, Jan M., Moreno, Eduardo, Morgan, Katy, Leaver, Mark, Serobyan, Vahan, Rakitsch, Barbara, Borgwardt, Karsten M., Sommer, Ralf J.
Published in Molecular biology and evolution (01.09.2016)
Published in Molecular biology and evolution (01.09.2016)
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Effects of early introduction of non‐invasive positive pressure ventilation based on forced vital capacity rate of change: Variation across amyotrophic lateral sclerosis clinical phenotypes
Elamin, Elamin M., Wilson, Catherine S., Sriaroon, Chakrapol, Crudup, Bianca, Pothen, Sophia, Kang, Younghee C., White, Kevin T., Anderson, William M.
Published in International journal of clinical practice (Esher) (01.01.2019)
Published in International journal of clinical practice (Esher) (01.01.2019)
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Clinical Phenotype and Mutation Spectrum of Alzheimer's Disease with Causative Genetic Mutation in a Chinese Cohort
Mao, Chenhui, Li, Jie, Dong, Liling, Huang, Xinying, Lei, Dan, Wang, Jie, Chu, Shanshan, Liu, Caiyan, Peng, Bin, Román, Gustavo C, Cui, Liying, Gao, Jing
Published in Current Alzheimer research (01.01.2021)
Published in Current Alzheimer research (01.01.2021)
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Identification of bovine CpG SNPs as potential targets for epigenetic regulation via DNA methylation
Maldonado, Mariângela B. C., de Rezende Neto, Nelson B., Nagamatsu, Sheila T., Carazzolle, Marcelo F., Hoff, Jesse L., Whitacre, Lynsey K., Schnabel, Robert D., Behura, Susanta K., McKay, Stephanie D., Taylor, Jeremy F., Lopes, Flavia L.
Published in PloS one (12.09.2019)
Published in PloS one (12.09.2019)
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Association of cholesterol and glycemic state biomarkers with phenotypic variation and Parkinson's disease progression: The Oxford Discovery cohort
Ho Chiu, Nicholas Kwan, Lawton, Michael, Zerenner, Tanja, Morovat, Alireza, Welch, Jessica, Razzaque, Jamil, Hu, Michele T, Ben-Shlomo, Yoav
Published in Journal of Parkinson's disease (01.05.2025)
Published in Journal of Parkinson's disease (01.05.2025)
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Quiescence unveils a novel mutational force in fission yeast
Gangloff, Serge, Achaz, Guillaume, Francesconi, Stefania, Villain, Adrien, Miled, Samia, Denis, Claire, Arcangioli, Benoit
Published in eLife (18.12.2017)
Published in eLife (18.12.2017)
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