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Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes
Andrews, Afiya, Maharaj, Avinaash, Cottrell, Emily, Chatterjee, Sumana, Shah, Pratik, Denvir, Louise, Dumic, Katja, Bossowski, Artur, Mushtaq, Talat, Vukovic, Rade, Didi, Mohamed, Shaw, Nick, Metherell, Louise A, Savage, Martin O, Storr, Helen L
Published in The journal of clinical endocrinology and metabolism (01.11.2021)
Published in The journal of clinical endocrinology and metabolism (01.11.2021)
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Genomic alterations are associated with response to aromatase inhibitor therapy for ER-positive postmenopausal ductal carcinoma in situ: (CALGB 40903, Alliance)
Marks, Jeffrey R., Zhang, Dadong, Hardman, Timothy, Chen, Yunn-yi, Hall, Allison, Simpson, Lunden, Hieken, Tina, Bedrosian, Isabelle, Price, Elissa, Sheng, Jeff, Dai, Yanwan, Lee, Marissa, Sibley, Alexander B., Owzar, Kouros, Hwang, E. Shelley
Published in Breast cancer research : BCR (20.02.2025)
Published in Breast cancer research : BCR (20.02.2025)
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Effects of particulate air pollution on BPDE-DNA adducts, telomere length, and mitochondrial DNA copy number in human exhaled breath condensate and BEAS-2B cells
Pedklang, Naruporn, Navasumrit, Panida, Chompoobut, Chalida, Promvijit, Jeerawan, Hunsonti, Potchanee, Ruchirawat, Mathuros
Published in International journal of hygiene and environmental health (01.01.2025)
Published in International journal of hygiene and environmental health (01.01.2025)
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Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals
Girard, Simon L., Bourassa, Cynthia V., Lemieux Perreault, Louis-Philippe, Legault, Marc-André, Barhdadi, Amina, Ambalavanan, Amirthagowri, Brendgen, Mara, Vitaro, Frank, Noreau, Anne, Dionne, Ginette, Tremblay, Richard E., Dion, Patrick A., Boivin, Michel, Dubé, Marie-Pierre, Rouleau, Guy A.
Published in PloS one (10.10.2016)
Published in PloS one (10.10.2016)
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Dissection of mendelian predisposition and complex genetic architecture of craniovertebral junction malformation
Liu, Zhenlei, Du, Huakang, Zhao, Hengqiang, Cai, Siyi, Zhao, Sen, Niu, Yuchen, Li, Xiaoxin, Liu, Bowen, Huang, Yingzhao, Shao, Jiashen, Liu, Lian, Tian, Ye, Wu, Zhihong, Wu, Hao, Hu, Yue, Zhang, Terry Jianguo, Jian, Fengzeng, Wu, Nan
Published in Human genetics (01.01.2023)
Published in Human genetics (01.01.2023)
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Mitochondrial DNA copy number is reduced in male combat veterans with PTSD
Bersani, Francesco Saverio, Morley, Claire, Lindqvist, Daniel, Epel, Elissa S., Picard, Martin, Yehuda, Rachel, Flory, Janine, Bierer, Linda M., Makotkine, Iouri, Abu-Amara, Duna, Coy, Michelle, Reus, Victor I., Lin, Jue, Blackburn, Elizabeth H., Marmar, Charles, Wolkowitz, Owen M., Mellon, Synthia H.
Published in Progress in neuro-psychopharmacology & biological psychiatry (04.01.2016)
Published in Progress in neuro-psychopharmacology & biological psychiatry (04.01.2016)
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Loss of chromosome Y leads to down regulation of KDM5D and KDM6C epigenetic modifiers in clear cell renal cell carcinoma
Arseneault, Madeleine, Monlong, Jean, Vasudev, Naveen S., Laskar, Ruhina S., Safisamghabadi, Maryam, Harnden, Patricia, Egevad, Lars, Nourbehesht, Nazanin, Panichnantakul, Pudchalaluck, Holcatova, Ivana, Brisuda, Antonin, Janout, Vladimir, Kollarova, Helena, Foretova, Lenka, Navratilova, Marie, Mates, Dana, Jinga, Viorel, Zaridze, David, Mukeria, Anush, Jandaghi, Pouria, Brennan, Paul, Brazma, Alvis, Tost, Jorg, Scelo, Ghislaine, Banks, Rosamonde E., Lathrop, Mark, Bourque, Guillaume, Riazalhosseini, Yasser
Published in Scientific reports (23.03.2017)
Published in Scientific reports (23.03.2017)
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Mitochondrial DNA and Epigenetics: Investigating Interactions with the One-Carbon Metabolism in Obesity
Bordoni, Laura, Petracci, Irene, Mlodzik-Czyzewska, Monika, Malinowska, Anna M., Szwengiel, Artur, Sadowski, Marcin, Gabbianelli, Rosita, Chmurzynska, Agata
Published in Oxidative medicine and cellular longevity (2022)
Published in Oxidative medicine and cellular longevity (2022)
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A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa
Wang, K, Zhang, H, Bloss, C S, Duvvuri, V, Kaye, W, Schork, N J, Berrettini, W, Hakonarson, H
Published in Molecular psychiatry (01.09.2011)
Published in Molecular psychiatry (01.09.2011)
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The KIR repertoire of a West African chimpanzee population is characterized by limited gene, allele, and haplotype variation
de Groot, Natasja G., Heijmans, Corrine M.C., van der Wiel, Marit K.H., Bruijnesteijn, Jesse, Bontrop, Ronald E.
Published in Frontiers in Immunology (11.12.2023)
Published in Frontiers in Immunology (11.12.2023)
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Cohort profile: SUPER-Finland – the Finnish study for hereditary mechanisms of psychotic disorders
Lähteenvuo, Markku, Ahola-Olli, Ari, Suokas, Kimmo, Holm, Minna, Misiewicz, Zuzanna, Jukuri, Tuomas, Männynsalo, Teemu, Wegelius, Asko, Haaki, Willehard, Kajanne, Risto, Kyttälä, Aija, Tuulio-Henriksson, Annamari, Lahdensuo, Kaisla, Häkkinen, Katja, Hietala, Jarmo, Paunio, Tiina, Niemi-Pynttäri, Jussi, Kieseppä, Tuula, Veijola, Juha, Lönnqvist, Jouko, Isometsä, Erkki, Kampman, Olli, Tiihonen, Jari, Hyman, Steven, Neale, Benjamin, Daly, Mark, Suvisaari, Jaana, Palotie, Aarno
Published in BMJ open (12.04.2023)
Published in BMJ open (12.04.2023)
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Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort
Bertelsen, Birgitte, Stefánsson, Hreinn, Riff Jensen, Lars, Melchior, Linea, Mol Debes, Nanette, Groth, Camilla, Skov, Liselotte, Werge, Thomas, Karagiannidis, Iordanis, Tarnok, Zsanett, Barta, Csaba, Nagy, Peter, Farkas, Luca, Brøndum-Nielsen, Karen, Rizzo, Renata, Gulisano, Mariangela, Rujescu, Dan, Kiemeney, Lambertus A., Tosato, Sarah, Nawaz, Muhammad Sulaman, Ingason, Andres, Unnsteinsdottir, Unnur, Steinberg, Stacy, Ludvigsson, Pétur, Stefansson, Kari, Kuss, Andreas Walter, Paschou, Peristera, Cath, Danielle, Hoekstra, Pieter J., Müller-Vahl, Kirsten, Stuhrmann, Manfred, Silahtaroglu, Asli, Pfundt, Rolph, Tümer, Zeynep
Published in Biological psychiatry (1969) (01.03.2016)
Published in Biological psychiatry (1969) (01.03.2016)
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Differential mitochondrial DNA copy number in three mood states of bipolar disorder
Wang, Dong, Li, Zongchang, Liu, Weiqing, Zhou, Jun, Ma, Xiaoqian, Tang, Jinsong, Chen, Xiaogang
Published in BMC psychiatry (25.05.2018)
Published in BMC psychiatry (25.05.2018)
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Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease
Stahel, Priska, Nahmias, Avital, Sud, Shawn K., Lee, So Jeong, Pucci, Andrea, Yousseif, Ahmed, Youseff, Alaa, Jackson, Timothy, Urbach, David R., Okrainec, Allan, Allard, Johane P., Sockalingam, Sanjeev, Yao, Tony, Barua, Moumita, Jiao, Hong, Magi, Reedik, Bassett, Anne S., Paterson, Andrew D., Dahlman, Ingrid, Batterham, Rachel L., Dash, Satya
Published in Diabetes (New York, N.Y.) (01.12.2019)
Published in Diabetes (New York, N.Y.) (01.12.2019)
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Mitochondrial DNA hypomethylation in chrome plating workers
Linqing, Yang, Bo, Xia, Xueqin, Yang, Hong, Ding, Desheng, Wu, Huimin, Zhang, Gaofeng, Jiang, Jianjun, Liu, Zhixiong, Zhuang
Published in Toxicology letters (22.01.2016)
Published in Toxicology letters (22.01.2016)
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Rare structural variation of synapse and neurotransmission genes in autism
Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S
Published in Molecular psychiatry (01.04.2012)
Published in Molecular psychiatry (01.04.2012)
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Normalized Testosterone Glucuronide as a Potential Urinary Biomarker for Highly Variable UGT2B17 in Children 7-18 Years
Zhang, Haeyoung, Basit, Abdul, Wolford, Chris, Chen, Kuan-Fu, Gaedigk, Andrea, Lin, Yvonne S, Leeder, J Steven, Prasad, Bhagwat
Published in Clinical pharmacology and therapeutics (01.05.2020)
Published in Clinical pharmacology and therapeutics (01.05.2020)
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Decreased Peripheral Mitochondrial DNA Copy Number is Associated with the Risk of Heart Failure and Long-term Outcomes
Huang, Jin, Tan, Lun, Shen, Rufei, Zhang, Lina, Zuo, Houjuan, Wang, Dao W.
Published in Medicine (Baltimore) (01.04.2016)
Published in Medicine (Baltimore) (01.04.2016)
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Copy Number Variations Analysis Identifies QPRT as a Candidate Gene Associated With Susceptibility for Solitary Functioning Kidney
Zhou, Xiao Y., Zheng, Hao Y., Han, Li, Wang, Yan, Zhang, Li, Shu, Xiao M., Zhang, Mu L., Liu, Guan N., Ding, Lian S.
Published in Frontiers in genetics (17.05.2021)
Published in Frontiers in genetics (17.05.2021)
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