28120936 | Create Study | Potential molecular consequences of transgene integration: The R6/2 mouse example. | Scientific reports | Jacobsen, Jessie C; Erdin, Serkan; Chiang, Colby; Hanscom, Carrie; Handley, Renee R; Barker, Douglas D; Stortchevoi, Alex; Blumenthal, Ian; Reid, Suzanne J; Snell, Russell G; MacDonald, Marcy E; Morton, A Jennifer; Ernst, Carl; Gusella, James F; Talkowski, Michael E | January 2017 | Not Determined |
25497101 | Create Study | Genomic and functional overlap between somatic and germline chromosomal rearrangements. | Cell reports | van Heesch S, Simonis M, van Roosmalen MJ, Pillalamarri V, Brand H, Kuijk EW, de Luca KL, Lansu N, Braat AK, Menelaou A, Hao W, Korving J, Snijder S, van der Veken LT, Hochstenbach R, Knegt AC, Duran K, Renkens I, Alekozai N, Jager M, Vergult S, Menten B, de Bruijn E, Boymans S, Ippel E, et al. | December 24, 2014 | Not Relevant |
24789519 | Create Study | Design of large-insert jumping libraries for structural variant detection using Illumina sequencing. | Current protocols in human genetics | Hanscom, C; Talkowski, M | January 2014 | Not Determined |
24746958 | Create Study | Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature. | American journal of human genetics | Ordulu, Zehra; Wong, Kristen E; Currall, Benjamin B; Ivanov, Andrew R; Pereira, Shahrin; Althari, Sara; Gusella, James F; Talkowski, Michael E; Morton, Cynthia C | May 1, 2014 | Not Relevant |
23472757 | Create Study | Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs. | American journal of human genetics | Chen, Xiaoli; Shen, Yiping; Zhang, Feng; Chiang, Colby; Pillalamarri, Vamsee; Blumenthal, Ian; Talkowski, Michael; Wu, Bai-Lin; Gusella, James F | March 7, 2013 | Not Relevant |
23354975 | Create Study | Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate. | Human genetics | Lindgren, Amelia M; Hoyos, Tatiana; Talkowski, Michael E; Hanscom, Carrie; Blumenthal, Ian; Chiang, Colby; Ernst, Carl; Pereira, Shahrin; Ordulu, Zehra; Clericuzio, Carol; Drautz, Joanne M; Rosenfeld, Jill A; Shaffer, Lisa G; Velsher, Lea; Pynn, Tania; Vermeesch, Joris; Harris, David J; Gusella, James F; Liao, Eric C; Morton, Cynthia C | May 2013 | Not Relevant |
23332918 | Create Study | Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. | American journal of human genetics | Beunders, Gea; Voorhoeve, Els; Golzio, Christelle; Pardo, Luba M; Rosenfeld, Jill A; Talkowski, Michael E; Simonic, Ingrid; Lionel, Anath C; Vergult, Sarah; Pyatt, Robert E; van de Kamp, Jiddeke; Nieuwint, Aggie; Weiss, Marjan M; Rizzu, Patrizia; Verwer, Lucilla E N I; van Spaendonk, Rosalina M L; Shen, Yiping; Wu, Bai-lin; Yu, Tingting; Yu, Yongguo; Chiang, Colby; Gusella, James F; Lindgren, Amelia M; Morton, Cynthia C; van Binsbergen, Ellen; Bulk, Saskia; van Rossem, Els; Vanakker, Olivier; Armstrong, Ruth; Park, Soo-Mi; Greenhalgh, Lynn; Maye, Una; Neill, Nicholas J; Abbott, Kristin M; Sell, Susan; Ladda, Roger; Farber, Darren M; Bader, Patricia I; Cushing, Tom; Drautz, Joanne M; Konczal, Laura; Nash, Patricia; de Los Reyes, Emily; Carter, Melissa T; Hopkins, Elizabeth; Marshall, Christian R; Osborne, Lucy R; Gripp, Karen W; Thrush, Devon Lamb; Hashimoto, Sayaka; Gastier-Foster, Julie M; Astbury, Caroline; Ylstra, Bauke; Meijers-Heijboer, Hanne; Posthuma, Danielle; Menten, Björn; Mortier, Geert; Scherer, Stephen W; Eichler, Evan E; Girirajan, Santhosh; Katsanis, Nicholas; Groffen, Alexander J; Sistermans, Erik A | February 7, 2013 | Not Relevant |
23217328 | Create Study | Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities. | American journal of human genetics | Talkowski, Michael E; Maussion, Gilles; Crapper, Liam; Rosenfeld, Jill A; Blumenthal, Ian; Hanscom, Carrie; Chiang, Colby; Lindgren, Amelia; Pereira, Shahrin; Ruderfer, Douglas; Diallo, Alpha B; Lopez, Juan Pablo; Turecki, Gustavo; Chen, Elizabeth S; Gigek, Carolina; Harris, David J; Lip, Va; An, Yu; Biagioli, Marta; Macdonald, Marcy E; Lin, Michael; Haggarty, Stephen J; Sklar, Pamela; Purcell, Shaun; Kellis, Manolis; Schwartz, Stuart; Shaffer, Lisa G; Natowicz, Marvin R; Shen, Yiping; Morton, Cynthia C; Gusella, James F; Ernst, Carl | December 7, 2012 | Not Determined |
23215558 | Create Study | Clinical diagnosis by whole-genome sequencing of a prenatal sample. | The New England journal of medicine | Talkowski, Michael E; Ordulu, Zehra; Pillalamarri, Vamsee; Benson, Carol B; Blumenthal, Ian; Connolly, Susan; Hanscom, Carrie; Hussain, Naveed; Pereira, Shahrin; Picker, Jonathan; Rosenfeld, Jill A; Shaffer, Lisa G; Wilkins-Haug, Louise E; Gusella, James F; Morton, Cynthia C | December 6, 2012 | Not Relevant |
23044507 | Create Study | Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. | Archives of general psychiatry | Ernst C, Marshall CR, Shen Y, Metcalfe K, Rosenfeld J, Hodge JC, Torres A, Blumenthal I, Chiang C, Pillalamarri V, Crapper L, Diallo AB, Ruderfer D, Pereira S, Sklar P, Purcell S, Wildin RS, Spencer AC, Quade BF, Harris DJ, Lemyre E, Wu BL, Stavropoulos DJ, Geraghty MT, Shaffer LG, et al. | December 2012 | Not Determined |
22770980 | Create Study | Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies. | American journal of human genetics | Kim, Hyung-Goo; Kim, Hyun-Taek; Leach, Natalia T; Lan, Fei; Ullmann, Reinhard; Silahtaroglu, Asli; Kurth, Ingo; Nowka, Anja; Seong, Ihn Sik; Shen, Yiping; Talkowski, Michael E; Ruderfer, Douglas; Lee, Ji-Hyun; Glotzbach, Caron; Ha, Kyungsoo; Kjaergaard, Susanne; Levin, Alex V; Romeike, Bernd F; Kleefstra, Tjitske; Bartsch, Oliver; Elsea, Sarah H; Jabs, Ethylin Wang; MacDonald, Marcy E; Harris, David J; Quade, Bradley J; Ropers, Hans-Hilger; Shaffer, Lisa G; Kutsche, Kerstin; Layman, Lawrence C; Tommerup, Niels; Kalscheuer, Vera M; Shi, Yang; Morton, Cynthia C; Kim, Cheol-Hee; Gusella, James F | July 13, 2012 | Not Determined |
22521361 | Create Study | Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. | Cell | Talkowski, Michael E; Rosenfeld, Jill A; Blumenthal, Ian; Pillalamarri, Vamsee; Chiang, Colby; Heilbut, Adrian; Ernst, Carl; Hanscom, Carrie; Rossin, Elizabeth; Lindgren, Amelia M; Pereira, Shahrin; Ruderfer, Douglas; Kirby, Andrew; Ripke, Stephan; Harris, David J; Lee, Ji-Hyun; Ha, Kyungsoo; Kim, Hyung-Goo; Solomon, Benjamin D; Gropman, Andrea L; Lucente, Diane; Sims, Katherine; Ohsumi, Toshiro K; Borowsky, Mark L; Loranger, Stephanie; Quade, Bradley; Lage, Kasper; Miles, Judith; Wu, Bai-Lin; Shen, Yiping; Neale, Benjamin; Shaffer, Lisa G; Daly, Mark J; Morton, Cynthia C; Gusella, James F | April 27, 2012 | Not Relevant |
22388000 | Create Study | Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration. | Nature genetics | Chiang C, Jacobsen JC, Ernst C, Hanscom C, Heilbut A, Blumenthal I, Mills RE, Kirby A, Lindgren AM, Rudiger SR, McLaughlan CJ, Bawden CS, Reid SJ, Faull RL, Snell RG, Hall IM, Shen Y, Ohsumi TK, Borowsky ML, Daly MJ, Lee C, Morton CC, MacDonald ME, Gusella JF, Talkowski ME | April 2012 | Not Relevant |
22290657 | Create Study | Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features. | Human mutation | Lamb, Allen N; Rosenfeld, Jill A; Neill, Nicholas J; Talkowski, Michael E; Blumenthal, Ian; Girirajan, Santhosh; Keelean-Fuller, Debra; Fan, Zheng; Pouncey, Jill; Stevens, Cathy; Mackay-Loder, Loren; Terespolsky, Deborah; Bader, Patricia I; Rosenbaum, Kenneth; Vallee, Stephanie E; Moeschler, John B; Ladda, Roger; Sell, Susan; Martin, Judith; Ryan, Shawnia; Jones, Marilyn C; Moran, Rocio; Shealy, Amy; Madan-Khetarpal, Suneeta; McConnell, Juliann; Surti, Urvashi; Delahaye, Andrée; Heron-Longe, Bénédicte; Pipiras, Eva; Benzacken, Brigitte; Passemard, Sandrine; Verloes, Alain; Isidor, Bertrand; Le Caignec, Cedric; Glew, Gwen M; Opheim, Kent E; Descartes, Maria; Eichler, Evan E; Morton, Cynthia C; Gusella, James F; Schultz, Roger A; Ballif, Blake C; Shaffer, Lisa G | April 2012 | Not Determined |
21981781 | Create Study | Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. | American journal of human genetics | Talkowski, Michael E; Mullegama, Sureni V; Rosenfeld, Jill A; van Bon, Bregje W M; Shen, Yiping; Repnikova, Elena A; Gastier-Foster, Julie; Thrush, Devon Lamb; Kathiresan, Sekar; Ruderfer, Douglas M; Chiang, Colby; Hanscom, Carrie; Ernst, Carl; Lindgren, Amelia M; Morton, Cynthia C; An, Yu; Astbury, Caroline; Brueton, Louise A; Lichtenbelt, Klaske D; Ades, Lesley C; Fichera, Marco; Romano, Corrado; Innis, Jeffrey W; Williams, Charles A; Bartholomew, Dennis; Van Allen, Margot I; Parikh, Aditi; Zhang, Lilei; Wu, Bai-Lin; Pyatt, Robert E; Schwartz, Stuart; Shaffer, Lisa G; de Vries, Bert B A; Gusella, James F; Elsea, Sarah H | October 7, 2011 | Not Relevant |
21473983 | Create Study | Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research. | American journal of human genetics | Talkowski, Michael E; Ernst, Carl; Heilbut, Adrian; Chiang, Colby; Hanscom, Carrie; Lindgren, Amelia; Kirby, Andrew; Liu, Shangtao; Muddukrishna, Bhavana; Ohsumi, Toshiro K; Shen, Yiping; Borowsky, Mark; Daly, Mark J; Morton, Cynthia C; Gusella, James F | April 8, 2011 | Not Relevant |