Coincidence of P-Insertion Sites and Breakpoints of Deletions Induced by Activating P Elements in Drosophila

Por Sudi, Jyotsna, Zhang, Sen, Intrieri, Gino, Hao, Ximing, Zhang, Ping
Publicado em 2008

Duplication 16p11.2 in a Child with Infantile Seizure Disorder

Por Bedoyan, Jirair K., Kumar, Ravinesh A., Sudi, Jyotsna, Silverstein, Faye, Ackley, Todd, Iyer, Ramaswamy K., Christian, Susan L., Martin, Donna M.
Publicado em 2010

Genome-Wide Methylation Study Identifies an IL-13–induced Epigenetic Signature in Asthmatic Airways

Por Nicodemus-Johnson, Jessie, Naughton, Katherine A., Sudi, Jyotsna, Hogarth, Kyle, Naurekas, Edward T., Nicolae, Dan L., Sperling, Anne I., Solway, Julian, White, Steven R., Ober, Carole
Publicado no Am J Respir Crit Care Med (2016)

Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females

Por Marsh, Eric, Fulp, Carl, Gomez, Ernest, Nasrallah, Ilya, Minarcik, Jeremy, Sudi, Jyotsna, Christian, Susan L., Mancini, Grazia, Labosky, Patricia, Dobyns, William, Brooks-Kayal, Amy, Golden, Jeffrey A.
Publicado em 2009

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

Por Kumar, Ravinesh A, Sudi, Jyotsna, Babatz, Timothy D, Brune, Camille W, Oswald, Donald, Yen, Mayon, Nowak, Norma J, Cook, Edwin H, Christian, Susan L, Dobyns, William B
Publicado em 2009

Microcephaly, sensorineural deafness and Currarino triad with duplication–deletion of distal 7q

Por Pavone, Piero, Ruggieri, Martino, Lombardo, Ilaria, Sudi, Jyotsna, Biancheri, Roberta, Castellano-Chiodo, Danilo, Rossi, Andrea, Incorpora, Gemma, Nowak, Norma J., Christian, Susan L., Pavone, Lorenzo, Dobyns, William B.
Publicado em 2009

Maternal asthma and microRNA regulation of soluble HLA-G in the airway.

Por Nicodemus-Johnson, Jessie, Laxman, Bharathi, Stern, Randi K., Sudi, Jyotsna, Tierney, Courtney N., Norwick, Lourdes, Hogarth, Douglas K., McConville, John F., Naureckas, Edward T., Sperling, Anne I., Solway, Julian, Krishnan, Jerry A., Nicolae, Dan L., White, Steven R., Ober, Carole
Publicado em 2013

Novel Submicroscopic chromosomal abnormalities detected in Autism Spectrum Disorder

Por Christian, Susan L., Brune, Camille W., Sudi, Jyotsna, Kumar, Ravinesh A., Liu, Shaung, KaraMohamed, Samer, Badner, Judith A., Matsui, Seiichi, Conroy, Jeffrey, McQuaid, Devin, Gergel, James, Hatchwell, Eli, Gilliam, T. Conrad, Gershon, Elliot S., Nowak, Norma J., Dobyns, William B., Cook, Edwin H.
Publicado em 2008

Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

Por Kumar, Ravinesh A., Marshall, Christian R., Badner, Judith A., Babatz, Timothy D., Mukamel, Zohar, Aldinger, Kimberly A., Sudi, Jyotsna, Brune, Camille W., Goh, Gerald, KaraMohamed, Samer, Sutcliffe, James S., Cook, Edwin H., Geschwind, Daniel H., Dobyns, William B., Scherer, Stephen W., Christian, Susan L.
Publicado em 2009

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

Por Sajan, Samin A., Fernandez, Liliana, Nieh, Sahar Esmaeeli, Rider, Eric, Bukshpun, Polina, Wakahiro, Mari, Christian, Susan L., Rivière, Jean-Baptiste, Sullivan, Christopher T., Sudi, Jyotsna, Herriges, Michael J., Paciorkowski, Alexander R., Barkovich, A. James, Glessner, Joseph T., Millen, Kathleen J., Hakonarson, Hakon, Dobyns, William B., Sherr, Elliott H.
Publicado em 2013