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AUCD Experts

Omar Abdul-Rahman, MD

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Contact Information:
402-559-6328
Leadership:
Discipline Coordinators:
Genetics
Discipline(s):
Genetics/Genetic Counseling
AUCD Council Membership:
No Council Membership
Vita/Bio:
Service:
Linked Projects

Great Plains Health Callahan Cancer Center
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling Support Services
Nebraska Medicine Cardiovascular Genetcis
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine

Boy's Town Clinic
NE Methodist Hospital
Huntington's Disease Program
Children's Physicians
Children's Physicians
Boy's Town Clinic
Great Plains Health Callahan Cancer Center
Huntington's Disease Program
NE Methodist Hospital
Nebraska Medicine Cardiovascular Genetics
Nebraska Medicine Genetic Counseling Support Services
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine
Great Plains Health Callahan Cancer Center
Huntington's Disease Program
NE Methodist Hospital
Nebraska Medicine Cardiovascular Genetics
Nebraska Medicine Genetic Counseling Support Services
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine
Nebraska Medicine Ataxia Clinics
Boy's Town Clinic
Children's Physicians
June E Nylen Cancer Center
CHI Health Clinics - Inpatient Consultant
Boy's Town Clinic
Great Plains Health Callahan Cancer Center
Huntington's Disease Program
NE Methodist Hospital Inpatient and Perinatal
Nebraska Medicine Ataxia Clinics
Nebraska Medicine Cardiovascular Genetics
Nebraska Medicine Genetic Counseling Support Services
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine
Boy's Town Clinic
CHI Health Clinics - Inpatient Consultant
Children's Physicians
Great Plains Health Callahan Cancer Center
June E Nylen Cancer Center
NE Methodist Hospital Inpatient and Perinatal
Nebraska Medicine Ataxia Clinics
Nebraska Medicine Cardiovascular Genetics
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine
Boy's Town Clinic
CHI Health Clinics - Inpatient Consultant
Children's Physicians
Great Plains Health Callahan Cancer Center
June E Nylen Cancer Center
NE Methodist Hospital Inpatient and Perinatal
Nebraska Medicine Ataxia Clinics
Nebraska Medicine Cardiovascular Genetics
Nebraska Medicine Genetic Counseling- Cancer Genetics
Nebraska Medicine Genetic Counseling- Maternal Fetal Medicine
Linked Products

American Indian behavioral health focus of 2019 Great Plains Symposium at UNMC
Fetal Alcohol Spectrum Disorders: In London Medical Databases
Clinical and functional characteriztaion of recurrent missense variants implicated in THOC6-related intellectual disability.
An immune tolerance approach using transient low-dose methotrexate in the ERT-naive setting of patients treated with a therapeutic protein: experience in infantile-onset Pompe disease.
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.

Eliciting Narratives to Inform Care for Infants with Trisomy 18.
Patient with anomalous skin pigmentation expands the phenotype of ARID2 loss-of-function disorder, a SWI/SNF-related intellectual disability.
Vascular Dissection in Women with Turner Syndrome Cared for in the United States
Valve-Sparing Root and Total Arch Replacement for Cutis Laxa Aortopathy
PIGQ glycosylphosphatidylinositol-anchored protein deficiency: Characterizing the phenotype
Utilization of Echocardiography in Ehlers Danlos syndrome. Congenital Heart Disease
Expanding the Phenotype of MED13L Related Syndrome.
PTPN11 Duplication with a Noonan-like phenotype: a clinica report and literature review.
Cardinal Signs - Primrose Syndrome
Article
Article
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome
Fetal Akinesia with SCN4 lEU673Pro Variant: Second reported Case with detailed Phenotype Review
A Case Report of an Infant with Anauxetic Dysplasia and Severe Combined Immunodeficiency
Primrose Syndrome
Cytogenetics in Multiple Myeloma: Further Scrutiny of Deletions within the IGH Gene Region Enhances Risk Stratification
Reprogramming of Ovarian Granulosa Cells by YAP1 Leads to Development of High-Grade Cancer with Mesenchymal Lineage and Serous Features.
Fetal alcohol spectrum disorders: current state of diagnosis and treatment
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.
Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants With Suspected Genetic Disease: A Randomized Clinical Trial.
Noonan syndrome associated with focal occipital alopecia in a patient with RAF1 mutation: a case report and literature review
A Chief Medical Officer as Primary Supervisor: Experiences with a Commercial Payer
Genetic Testing Methodologies and Th Patient-Genetic Counselor Relationship
Clinical Variability in Patients With SMAD3 Aneurysm Osteoarthritis Syndrome