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Samin A. Sajan, Ph.D. - Publications

Affiliations: 
2008 Washington University, Saint Louis, St. Louis, MO 
Area:
Genetics
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Sajan SA, Brown CM, Davis-Keppen L, Burns K, Royer E, Coleman JAC, Hilton BA, DuPont BR, Perry DL, Taft RJ, Kesari A. The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex development. American Journal of Medical Genetics. Part A. PMID 37551848 DOI: 10.1002/ajmg.a.63367  0.319
2018 Sajan SA, Ganesh J, Shinde DN, Powis Z, Scarano MI, Stone J, Winter S, Tang S. Biallelic disruption of is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic features. Journal of Medical Genetics. PMID 30478137 DOI: 10.1136/Jmedgenet-2018-105639  0.433
2018 Farwell Hagman KD, Shinde DN, Mroske C, Smith E, Radtke K, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Alcaraz WA, Helbig KL, Sajan SA, Rossi M, Lu HM, Huether R, et al. Erratum: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29388939 DOI: 10.1038/gim.2017.263  0.304
2011 Sajan SA, Rubenstein JL, Warchol ME, Lovett M. Identification of direct downstream targets of Dlx5 during early inner ear development. Human Molecular Genetics. 20: 1262-73. PMID 21227998 DOI: 10.1093/Hmg/Ddq567  0.684
2010 Sajan SA, Waimey KE, Millen KJ. Novel approaches to studying the genetic basis of cerebellar development. Cerebellum (London, England). 9: 272-83. PMID 20387026 DOI: 10.1007/s12311-010-0169-6  0.315
2007 Sajan SA, Warchol ME, Lovett M. Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysis. Genetics. 177: 631-53. PMID 17660535 DOI: 10.1534/Genetics.107.078584  0.715
2007 Hawkins RD, Bashiardes S, Powder KE, Sajan SA, Bhonagiri V, Alvarado DM, Speck J, Warchol ME, Lovett M. Large scale gene expression profiles of regenerating inner ear sensory epithelia. Plos One. 2: e525. PMID 17565378 DOI: 10.1371/Journal.Pone.0000525  0.35
2006 Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, Murray JC, Schutte BC. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature Genetics. 38: 1335-40. PMID 17041601 DOI: 10.1038/Ng1903  0.56
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