Toward a Systems Biology of Mouse Inner Ear Organogenesis: Gene Expression Pathways, Patterns and Network Analysis

Por Sajan, Samin A., Warchol, Mark E., Lovett, Michael
Publicado em 2007

Novel Approaches to Studying the Genetic Basis of Cerebellar Development

Por Sajan, Samin A., Waimey, Kathryn E., Millen, Kathleen J.
Publicado em 2010

Identification of direct downstream targets of Dlx5 during early inner ear development

Por Sajan, Samin A., Rubenstein, John L.R., Warchol, Mark E., Lovett, Michael
Publicado em 2011

Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia

Por Hawkins, R. David, Bashiardes, Stavros, Powder, Kara E., Sajan, Samin A., Bhonagiri, Veena, Alvarado, David M., Speck, Judith, Warchol, Mark E., Lovett, Michael
Publicado em 2007

Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption

Por Paciorkowski, Alex R, Keppler-Noreuil, Kim, Robinson, Luther, Sullivan, Christopher, Sajan, Samin, Christian, Susan L, Bukshpun, Polina, Gabriel, Stacy B, Gleeson, Joseph G, Sherr, Elliott H, Dobyns, William B
Publicado em 2013

Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

Por Ingraham, Christopher R, Kinoshita, Akira, Kondo, Shinji, Yang, Baoli, Sajan, Samin, Trout, Kurt J, Malik, Margaret I, Dunnwald, Martine, Goudy, Stephen L, Lovett, Michael, Murray, Jeffrey C, Schutte, Brian C
Publicado em 2006

Enrichment of mutations in chromatin regulators in people with Rett Syndrome lacking mutations in MECP2

Por Sajan, Samin A., Jhangiani, Shalini N., Muzny, Donna M., Gibbs, Richard A., Lupski, James R., Glaze, Daniel G., Kaufmann, Walter E., Skinner, Steven A., Anese, Fran, Friez, Michael J., Jane, Lane, Percy, Alan K., Neul, Jeffrey L.
Publicado no Genet Med (2016)

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

Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline

Por Hardies, Katia, Cai, Yiying, Jardel, Claude, Jansen, Anna C., Cao, Mian, May, Patrick, Djémié, Tania, Hachon Le Camus, Caroline, Keymolen, Kathelijn, Deconinck, Tine, Bhambhani, Vikas, Long, Catherine, Sajan, Samin A., Helbig, Katherine L., Suls, Arvid, Balling, Rudi, Helbig, Ingo, De Jonghe, Peter, Depienne, Christel, De Camilli, Pietro, Weckhuysen, Sarah
Publicado no Brain (2016)

Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases

Por Farwell Hagman, Kelly D., Shinde, Deepali N., Mroske, Cameron, Smith, Erica, Radtke, Kelly, Shahmirzadi, Layla, El-Khechen, Dima, Powis, Zöe, Chao, Elizabeth C., Alcaraz, Wendy A., Helbig, Katherine L., Sajan, Samin A., Rossi, Mari, Lu, Hsiao-Mei, Huether, Robert, Li, Shuwei, Wu, Sitao, Nuñes, Mark E., Tang, Sha
Publicado no Genet Med (2017)