Professor, Pediatrics, Medical College of Wisconsin

Medical Genetics

David Bick practices Medical Genetics. He went to George Washington University School of Medicine. George Washington University School of Medicine has a rank of 67 in research and a 0 in primary care David Bick is also a published physician. He has 50 publication published. The most recent publication is: Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism.

Publications

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• Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.
• High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phen...
• Ethical Issues in DNA Sequencing in the Neonate.
• In the absence of evidentiary harm, existing societal norms regarding parental authority should prevail.
• Views of Primary Care Providers Regarding the Return of Genome Sequencing Incidental Findings.
• Genomics in clinical practice: lessons from the front lines.
• AKT1 Gene Mutation Levels Are Correlated with the Type of Dermatologic Lesions in Patients with Proteus Syndrome.
• A simplified method for screening siblings for HLA identity using short tandem repeat (STR) polymorphisms.
• Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study.
• The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
• Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
• Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
• A timely arrival for genomic medicine.
• WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
• Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
• Preimplantation HLA haplotyping using tri-, tetra-, and pentanucleotide short tandem repeats for HLA matching.
• Preimplantation genetic diagnosis.
• Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.
• Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization.
• The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism.
• Birth of a healthy infant following preimplantation PKHD1 haplotyping for autosomal recessive polycystic kidney disease using multiple displacement amplification.
• Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadism.
• The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
• Zoom-in comparative genomic hybridisation arrays for the characterisation of variable breakpoint contiguous gene syndromes.
• KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans.
• Mutation analysis of the EMX2 gene in Kallmann's syndrome.
• Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay.
• Is it the patient or the IVF? Beckwith-Wiedemann syndrome in both spontaneous and assisted reproductive conceptions.
• Whole exome and whole genome sequencing.
• Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism.
• Preimplantation genetic diagnosis: technology and clinical applications.
• Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome.
• A Mosaic Activating Mutation in AKT1 Associated with the Proteus Syndrome.
• Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome.
• Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletion.
• Prenatal diagnosis and investigation of a fetus with chondrodysplasia punctata, ichthyosis, and Kallmann syndrome due to an Xp deletion.
• Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
• Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism.
• Chromosome abnormalities in and pathogenesis of Kallmann syndrome.
• Successful congenital heart surgery for a toddler with idiopathic infantile arterial calcification.
• Preimplantation genetic diagnosis for spinal muscular atrophy type I.
• Ontogeny of growth-regulating genes in the placenta.
• Screening for cystic fibrosis carriers.
• Differential expression of novel Gs alpha signal transduction protein cDNA species.
• Improved sizing of fragile X CCG repeats by nested polymerase chain reaction.
• Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies.
• Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease.
• DNA-based prenatal determination of the RhEe genotype.
• Prenatal screening for delta F508 mutation in population not selected for cystic fibrosis.

Schools

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• George Washington University

• Yale New Haven Hospital

Doctors Specialties

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• Clinical Molecular Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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Education

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• Yale New Haven Children's Center
• Yale-New Haven Hospital
• George Washington University School of Medicine

Hospital

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• Children's Hospital of Wisconsin

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