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The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions
Bolouri, Hamid, Farrar, Jason E, Triche, Jr, Timothy, Ries, Rhonda E, Lim, Emilia L, Alonzo, Todd A, Ma, Yussanne, Moore, Richard, Mungall, Andrew J, Marra, Marco A, Zhang, Jinghui, Ma, Xiaotu, Liu, Yu, Liu, Yanling, Guidry Auvil, Jaime M, Davidsen, Tanja M, Gesuwan, Patee, Hermida, Leandro C, Salhia, Bodour, Capone, Stephen, Ramsingh, Giridharan, Zwaan, Christian Michel, Noort, Sanne, Piccolo, Stephen R, Kolb, E Anders, Gamis, Alan S, Smith, Malcolm A, Gerhard, Daniela S, Meshinchi, Soheil
Published in Nature medicine (01.01.2018)
Published in Nature medicine (01.01.2018)
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Enhanced yield of chromosome aberrations after CT examinations in paediatric patients
Stephan, G., Schneider, K., Panzer, W., Walsh, L., Oestreicher, U.
Published in International journal of radiation biology (01.01.2007)
Published in International journal of radiation biology (01.01.2007)
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SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
Schilit, Samantha L.P., Menon, Shreya, Friedrich, Corinna, Kammin, Tammy, Wilch, Ellen, Hanscom, Carrie, Jiang, Sizun, Kliesch, Sabine, Talkowski, Michael E., Tüttelmann, Frank, MacQueen, Amy J., Morton, Cynthia C.
Published in American journal of human genetics (02.01.2020)
Published in American journal of human genetics (02.01.2020)
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18 F-FDG PET/CT scanning: Biological effects on patients: Entrance surface dose, DNA damage, and chromosome aberrations in lymphocytes
Prasad, Akshaya, Visweswaran, Shangamithra, Kanagaraj, Karthik, Raavi, Venkateswarlu, Arunan, M, Venkatachalapathy, E, Paneerselvam, S, Jose, M T, Ozhimuthu, Annalakshmi, Perumal, Venkatachalam
Published in Mutation research. Genetic toxicology and environmental mutagenesis (01.02.2019)
Published in Mutation research. Genetic toxicology and environmental mutagenesis (01.02.2019)
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome
Joshi, Ricky S., Garg, Paras, Zaitlen, Noah, Lappalainen, Tuuli, Watson, Corey T., Azam, Nidha, Ho, Daniel, Li, Xin, Antonarakis, Stylianos E., Brunner, Han G., Buiting, Karin, Cheung, Sau Wai, Coffee, Bradford, Eggermann, Thomas, Francis, David, Geraedts, Joep P., Gimelli, Giorgio, Jacobson, Samuel G., Le Caignec, Cedric, de Leeuw, Nicole, Liehr, Thomas, Mackay, Deborah J., Montgomery, Stephen B., Pagnamenta, Alistair T., Papenhausen, Peter, Robinson, David O., Ruivenkamp, Claudia, Schwartz, Charles, Steiner, Bernhard, Stevenson, David A., Surti, Urvashi, Wassink, Thomas, Sharp, Andrew J.
Published in American journal of human genetics (01.09.2016)
Published in American journal of human genetics (01.09.2016)
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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Brand, Harrison, Kammin, Tammy, Mitchell, Elyse, Hodge, Jennelle C, Hanscom, Carrie, Pillalamarri, Vamsee, Alkuraya, Fowzan S, Anderson, Mary-Anne, Antolik, Caroline, Anyane-Yeboa, Kwame, Bernstein, Jonathan A, Blumenthal, Ian, Bongers, Ernie M H F, Brown, Chester W, Brüggenwirth, Hennie T, Callewaert, Bert, Cox, Helen, Cuppen, Edwin, Currall, Benjamin B, Cushing, Tom, David, Dezso, Deardorff, Matthew A, Dheedene, Annelies, D'Hooghe, Marc, Earl, Dawn L, Ferguson, Heather L, FitzPatrick, David R, Gerrol, Pamela, Giachino, Daniela, Gliem, Troy, Griffis, Cristin, Gripp, Karen W, Gropman, Andrea L, Hanson-Kahn, Andrea, Harris, David J, Hill, Rosamund, Hoffman, Jodi D, Hopkin, Robert J, Hubshman, Monika W, Irons, Mira, Irving, Melita, Jacobsen, Jessie C, Janssens, Sandra, Jewett, Tamison, Johnson, John P, Koolen, David A, Lawless, William, Lemyre, Emmanuelle, Leppig, Kathleen, Levin, Alex V, Li, Hong, Liao, Eric C, Lose, Edward J, Lucente, Diane, Manavalan, Poornima, Mandrile, Giorgia, Marcelis, Carlo L, Masser-Frye, Diane, McClellan, Michael W, Menten, Björn, Middelkamp, Sjors, Moe, Emily, Mohammed, Shehla, Mononen, Tarja, Mortenson, Megan E, Moya, Graciela, Ordulu, Zehra, Parkash, Sandhya, Pauker, Susan P, Pereira, Shahrin, Perrin, Danielle, Phelan, Katy, Aguilar, Raul E Piña, Poddighe, Pino J, Pregno, Giulia, Raskin, Salmo, Reis, Linda, Rhead, William, Rita, Debra, Renkens, Ivo, Ruliera, Jayla, Schilit, Samantha L P, Shaheen, Ranad, Sparkes, Rebecca, Spiegel, Erica, Stevens, Blair, Tagoe, Julia, Thakuria, Joseph V, van de Kamp, Jiddeke, van Essen, Ton, van Ravenswaaij-Arts, Conny M, van Roosmalen, Markus J, Vergult, Sarah, Volker-Touw, Catharina M L, Wilson, Anna, Yerena-de Vega, Maria de la Concepcion A, Zori, Roberto T, Kloosterman, Wigard P, Morton, Cynthia C, Talkowski, Michael E
Published in Nature genetics (01.01.2017)
Published in Nature genetics (01.01.2017)
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Unrepaired clustered DNA lesions induce chromosome breakage in human cells
Asaithamby, Aroumougame, Hu, Burong, Chen, David J
Published in Proceedings of the National Academy of Sciences - PNAS (17.05.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (17.05.2011)
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Chromosomal aberration frequency in lymphocytes predicts the risk of cancer: results from a pooled cohort study of 22 358 subjects in 11 countries
Bonassi, Stefano, Norppa, Hannu, Ceppi, Marcello, Strömberg, Ulf, Vermeulen, Roel, Znaor, Ariana, Cebulska-Wasilewska, Antonina, Fabianova, Eleonora, Fucic, Alexandra, Gundy, Sarolta, Hansteen, Inger-Lise, Knudsen, Lisbeth E., Lazutka, Juozas, Rossner, Pavel, Sram, Radim J., Boffetta, Paolo
Published in Carcinogenesis (New York) (01.06.2008)
Published in Carcinogenesis (New York) (01.06.2008)
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Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing
Leary, Rebecca J, Sausen, Mark, Kinde, Isaac, Papadopoulos, Nickolas, Carpten, John D, Craig, David, O'Shaughnessy, Joyce, Kinzler, Kenneth W, Parmigiani, Giovanni, Vogelstein, Bert, Diaz, Jr, Luis A, Velculescu, Victor E
Published in Science translational medicine (28.11.2012)
Published in Science translational medicine (28.11.2012)
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The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay
Kirov, George, Rees, Elliott, Walters, James T.R., Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander L., Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J.
Published in Biological psychiatry (1969) (01.03.2014)
Published in Biological psychiatry (1969) (01.03.2014)
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Chromosome aberrations in peripheral blood lymphocytes of individuals living in high background radiation areas of Ramsar, Iran
Zakeri, F., Rajabpour, M. R., Haeri, S. A., Kanda, R., Hayata, I., Nakamura, S., Sugahara, T., Ahmadpour, M. J.
Published in Radiation and environmental biophysics (01.11.2011)
Published in Radiation and environmental biophysics (01.11.2011)
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Research progress on the etiology and pathogenesis of adolescent idiopathic scoliosis
Peng, Yue, Wang, Sheng-Ru, Qiu, Gui-Xing, Zhang, Jian-Guo, Zhuang, Qian-Yu
Published in Chinese medical journal (20.02.2020)
Published in Chinese medical journal (20.02.2020)
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Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer
Forsberg, Lars A, Rasi, Chiara, Malmqvist, Niklas, Davies, Hanna, Pasupulati, Saichand, Pakalapati, Geeta, Sandgren, Johanna, de Ståhl, Teresita Diaz, Zaghlool, Ammar, Giedraitis, Vilmantas, Lannfelt, Lars, Score, Joannah, Cross, Nicholas C P, Absher, Devin, Janson, Eva Tiensuu, Lindgren, Cecilia M, Morris, Andrew P, Ingelsson, Erik, Lind, Lars, Dumanski, Jan P
Published in Nature genetics (01.06.2014)
Published in Nature genetics (01.06.2014)
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Prognostic and predictive impact of genetic markers in patients with CLL treated with obinutuzumab and venetoclax
Tausch, Eugen, Schneider, Christof, Robrecht, Sandra, Zhang, Can, Dolnik, Anna, Bloehdorn, Johannes, Bahlo, Jasmin, Al-Sawaf, Othman, Ritgen, Matthias, Fink, Anna-Maria, Eichhorst, Barbara, Kreuzer, Karl-Anton, Tandon, Maneesh, Humphrey, Kathryn, Jiang, Yanwen, Schary, William, Bullinger, Lars, Mertens, Daniel, Lurà, Michele Porro, Kneba, Michael, Döhner, Hartmut, Fischer, Kirsten, Hallek, Michael, Stilgenbauer, Stephan
Published in Blood (25.06.2020)
Published in Blood (25.06.2020)
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Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants
Lefkowitz, Roy B., Tynan, John A., Liu, Tong, Wu, Yijin, Mazloom, Amin R., Almasri, Eyad, Hogg, Grant, Angkachatchai, Vach, Zhao, Chen, Grosu, Daniel S., McLennan, Graham, Ehrich, Mathias
Published in American journal of obstetrics and gynecology (01.08.2016)
Published in American journal of obstetrics and gynecology (01.08.2016)
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
Liu, Ke, Kurien, Biji T., Zimmerman, Sarah L., Kaufman, Kenneth M., Taft, Diana H., Kottyan, Leah C., Lazaro, Sara, Weaver, Carrie A., Ice, John A., Adler, Adam J., Chodosh, James, Radfar, Lida, Rasmussen, Astrid, Stone, Donald U., Lewis, David M., Li, Shibo, Koelsch, Kristi A., Igoe, Ann, Talsania, Mitali, Kumar, Jay, Maier‐Moore, Jacen S., Harris, Valerie M., Gopalakrishnan, Rajaram, Jonsson, Roland, Lessard, James A., Lu, Xianglan, Gottenberg, Jacques‐Eric, Anaya, Juan‐Manuel, Cunninghame‐Graham, Deborah S., Huang, Andrew J. W., Brennan, Michael T., Hughes, Pamela, Illei, Gabor G., Miceli‐Richard, Corinne, Keystone, Edward C., Bykerk, Vivian P., Hirschfield, Gideon, Xie, Gang, Ng, Wan‐Fai, Nordmark, Gunnel, Eriksson, Per, Omdal, Roald, Rhodus, Nelson L., Rischmueller, Maureen, Rohrer, Michael, Segal, Barbara M., Vyse, Timothy J., Wahren‐Herlenius, Marie, Witte, Torsten, Pons‐Estel, Bernardo, Alarcón‐Riquelme, Marta E., Guthridge, Joel M., James, Judith A., Lessard, Christopher J., Kelly, Jennifer A., Thompson, Susan D., Gaffney, Patrick M., Montgomery, Courtney G., Edberg, Jeffrey C., Kimberly, Robert P., Alarcón, Graciela S., Langefeld, Carl L., Gilkeson, Gary S., Kamen, Diane L., Tsao, Betty P., Joseph McCune, W., Salmon, Jane E., Merrill, Joan T., Weisman, Michael H., Wallace, Daniel J., Utset, Tammy O., Bottinger, Erwin P., Amos, Christopher I., Siminovitch, Katherine A., Mariette, Xavier, Sivils, Kathy L., Harley, John B., Hal Scofield, R.
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.05.2016)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.05.2016)
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Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
Norton, Mary E., Brar, Herb, Weiss, Jonathan, Karimi, Ardeshir, Laurent, Louise C., Caughey, Aaron B., Rodriguez, M. Hellen, Williams, John, Mitchell, Michael E., Adair, Charles D., Lee, Hanmin, Jacobsson, Bo, Tomlinson, Mark W., Oepkes, Dick, Hollemon, Desiree, Sparks, Andrew B., Oliphant, Arnold, Song, Ken
Published in American journal of obstetrics and gynecology (01.08.2012)
Published in American journal of obstetrics and gynecology (01.08.2012)
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Persons chronically exposed to low doses of ionizing radiation: A cytogenetic dosimetry study
Cherednichenko, Oksana, Pilyugina, Anastassiya, Nuraliev, Serikbai, Azizbekova, Dinara
Published in Mutation research. Genetic toxicology and environmental mutagenesis (01.02.2024)
Published in Mutation research. Genetic toxicology and environmental mutagenesis (01.02.2024)
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Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18
Sparks, Andrew B., Struble, Craig A., Wang, Eric T., Song, Ken, Oliphant, Arnold
Published in American journal of obstetrics and gynecology (01.04.2012)
Published in American journal of obstetrics and gynecology (01.04.2012)
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