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Potential Cross Talk between Autism Risk Genes and Neurovascular Molecules: A Pilot Study on Impact of Blood Brain Barrier Integrity
Jagadapillai, Rekha, Qiu, Xiaolu, Ojha, Kshama, Li, Zhu, El-Baz, Ayman, Zou, Shipu, Gozal, Evelyne, Barnes, Gregory N.
Published in Cells (Basel, Switzerland) (15.07.2022)
Published in Cells (Basel, Switzerland) (15.07.2022)
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Copy number variations of obesity relevant loci associated with body mass index in young Chinese
Sun, Chen, Cao, Min, Shi, Juan, Li, Lijuan, Miao, Lin, Hong, Jie, Cui, Bin, Ning, Guang
Published in Gene (10.03.2013)
Published in Gene (10.03.2013)
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Population Specific Impact of Genetic Variants in KCNJ11 Gene to Type 2 Diabetes: A Case-Control and Meta-Analysis Study
Phani, Nagaraja M., Guddattu, Vasudeva, Bellampalli, Ravishankara, Seenappa, Venu, Adhikari, Prabha, Nagri, Shivashankara K., D′Souza, Sydney C., Mundyat, Gopinath P., Satyamoorthy, Kapaettu, Rai, Padmalatha S.
Published in PloS one (23.09.2014)
Published in PloS one (23.09.2014)
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A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15
Casamassa, Alessia, Ferrari, Daniela, Gelati, Maurizio, Carella, Massimo, Vescovi, Angelo Luigi, Rosati, Jessica
Published in International journal of molecular sciences (09.03.2020)
Published in International journal of molecular sciences (09.03.2020)
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A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model
Rudd, Danielle S., Axelsen, Michael, Epping, Eric A., Andreasen, Nancy C., Wassink, Thomas H.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2014)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2014)
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A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer
Liu, Bin, Yang, Lei, Huang, Binfang, Cheng, Mei, Wang, Hui, Li, Yinyan, Huang, Dongsheng, Zheng, Jian, Li, Qingchu, Zhang, Xin, Ji, Weidong, Zhou, Yifeng, Lu, Jiachun
Published in American journal of human genetics (10.08.2012)
Published in American journal of human genetics (10.08.2012)
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Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous Thromboembolism
Sticchi, Elena, Magi, Alberto, Kamstrup, Pia R., Marcucci, Rossella, Prisco, Domenico, Martinelli, Ida, Mannucci, Pier Mannuccio, Abbate, Rosanna, Giusti, Betti
Published in PloS one (22.02.2016)
Published in PloS one (22.02.2016)
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Autism and chromosome abnormalities-A review
Bergbaum, Anne, Ogilvie, Caroline Mackie
Published in Clinical anatomy (New York, N.Y.) (01.07.2016)
Published in Clinical anatomy (New York, N.Y.) (01.07.2016)
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The Impact of Copy Number Deletions on General Cognitive Ability and Ventricle Size in Patients with Schizophrenia and Healthy Control Subjects
Yeo, Ronald A., Gangestad, Steven W., Liu, Jingyu, Ehrlich, Stefan, Thoma, Robert J., Pommy, Jessica, Mayer, Andrew R., Schulz, S. Charles, Wassink, Thomas H., Morrow, Eric M., Bustillo, Juan R., Sponheim, Scott R., Ho, Beng-Choon, Calhoun, Vince D.
Published in Biological psychiatry (1969) (15.03.2013)
Published in Biological psychiatry (1969) (15.03.2013)
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Copy number variations in East-Asian population and their evolutionary and functional implications
Yim, Seon-Hee, Kim, Tae-Min, Hu, Hae-Jin, Kim, Ji-Hong, Kim, Bong-Jo, Lee, Jong-Young, Han, Bok-Ghee, Shin, Seung-Hun, Jung, Seung-Hyun, Chung, Yeun-Jun
Published in Human molecular genetics (15.03.2010)
Published in Human molecular genetics (15.03.2010)
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Integrative genomic and network analysis identified novel genes associated with the development of advanced cervical squamous cell carcinoma
Roychowdhury, Anirban, Samadder, Sudip, Das, Pijush, Mandloi, Sapan, Addya, Sankar, Chakraborty, Chandraditya, Basu, Partha Sarathi, Mondal, Ranajit, Roy, Anup, Chakrabarti, Saikat, Roychoudhury, Susanta, Panda, Chinmay Kumar
Published in Biochimica et biophysica acta. General subjects (01.01.2017)
Published in Biochimica et biophysica acta. General subjects (01.01.2017)
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A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens
Chen, Songchang, Liu, Deyuan, Zhang, Junyu, Li, Shuyuan, Zhang, Lanlan, Fan, Jianxia, Luo, Yuqin, Qian, Yeqing, Huang, Hefeng, Liu, Chao, Zhu, Huanhuan, Jiang, Zhengwen, Xu, Chenming
Published in Prenatal diagnosis (01.02.2017)
Published in Prenatal diagnosis (01.02.2017)
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Increased CNV-Region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample
Guffanti, Guia, Torri, Federica, Rasmussen, Jerod, Clark, Andrew P., Lakatos, Anita, Turner, Jessica A., Fallon, James H., Saykin, Andrew J., Weiner, Michael, Vawter, Marquis P., Knowles, James A., Potkin, Steven G., Macciardi, Fabio
Published in Genomics (San Diego, Calif.) (01.08.2013)
Published in Genomics (San Diego, Calif.) (01.08.2013)
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Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
Pagnamenta, Alistair T, Khan, Hameed, Walker, Susan, Gerrelli, Dianne, Wing, Kirsty, Bonaglia, Maria Clara, Giorda, Roberto, Berney, Tom, Mani, Elisa, Molteni, Massimo, Pinto, Dalila, Le Couteur, Ann, Hallmayer, Joachim, Sutcliffe, James S, Szatmari, Peter, Paterson, Andrew D, Scherer, Stephen W, Vieland, Veronica J, Monaco, Anthony P
Published in Journal of medical genetics (01.01.2011)
Published in Journal of medical genetics (01.01.2011)
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Nance–Horan syndrome pedigree due to a novel microdeletion and skewed X chromosome inactivation
Huang, Yazhou, Ma, Linya, Zhang, Zhaoxia, Nie, Shujuan, Zhou, Yuan, Zhang, Jibo, Wang, Chao, Fang, Xingxin, Quan, Yingting, He, Ting, Liu, Anhui, Peng, Dan
Published in Molecular genetics & genomic medicine (01.02.2023)
Published in Molecular genetics & genomic medicine (01.02.2023)
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