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A genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies
Murry, Jaclyn B., Santos, Xiomara M., Wang, Xiaoling, Wan, Ying-Wooi, Van den Veyver, Ignatia B., Dietrich, Jennifer E.
Published in Fertility and sterility (01.02.2015)
Published in Fertility and sterility (01.02.2015)
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Abundant copy-number loss of CYCLOPS and STOP genes in gastric adenocarcinoma
Cutcutache, Ioana, Wu, Alice Yingting, Suzuki, Yuka, McPherson, John Richard, Lei, Zhengdeng, Deng, Niantao, Zhang, Shenli, Wong, Wai Keong, Soo, Khee Chee, Chan, Weng Hoong, Ooi, London Lucien, Welsch, Roy, Tan, Patrick, Rozen, Steven G.
Published in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association (01.04.2016)
Published in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association (01.04.2016)
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Unique genetic profile of sporadic colorectal cancer liver metastasis versus primary tumors as defined by high-density single-nucleotide polymorphism arrays
Muñoz-Bellvis, Luís, Fontanillo, Celia, González-González, María, Garcia, Eva, Iglesias, Manuel, Esteban, Carmen, Gutierrez, M L, Abad, M M, Bengoechea, Oscar, De Las Rivas, Javier, Orfao, Alberto, Sayagués, J M
Published in Modern pathology (01.04.2012)
Published in Modern pathology (01.04.2012)
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Mytype: A Capture Based Sequencing Approach to Detect Somatic Mutations, Copy Number Changes and IGH Translocations in Multiple Myeloma
Yellapantula, Venkata, Hultcrantz, Malin, Rustad, Even H, Landau, Heather J., Iacobuzio-Donahue, Christine, Akhlaghi, Theresia, Amit, Ido, Ledergor, Guy, Korde, Neha, Mailankody, Sham, Kazandjian, Dickran, Patel, Akshar, Bolli, Niccolo, Papaemmanuil, Elli, Landgren, Ola
Published in Blood (29.11.2018)
Published in Blood (29.11.2018)
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The Alu-Rich Genomic Architecture of SPAST Predisposes to Diverse and Functionally Distinct Disease-Associated CNV Alleles
Boone, Philip M., Yuan, Bo, Campbell, Ian M., Scull, Jennifer C., Withers, Marjorie A., Baggett, Brett C., Beck, Christine R., Shaw, Christine J., Stankiewicz, Pawel, Moretti, Paolo, Goodwin, Wendy E., Hein, Nichole, Fink, John K., Seong, Moon-Woo, Seo, Soo Hyun, Park, Sung Sup, Karbassi, Izabela D., Batish, Sat Dev, Ordóñez-Ugalde, Andrés, Quintáns, Beatriz, Sobrido, María-Jesús, Stemmler, Susanne, Lupski, James R.
Published in American journal of human genetics (07.08.2014)
Published in American journal of human genetics (07.08.2014)
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Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons
Zhang, Siming, Zhang, Xianglong, Purmann, Carolin, Ma, Shining, Shrestha, Anima, Davis, Kasey N., Ho, Marcus, Huang, Yiling, Pattni, Reenal, Wong, Wing Hung, Bernstein, Jonathan A., Hallmayer, Joachim, Urban, Alexander E.
Published in Biological psychiatry (1969) (01.03.2021)
Published in Biological psychiatry (1969) (01.03.2021)
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Detection of local DNA copy number changes in lung cancer population analyses using a multi-scale approach
Kachouie, Nezamoddin N., Lin, Xihong, Christiani, David C., Schwartzman, Armin
Published in Communication in statistics. Case studies and data analysis (02.10.2015)
Published in Communication in statistics. Case studies and data analysis (02.10.2015)
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TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia
Ogata, Tsutomu, Niihori, Tetsuya, Tanaka, Noriko, Kawai, Masahiko, Nagashima, Takeshi, Funayama, Ryo, Nakayama, Keiko, Nakashima, Shinichi, Kato, Fumiko, Fukami, Maki, Aoki, Yoko, Matsubara, Yoichi
Published in PloS one (17.03.2014)
Published in PloS one (17.03.2014)
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TNFRSF14 and EZH2 Mutations, Chr2p Gain and Copy Number Changes Targeting Genes Whose Proteins Interact with the Microenvironment In Transformed Follicular Lymphoma
Wrench, David, Sangaralingam, Ajanthah, Tayyib, Hira, Kang, Myung-Kuk, O'Riain, Ciaran, Gupta, Manu, Carlotti, Emanuela, Bodor, Csaba, Iqbal, Sameena, Chaplin, Tracy, Matthews, Janet, Clear, Andrew James, Davies, Andrew, Montoto, Silvia, Calaminici, Maria, Young, Bryan D, Gribben, John G., Lister, Andrew, Fitzgibbon, Jude
Published in Blood (19.11.2010)
Published in Blood (19.11.2010)
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Contribution of Spontaneous Mutations to Quantitative and Molecular Variation at the Highly Repetitive rDNA Locus in Yeast
Sharp, Nathaniel P, Smith, Denise R, Driscoll, Gregory, Sun, Kexin, Vickerman, Catherine M, Martin, Sterling C T
Published in Genome biology and evolution (06.10.2023)
Published in Genome biology and evolution (06.10.2023)
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Association of copy number variation in the AHI1 gene with risk of obesity in the Chinese population
Huang, Liansha, Teng, Dacai, Wang, Hao, Sheng, Guoqing, Liu, Tonghua
Published in European journal of endocrinology (01.04.2012)
Published in European journal of endocrinology (01.04.2012)
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