Omar A Abdul-Rahman

Omar A Abdul-Rahman

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Omar A Abdul-Rahman

Omar A Abdul-Rahman

Publications by authors named "Omar A Abdul-Rahman"

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37Publications

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Computer-Aided Recognition of Facial Attributes for Fetal Alcohol Spectrum Disorders.

Pediatrics 2017 Dec;140(6)

Department of Genetic Medicine, Munroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, Nebraska

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http://dx.doi.org/10.1542/peds.2016-2028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703776PMC
December 2017

Congenital Amegakaryocytic Thrombocytopenia: A Case Series Indicating 2 Founder Variants in the Mississippi Band of Choctaw Indians.

J Pediatr Hematol Oncol 2017 10;39(7):573-575

*Department of Pediatrics, University of Mississippi Medical Center, Jackson †Choctaw Health Center, Philadelphia, MS.

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http://Insights.ovid.com/crossref?an=00043426-201710000-0001
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http://dx.doi.org/10.1097/MPH.0000000000000904DOI Listing
October 2017

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Authors:
Claire Redin Harrison Brand Ryan L Collins Tammy Kammin Elyse Mitchell Jennelle C Hodge Carrie Hanscom Vamsee Pillalamarri Catarina M Seabra Mary-Alice Abbott Omar A Abdul-Rahman Erika Aberg Rhett Adley Sofia L Alcaraz-Estrada Fowzan S Alkuraya Yu An Mary-Anne Anderson Caroline Antolik Kwame Anyane-Yeboa Joan F Atkin Tina Bartell Jonathan A Bernstein Elizabeth Beyer Ian Blumenthal Ernie M H F Bongers Eva H Brilstra Chester W Brown Hennie T Brüggenwirth Bert Callewaert Colby Chiang Ken Corning Helen Cox Edwin Cuppen Benjamin B Currall Tom Cushing Dezso David Matthew A Deardorff Annelies Dheedene Marc D'Hooghe Bert B A de Vries Dawn L Earl Heather L Ferguson Heather Fisher David R FitzPatrick Pamela Gerrol Daniela Giachino Joseph T Glessner Troy Gliem Margo Grady Brett H Graham Cristin Griffis Karen W Gripp Andrea L Gropman Andrea Hanson-Kahn David J Harris Mark A Hayden Rosamund Hill Ron Hochstenbach Jodi D Hoffman Robert J Hopkin Monika W Hubshman A Micheil Innes Mira Irons Melita Irving Jessie C Jacobsen Sandra Janssens Tamison Jewett John P Johnson Marjolijn C Jongmans Stephen G Kahler David A Koolen Jerome Korzelius Peter M Kroisel Yves Lacassie William Lawless Emmanuelle Lemyre Kathleen Leppig Alex V Levin Haibo Li Hong Li Eric C Liao Cynthia Lim Edward J Lose Diane Lucente Michael J Macera Poornima Manavalan Giorgia Mandrile Carlo L Marcelis Lauren Margolin Tamara Mason Diane Masser-Frye Michael W McClellan Cinthya J Zepeda Mendoza Björn Menten Sjors Middelkamp Liya R Mikami Emily Moe Shehla Mohammed Tarja Mononen Megan E Mortenson Graciela Moya Aggie W Nieuwint Zehra Ordulu Sandhya Parkash Susan P Pauker Shahrin Pereira Danielle Perrin Katy Phelan Raul E Piña Aguilar Pino J Poddighe Giulia Pregno Salmo Raskin Linda Reis William Rhead Debra Rita Ivo Renkens Filip Roelens Jayla Ruliera Patrick Rump Samantha L P Schilit Ranad Shaheen Rebecca Sparkes Erica Spiegel Blair Stevens Matthew R Stone Julia Tagoe Joseph V Thakuria Bregje W van Bon Jiddeke van de Kamp Ineke van Der Burgt Ton van Essen Conny M van Ravenswaaij-Arts Markus J van Roosmalen Sarah Vergult Catharina M L Volker-Touw Dorothy P Warburton Matthew J Waterman Susan Wiley Anna Wilson Maria de la Concepcion A Yerena-de Vega Roberto T Zori Brynn Levy Han G Brunner Nicole de Leeuw Wigard P Kloosterman Erik C Thorland Cynthia C Morton James F Gusella Michael E Talkowski

Nat Genet 2017 01 14;49(1):36-45. Epub 2016 Nov 14.

Molecular Neurogenetics Unit, Center for Human Genetic Research, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1038/ng.3720DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307971PMC
January 2017

A new leukocyte hyperadhesion syndrome of delayed cord separation, skin infection, and nephrosis.

Pediatrics 2014 Jan 16;133(1):e257-62. Epub 2013 Dec 16.

Division of Medical Genetics, Department of Pediatrics, University of Mississippi Medical Center, 2500 North State St, Jackson, MS 39216.

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http://dx.doi.org/10.1542/peds.2013-0884DOI Listing
January 2014

Neuromotor synapses in Escobar syndrome.

Am J Med Genet A 2013 Dec 16;161A(12):3042-8. Epub 2013 Aug 16.

Nemours Biomedical Research, Alfred I. duPont Hospital for Children, Wilmington, Delaware.

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http://dx.doi.org/10.1002/ajmg.a.36154DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600816PMC
December 2013

FOXP1 mutations cause intellectual disability and a recognizable phenotype.

Am J Med Genet A 2013 Dec 24;161A(12):3166-75. Epub 2013 Sep 24.

Hunter Genetics, Newcastle, NSW, Australia; John Hunter Children's Hospital, Newcastle, NSW, Australia.

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http://dx.doi.org/10.1002/ajmg.a.36174DOI Listing
December 2013

Prenatal diagnosis of congenital adrenal hyperplasia caused by P450 oxidoreductase deficiency.

J Clin Endocrinol Metab 2013 Mar 30;98(3):E528-36. Epub 2013 Jan 30.

Centre for Endocrinology, Diabetes, and Metabolism, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham B15 2TT, United Kingdom.

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http://dx.doi.org/10.1210/jc.2012-3449DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708032PMC
March 2013

An immunological basis of hyperphagia driven by GABAergic dysfunction in Prader-Willi Syndrome.

Med Hypotheses 2012 Apr 30;78(4):462-4. Epub 2012 Jan 30.

Department of Surgery, Physiology and Biophysics, The University of Mississippi Medical Center, Jackson, MS 39216-4505, USA.

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http://dx.doi.org/10.1016/j.mehy.2011.12.020DOI Listing
April 2012

Large contiguous gene deletions in Sjögren-Larsson syndrome.

Mol Genet Metab 2011 Nov 30;104(3):356-61. Epub 2011 May 30.

Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE 68198, USA.

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http://dx.doi.org/10.1016/j.ymgme.2011.05.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196763PMC
November 2011

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.

Am J Med Genet A 2011 Sep 10;155A(9):2186-95. Epub 2011 Aug 10.

Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710, USA.

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http://dx.doi.org/10.1002/ajmg.a.34226DOI Listing
September 2011

5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C.

Am J Med Genet A 2011 Jul 27;155A(7):1640-5. Epub 2011 May 27.

Department of Medicine, Methodist University Hospital/University of Tennessee Health Science Center, Memphis, 38104, USA.

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http://doi.wiley.com/10.1002/ajmg.a.34059
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http://dx.doi.org/10.1002/ajmg.a.34059DOI Listing
July 2011

Optic nerve enlargement in Krabbe disease: a pathophysiologic and clinical perspective.

J Child Neurol 2011 May 31;26(5):642-4. Epub 2011 Jan 31.

Center for Psychiatric Neuroscience, University of Mississippi Medical Center, Jackson, Mississippi 39216-4505, USA.

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http://dx.doi.org/10.1177/0883073810387929DOI Listing
May 2011

X-linked creatine transporter deficiency presenting as a mitochondrial disorder.

J Child Neurol 2010 Aug 25;25(8):1009-12. Epub 2010 May 25.

Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi, USA.

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http://dx.doi.org/10.1177/0883073809352109DOI Listing
August 2010

Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1beta.

J Pediatr Hematol Oncol 2009 Jul;31(7):527-9

Division of Medical Genetics, Department of Pediatrics, University of Mississippi Medical Center, Jackson, MS, USA.

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http://dx.doi.org/10.1097/MPH.0b013e3181a974c8DOI Listing
July 2009

Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblings.

Neurol Sci 2008 Dec 27;29(6):467-70. Epub 2008 Nov 27.

Department of Neurosurgery, University of Mississippi Medical Center, 2500 N. State Street, Jackson, MS, 39216-4505, USA.

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http://link.springer.com/10.1007/s10072-008-1016-0
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http://dx.doi.org/10.1007/s10072-008-1016-0DOI Listing
December 2008

Van den Ende-Gupta syndrome: laryngeal abnormalities in two siblings.

Am J Med Genet A 2007 Nov;143A(22):2706-11

Division of Medical Genetics, Department of Preventive Medicine, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.

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http://dx.doi.org/10.1002/ajmg.a.32007DOI Listing
November 2007

Genitopatellar syndrome: expanding the phenotype and excluding mutations in LMX1B and TBX4.

Am J Med Genet A 2006 Jul;140(14):1567-72

Division of Medical Genetics, Department of Preventive Medicine, University of Mississippi Medical Center, Jackson, MS 39216, USA.

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http://dx.doi.org/10.1002/ajmg.a.31258DOI Listing
July 2006

The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders.

Genet Med 2006 Jan;8(1):50-4

Division of Medical Genetics, Department of Pediatrics, Stanford University, 300 Pasteur Drive, H-315, Stanford, CA 94305, USA.

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http://dx.doi.org/10.109701.gim.0000195304.45116.96DOI Listing
January 2006

Cryptococcal sepsis diagnosed by bone marrow examination.

J Pediatr Hematol Oncol 2004 Aug;26(8):526-8

Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.

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http://dx.doi.org/10.1097/01.mph.0000130218.49155.09DOI Listing
August 2004