RobertJosephWallersteinMD

PubMed

• 1 citations
  Characteristics of Orofacial Clefting in Hawai'i.
  Lily Hoffman-Andrews, Jessica M Tarnowski, Sansan Lee, Lianne Hasegawa-Evans, Helen L Lau, Joan C Meister, Diane Lynne Ching, Robert Wallerstein> ;Hawai'i Journal of Health & Social Welfare. 2019 Aug 1
• 2 citations
  Prenatal presentation in a patient with Baraitser-Winter cerebrofrontofacial syndrome and a novel ACTB variant.
  Lila Aiyar, Tammy Stumbaugh, Greigh I. Hirata, Bruce Chen, Helen L Lau, Robert Wallerstein> ;Clinical Dysmorphology. 2019 Jul 1
• 13 citations
  Mosaic paternal genome-wide uniparental isodisomy with down syndrome.
  Diana Darcy, Paldeep S. Atwal, Cathy Angell, Inder K. Gadi, Robert Wallerstein> ;American Journal of Medical Genetics. Part A. 2015 Oct 1
• 13 citations
  Current knowledge of prenatal diagnosis of mosaic autosomal trisomy in amniocytes: karyotype/phenotype correlations
  Robert Wallerstein, Sonya Misra, R. Bryce Dugar, Monika Alem, Ronit Mazzoni, Matthew Garabedian> ;Prenatal Diagnosis. 2015 Sep 1
• 4 citations
  Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome.
  Kristen Dilzell, Diana Darcy, John Sum, Robert Wallerstein> ;Case Reports in Genetics. 2015 May 3
• 7 citations
  Familial congenital bilateral vocal fold paralysis: a novel gene translocation.
  Amy K Hsu, David E. Rosow, Robert Wallerstein, Max M. April> ;International Journal of Pediatric Otorhinolaryngology. 2015 Mar 1
• 8 citations
  Unusual Presentation of Pelizaeus-Merzbacher Disease: Female Patient with Deletion of the Proteolipid Protein 1 Gene
  Teva Brender, Donna Wallerstein, John Sum, Robert Wallerstein> ;Case Reports in Genetics. 2015 Feb 18
• 5 citations
  A New Model for Providing Cell-Free DNA and Risk Assessment for Chromosome Abnormalities in a Public Hospital Setting
  Robert Wallerstein, Andrea Jelks, Matthew Garabedian> ;Journal of Pregnancy. 2014 Jul 2
• 11 citations
  Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort.
  Ruey-Kang R. Chang, Yueh-Tze Lan, Michael J. Silka, Hallie Morrow, Alan Kwong, Janna Smith-Lang, Robert Wallerstein, Henry J. Lin> ;The Journal of Pediatrics. 2014 Mar 1
• 3 citations
  Antenatal detection of maternal unipartental disomy of chromosome 2 in a fetus with non-chromosomal, non-syndromic alobar holoprosencephaly
  Andrea Quintana, Matthew Garabedian, Robert Wallerstein> ;American Journal of Medical Genetics. Part A. 2014 Jan 1
• 2 citations
  Natural history of a child with Okamoto syndrome.
  Robert Wallerstein, Frances Rhoads> ;Clinical Dysmorphology. 2013 Jul 1
• 23 citations
  Deletion of 3p25.3 in a patient with intellectual disability and dysmorphic features with further definition of a critical region
  Gregory Kellogg, John Sum, Robert Wallerstein> ;American Journal of Medical Genetics. Part A. 2013 Jun 1
• 3 citations
  Pregnancy outcome in a woman with prune belly syndrome.
  R. Tyler Hillman, Matthew Garabedian, Robert Wallerstein> ;BMJ Case Reports. 2012 Nov 30
• 13 citations
  Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes.
  Matthew Garabedian, Donna F. Wallerstein, Nubia Medina, James Byrne, Robert J. Wallerstein> ;Case Reports in Genetics. 2012 Aug 28
• 10 citations
  Long‐term survival with diaphanospondylodysostosis (DSD): Survival to 5 years and further phenotypic characteristics
  Brian Scottoline, Scott Rosenthal, Rami Keisari, Rashmi Kirpekar, Cathy Angell, Robert Wallerstein> ;American Journal of Medical Genetics. Part A. 2012 Jun 1
• 9 citations
  Chromosome Deletion of 14q32.33 Detected by Array Comparative Genomic Hybridization in a Patient with Features of Dubowitz Syndrome
  Diana Darcy, Scott Rosenthal, Robert J. Wallerstein> ;Case Reports in Genetics. 2011 Sep 28
• 4 citations
  Microdeletion of chromosome 15q24.3-25.2 and orofacial clefting.
  Bindya Sing, Dongli Song, Glenn DeSandre, Balaji Govindaswami, Scott Rosenthal, Shelly Gunn, Robert J. Wallerstein> ;The Cleft Palate-Craniofacial Journal. 2011 Aug 29
• 48 citations
  Preconception care for women with diabetes and prevention of major congenital malformations.
  John L. Kitzmiller, Robert Wallerstein, Adolfo Correa, Saiyin Kwan> ;Birth Defects Research. Part A, Clinical and Molecular Teratology. 2010 Oct 1
• 3 citations
  Six year old with autoimmune polyglandular syndrome: can genetics tell us the story?
  Steven Ghanny, Robert Wallerstein, Amy Chartoff, Janet Post, Javier Aisenberg, Valerie Auyeung> ;Journal of Pediatric Endocrinology & Metabolism. 2010 Jul 1
• 3 citations
  A new case of MOMO syndrome.
  Robert Wallerstein, Rachel D. Sugalski> ;Clinical Dysmorphology. 2010 Jan 1
• 17 citations
  Copy number variations in three children with sudden infant death.
  Gokce Altay Toruner, Rohini Kurvathi, R. Sugalski, Lawrence N. Shulman, S. Twersky, P. G. Pearson, R. Tozzi, Marvin N. Schwalb, Robert J. Wallerstein> ;Clinical Genetics. 2009 Jul 1
• 4 citations
  The Role of Pediatricians in Families With a History of Familial Adenomatous Polyposis
  Ann Marie Augustyn, Robert Wallerstein> ;Clinical Pediatrics. 2009 Mar 31
• 46 citations
  Mutation analysis of B3GALTL in Peters Plus syndrome.
  Linda M. Reis, Rebecca C. Tyler, Omar A. Abdul-Rahman, Pamela Trapane, Robert Wallerstein, Diane Broome, Jodi D. Hoffman, Aneal Khan, Christina Paradiso, Nitin Ron, Am...> ;American Journal of Medical Genetics. Part A. 2008 Oct 15
• 2 citations
  Vascular malformations and upper extremity anomalies associated with a subtelomeric microdeletion of chromosome 4p.
  Roman Hossein Khonsari, Keith M. Blechman, Joe Michaels, Mordechai Vigler, David Chiu, Robert Wallerstein, Francine Blei> ;Clinical Dysmorphology. 2008 Jul 1
• 25 citations
  Expansion of the ARX spectrum.
  Robert Wallerstein, Rachel D. Sugalski, Leora Cohn, Robert Jawetz, Michael Friez> ;Clinical Neurology and Neurosurgery. 2008 Jun 1
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