DavidPBickMD

PubMed

• 60 citations
  Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and ...
  Catherine Rehder, Lora J. H. Bean, David P. Bick, Elizabeth C. Chao, Wendy K. Chung
  Genetics in Medicine. 2021-04-29
• 103 citations
  Whole exome and whole genome sequencing.
  David P. Bick, David Dimmock
  Current Opinion in Pediatrics. 2011-12-01
• 369 citations
  Implementing genomic medicine in the clinic: the future is here
  Teri A. Manolio, Rex L. Chisholm, Brad Ozenberger, Dan M. Roden, Marc S. Williams
  Genetics in Medicine. 2013-01-10

Journal Articles

• Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States  
  Miller, M.J., Burrage, L.C., Gibson, J.B., Strenk, M.E., Lose, E.J., Bick, D.P., Elsea, S.H., Sutton, V.R., Sun, Q., Graham, B.H., Craigen, W.J., Zhang, V.W., Wong, L.C., Molecular Genetics and Metabolism, 1/1/2015
• Ehtical issues in DNA sequencing in the neonate  
  Dimmock, D.P., Bick, D.P., Clin Perinatol, 1/1/2014
• Whole exome analysis identifies dominant COL4A1 mutations in patients with complex ocular phenotypes involving microphthalmia  
  Deml, B., Reis, L., Maheshwarti, M., Griffis, C., BICK, D., Semina, E., Clin Genet, 1/1/2014
• Views of nonmedical, health system professionals regarding the return of whole genome sequencing incidental findings  
  Strong, A., Zusevics. L., Bick, D.P., Veith, R., WMJ, 1/1/2014
• Novel B3GALTL mutations in classic Peters Plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes  
  Weh, E., Reis, L.M., Tyler, R.C., Bick, D.P., Rhead, W.J., Wallace, S., McGregor, T.L., Dills, S.K., Chao, M.C., Murray, J.C., Semina, E.V., Clin Genet, 1/24/2013
• AKT1 gene mutation levels are correlated with the type of dermatologic lesions in patients with Proteus syndrome  
  Lindhurst, M.J., Wang, J., Bloomhardt, H., Wikowski, A.M. Singh, L.N., Bick, D.P., Gambello, M.J., Powerll, C.M. Chia, C., Lee, R., Darling, T.N. Biesecker, L.G., J Invest Dermatol, 1/24/2013
• A simplified method for screening siblings for HLA identity using short tandem repeat (STR) polymorphims  
  Schiller, J.J., Hopp, K.A., Peitz, B.C., Bick, D.P., Lau, E.C., Ellis, T.M., Human Immun, 1/20/2013
• Implementing genomic medicine in the clinic: the future is here  
  Manolio, T.A., Chisholm, R.L., Ozenberger, B., Roden, D.M., Marc S. Williams, M.S., Wilson, R., BICK, D., et al, Genet Med, 1/1/2013
• Assuring the quality of next-generation sequencing in clinical laboratory practice  
  Gargis, A.S., Kalman, L., Berry, M.W., Bick, D.P., Dimmock, D.P., Hambuch, T., Lu, F., Lyon, E., Voelkerding, K.V., Zehnbauer, B.A., Agarwala, R., Bennett, S.F., Chen,..., Nat Biotechnol, 1/30/2012
• Human gene copy number spectra analysis in congenital heart malformations  
  Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, BICK DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME, Physiol Genomics, 1/1/2012
• Making a definitive diagnosis: Successful clinical application of whole genome sequencing in a child with intractable inflammatory bowel disease  
  Worthey, E.A., Mayer, A.N., Syverson, G.D., Helbling, D., Bonacci, B.B., Decker, B., Serpe, J.M., Dasu, T., Tschannen, M.R., Veith, R.L., Basehore, M.J., Broeckel, U.,..., Gen Med, 1/1/2011
• mosaic activating mutation in AKT1 associated with the Proteus syndrome  
  Lindhurst, M.J., Sapp, J.C., Teer, J.K., Johnston, J.J., Finn, E.M., Peters, K., Turner, J., Cannons, J.L., BICK, D., Blakemore, L., Blumhorst, C., Brockmann, K., Cald..., N Engl J Med, 1/1/2011
• A timely arrival for genomic medicine  
  Mayer, A.N., Dimmock, D.P., Arca, M.J., Bick, D.P., Verbsky, J.W., Worthey, E.A., Jacob, H.J., Margolis, D.A., Gen Med, 1/1/2011
• Birth of a healthy infant following preimplantation PKHD1 halotyping for autosomal recessive polycystic kidney disease using multiple displacement amplification  
  Lau, E.C., Janson, M.M., Roesler, M.R., Avner, E. D., Strawn, E.Y., Bick, D.P., J Ass Repro Gen, 1/1/2010
• Mutations in CHD7, encoding a chromatin remodeling protein, cause idiopathic hpogonadotropic hypogonadism and Kallman syndrome  
  Kim, H.G., Kurth, I., Lan, F., Meliciani, I., Wenzel, W., Eom, S.H., Kang, G.B., Rosenberger, G., Tekin, M., Metin, O., Bick, D.P., Sherins, R., Walker, S., Shi, Y., G..., Am J of Hum Genet, 1/1/2008
• Preimplantation Genetic Diagnosis: Technology and Clinical Applications  
  Swanson, A., Strawn, E., Lau, E., BICK, D., Wis Med J, 1/1/2007
• Zoom-in CGH arrays for the characterization of variable breakpoint contiguous gene syndromes  
  Johnston, J.J., Walker, R.L., Davis, S., Facio, F., Turner, J.T., Bick, D.P., Daentl, D.L., Ellison, J.W., Meltzer, P.S., Biesecker, L.G., J Med Genet, 1/1/2007
• Clinical and molecular characterization of a large sample of patients with hypogonadotrophic hypogonadism  
  Bhagavath, B., Podolsky, R.H., Ozata, M., Bolu, E., Bick, D.P., Kulharya, A., Sherins, R.J., Layman, L.C., Fertil Steril, 1/1/2006
• Interstitial deletion of chromosome 12q: Genotype-Phenotype correlation of two patients utilizing array comparative genomic hybridization  
  Klein, O.D., Cotter, P.D., Schmidt, A.M., BICK, D.P., Tidyma, W.I., Albertson, D.G., Pinkel, D., Rauen, K.A., Am J Med Genet, 1/1/2005
• Analysis of the PROP1 gene in a large sample of patients with idiopathic hypogonadotropic hypogonadism  
  Park J.K., Ozata M., Chorich L.P., Cheng L., Bick, D.P., Sherins R.J., Ozdemir I.C., Cogan J, Phillips J.A. III, Layman L.C., Clin Endocrinol (Oxf), 1/1/2004
• Short Communication: Prenatal diagnosis of Smith-Lemli-Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex-reversed fetus  
  BICK, D.B., McCorkle, D., Stanley, W.S., Stern, H.J., Staszak, P., Berkovitz, G.D., Meyers, C.M., Kelley, R.I., Prenat Diagn, 1/1/1999
• Semen donor screening for hereditary diseases: The Fairfax Cryobank Experience  
  Bick, D.P., Fugger, E.F., Pool, S., Hazelrigg, W.B., Yadvish, K.N., Spence, W.C., Maddalena, A., Howard-Peebles, P.N., Schulman, J.D., J Reprod Med, 1/1/1998
• Molecular fragile X screening in normal populations  
  Spence, W.C., Black, S.H., Fallon, L., Maddalena, A., Cummings, E., Menapace-Drew, G., Bick, D.P., Levinson, G., Schulman, J.D., Howard-Peebles, P.N., Am J Med Genet, 1/1/1996
• Genetic disease diagnosis: Challenges and opportunities  
  Bick, D.P., IEEE Engineering in Medicine and Biology Magazine, 1/1/1995
• Fragile X screening in pediatric & obstetrical patients  
  Howard-Peebles, P.N., Maddalena, A., Black, S.H., Levinson, G., Bick, D.P.. Schulman, J.D., Dev Brain Dysfunct, 1/1/1995
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Books/Book Chapters

• Vitro Fertilization: Innovative Clinical and Laboratory Aspects 
  Chapter: Preimplantation Genetic Testing: Current Status and Future Prospects 
  Lau, E.C., Janson, M.M., Ball, C.B., Roesler M.R., VanTuinen, P., Bick, D.P., Strawn, E.Y.2012

Abstracts/Posters

• Intragenic SCN1A microdeletion in a patient with infantile-onset epilepsy highlights the range and limitations of microarrays and DNA sequencing.
  Bick, D.P., ACMG Annual Meeting, Salt Lake City, UT, 1/1/2015
• AKT1 gene mutation levels are correlated with the type of dermatologic lesions in patients with Proteus syndrome.
  Lindhurst, M.J., Wang, J., Bloomhardt, H., Wikowski, A.M., Singh, L.N., Bick, D.P., Gambello, M.J., Powell, C.M., Darling, T.N., Lee, C. R., Biesecker, L.G., American Society of Human Genetics Annual Meeting, Boston, MA, 1/22/2013
• A Simplified Method for Screening Siblings for HLA Identity Using Short Tandem Repeat (STR) Polymorphisms.
  Schiller, J.J., Hopp, K.A., Pietz, B.C., Bick, D.P., Lau, E.C., Ellis, T.M., Hum Immunol, 1/3/2013
• Advances in PGD.
  Lau, E., Janson, M., Ball, C., Roesler, M., Strawn, E., Bick, D.P., BIT Life Sciences 2nd World DNA and Genome Day-2011 Congress, Dalian, China, 1/25/2011
• Next Generation Sequencing-Standardization of clinical testing (NEX-StoCT): Approaches to quality assurance and complying with regulatory and professional standards.
  Gargis, A.S., Kalman, L.V., Berry, M., Bick, D.P., Dimmock, D.P., Hambauch, T.M., Lu, F., Lyon, E., Voelkerding, K.V., Zehnbauer, B.A., Lubin, L.M., and Working Group, Association for Molecular Pathology's 2011 Annual Meeting, Grapevine, TX, 1/17/2011
• Experience with the analysis and management of data from whole genome sequencing in clinical practice.
  Taylor, B., Jacob, H., Schauer, D., North, P., Sander, T., McQuestion, G., BICK, D., Dimmock, D., American College of Medical Genetics Annual Meeting, Vancouver, Canada, 1/1/2011
• Clinical Whole Genome Sequencing: One Center's Experience.
  Dimmock, D., Willoughby Jr., R., Leuthner, S., Veith, R., Gutzeit, M., May, T., Hambuch, T., Worthey, E., Jacob, H., Tschannen, M., North, P., BICK, D., American College of Medical Genetics Annual Meeting, Vancouver, Canada, 1/1/2011
• Clinical Whole Genome Sequencing: Genetic Counseling and Informed Consent for Anticipated Incidental Findings Collection.
  Veith, R., Dimmock, D., BICK, D., White, A., Dugan, S., American College of Medical Genetics Annual Meeting, Vancouver, Canada, 1/1/2011
• 11p15.4p15.5 Duplication Associated with Russell-Silver Syndrome.
  Sekhri, N., VanTuinen, P., Broeckel, U., Bick, D.P., American College of Medical Genetics Annual Meeting, Albuquerque, NM, 1/24/2010
• Clinical Utility of Whole Exome Sequencing in the Diagnosis of a Child.
  Dimmock, D., Worthy, E., Mayer, A., Verbsky, J., Bick, D.P., Routes, J., Schannen, M., Helbling, D., Schauer, D., Veith, R., Jacob, H., American College of Medical Genetics Annual Meeting, Albuquerque, NM, 1/1/2010
• Revealing the mystery behind 'The Elephant Man': Proteomic characterization of Proteus Syndrome.
  Mirza, S.P., Duffy, K., Chesnik, M.A., Cole, R., Bick, D.P., Olivier, M., 57th ASMS Conference on Mass Spectrometry, Philadelphia, PA, 1/31/2009
• Immune Modulation Therapy in a CRIM Negative Pompe Disease Patient Blocks Antibody Formation Towards Myozyme, Reverses Cardiomyopathy, and Prolongs Survival.
  Rhead, W.R., Wells, C., Bick, D.P., Margolis, D., Kishnani, P., Bali, D., Young, S., White, A., International Congress of Inborn Errors of Metabolism, San Diego, CA, 1/29/2009
• 18q12.1 Interstitial microduplication in mother and child: A case report.
  Veith, R., Swanson, A., Denny, A., Leuthner, S., Mitchell, A., BICK, D. P., American Society of Human Genetics Annual Meeting, Philadelphia, PA, 1/11/2008
• Microdeletion at 9q33.3q34.11 encompassing the LMX1B and ENG genes: A case report.
  Trapane, P., Jarzembowski, J., Bick, D.P., Rhead, W., Wargowski, D., Aradhya, S., Mitchell, A., Veith, R., American Society of Human Genetics Annual Meeting, Philadelphia, PA, 1/11/2008
• Somatic partial chromosome 11 duplication in patients with Proteus Syndrome.
  Duffy, K., Bick, D.P., vanTuinen, P., Dugan, S., Yilmaz, A., Schwartz, C., Foulkes, W., Olivier, M., ASHG Annual Meeting, San Diego, CA, 1/1/2007
• Development of a rapid protocol for molecular diagnosis of spinal muscular atrophy in preimplantation genetic diagnosis by whole genome amplification and pyrosequencing.
  Schneider, R.J., Lau, E., Schur, B., Wong, S., Bick, D.P., Clin Chem, 1/1/2007
• Somatic partial chromosome 11 duplication in a patient with Proteus Syndrome.
  Duffy, K., Bick, D.P., vanTuinen, P., Dugan, S., Olivier, M., ACMG 13th Annual Meeting, Nashville, TN, 1/1/2007
• Interstitial deletion of chromosome 12q: Genotype-phenotype correlation of 2 patients utilizing array comparative genomic hybridization.
  Klein, O.D, Cotter, P.D., Weiss, A., Bick, D.P., Albertson, D.G., Pinkel, D., Rauen, K.A., ACMG, 10th Annual Meeting, Kissimmee, FL, 1/1/2004
• Prevalence of gonadotropin-releasing hormone receptor mutations in humans with idiopathic hypogonadotropic hypogonadism.
  Bhagavath, B., Ozata, M., Golu, E., Ozdemir, I.C., Bick, D.P., Sherins, R, Layman, LC, Endocrine Society Meeting, 85th Annual Meeting, 1/1/2003
• Molecular characterization of a patient with oculo-auriculo-vertebral spectrum.
  Joseph, N., Bick, D.P., Howard-Peebles, P.N., Overhauser, J., Marinescu, R. C., Li, M.M., Am J Hum Genet, 1/1/1998
• Ethylmalonic aciduria in short-chain acyl CoA dehydrogenase deficiency: Recognition of the phenotype, genetic polymorphism and clinical implications.
  Lavenstein, B., Bick, D.P., Rinaldo, P., Ann of Neuro, 1/1/1997
• The low frequency of Kallmann syndrome (KAL) gene mutations in humans with hypogonadotropic hypogonadism suggests non-X linked modes of inheritance.
  Layman, L.C., Kalimullah, E., Boachie-Ansah, G., Xie, J., Jin, M., Amde, S., Shah, S. Kawada, P., Pampoonsup, W., Sherins, R.J., Bick, D.P., Society of Gynecologic Investigation, 1/1/1997
• Association of prenatally diagnosed confined placental mosaicism (CPM) and fetal gonadal mosaicism.
  Stavropoulos, D.J., Barrett, I.J., Lomax, B.L., Bick, D.P., Bernasconi, F., Robinson, W.P., Kalousek, D.K., Am J Hum Genet, 1/1/1997
• Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLO) in a sex-reversed fetus.
  Bick, D.P., Stanley, W.S., Stern, H.J., Berkovitz, G.D., Meyers, C.M., Kelley, R.I., Am J Hum Genet, 1/1/1997
• Contribution of the molecular genetics laboratory to the evaluation of the persistently hypotonic infant.
  Spence, W.C., Maddalena, A., Howard-Peebles, P.N., Bick, D.P., Am Ped Society and Society Pediatr Research, 1/1/1996
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Lectures

• Genetic Testing in the Era of Next Generation Sequencing 
  West Allis, WI - 1/27/2015
• Overview of NGS: A Comparison of WGS/WES Versus Microarray Testing in the Evaluation of Intellectual Disability, Autism and/or Multiple Congenital Anomalies 
  Salt Lake City, UT - 1/25/2015
• When to Order an Exome (Versus Other Genetic Tests) and Variant Interpretation in the Context of WES vs. Single Genes and Panels 
  Salt Lake City, UT - 1/24/2015
• Developing a Clinical and Laboratory Genomic Medicine Program 
  Nationwide Children's Hospital, Columbus, OH - 1/31/2014
• How should physicians integrate the new variant classification guidelines into clinica care? 
  Nashville, TN - 1/25/2014
• Genetics 101: Fundamental Principles and Prenatal Genetics for the Pediatrician 
  Medical College of Wisconsin, Milwaukee, WI - 1/20/2014
• Using Genomic Sequencing in Clinical Practice Today 
  Children's Hospital of Wisconsin, Milwaukee, WI - 1/12/2014
• Genomic Sequencing in Clinical Practice 
  Milwaukee, WI - 1/2/2014
• Whole Genome Sequencing in Children: Ready for Prime Time? 
  Orlando, FL - 1/26/2013
• Medical College of Wisconsin Experience: Reimbursement Successes and Failures "In House" WES/WGS 
  Phoenix, AZ - 1/23/2013
• Challenges and Accomplishments of Exome and Genome Sequencing 
  Phoenix, AZ - 1/23/2013
• MCW/CHW clinical and laboratory genomic medicine program - a progress report. 
  Medical College of Wisconsin, Milwaukee, WI - 1/18/2013
• Infantile Myofribromatosis 
  Milwaukee, WI - 1/17/2013
• Kabuki Syndrome and Histone deacetylase inhibitors. 
  Mukwonago, WI - 1/13/2013
• Genetic Testing in 2013 
  Milwaukee, WI - 1/13/2013
• Genome Sequencing in Clinical Practice 
  Medical College of Wisconsin, Milwaukee, WI - 1/11/2013
• Developing a clinical and laboratory genomic medicine program. 
  Cincinnati Children's Medical Center, Cincinnati, OH - 1/9/2013
• Genetic Testing 2013 and Beyond, Best Practices in Pediatrics 
  Wisconsin Dells, WI - 1/9/2013
• Whole Genome and Whole Exome Sequencing in the Clinic 
  Long Beach, CA - 1/26/2012
• Whole Genome Sequencing in Clinical Practice Today 
  Duke University Health Systems, Durham, NC - 1/17/2012
• Current State of Practice: Whole Genome Sequencing in Clinical Use Today 
  Milwaukee, WI - 1/17/2012
• Whole Genome Sequencing in Clinical Practice 
  Atlanta, GA - 1/12/2012
• Informatics in Next - Generation Sequencing: NGS Will Change the Practice of Medicine 
  Atlanta, GA - 1/11/2012
• Online Resources for Genetics 
  Medical College of Wisconsin, Milwaukee, WI - 1/10/2012
• Genetic Screening : What Should I Offer to My Patients? 
  Milwaukee, WI - 1/4/2012
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