DavidPBickMD

PubMed

• 10 citations
  PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum
  Katrine M Johannesen, Elena Gardella, Cathrine E. Gjerulfsen, Allan Bayat, Rob P.W. Rouhl, Margot R.F. Reijnders, Sandra Whalen, Boris Keren, Julien Buratti, Thomas Co...> ;Neurology. Genetics. 2021 Nov 15
• 6 citations
  A study of elective genome sequencing and pharmacogenetic testing in an unselected population
  Meagan Cochran, Kelly M. East, Veronica Greve, Melissa Kelly, Whitley V. Kelley, Troy Moore, Richard M. Myers, Katherine Odom, Molly C Schroeder, David Bick> ;Molecular Genetics & Genomic Medicine. 2021 Jul 27
• 6 citations
  One is the loneliest number: genotypic matchmaking using the electronic health record.
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;Genetics in Medicine. 2021 Jul 6
• 52 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, Soma Das, Julianne M. O’Daniel, Heidi L. Rehm, Vandana Shashi, Lisa M. Vincent> ;Genetics in Medicine. 2021 Apr 29
• 6 citations
  Reducing Sanger confirmation testing through false positive prediction algorithms.
  James Holt, Melissa A. Kelly, Brett Sundlof, Ghunwa Nakouzi, David P. Bick, Elaine Lyon> ;Genetics in Medicine. 2021 Mar 25
• 18 citations
  Functional and structural analysis of cytokine selective IL6ST defects that cause recessive hyper-IgE syndrome
  Yin-Huai Chen, Diane B. Zastrow, Riley D. Metcalfe, Lisa Gartner, Freia Krause, Craig J. Morton, Shruti Marwaha, Laure Fresard, Yong Huang, Chunli Zhao, Colleen E. McC...> ;The Journal of Allergy and Clinical Immunology. 2021 Mar 23
• 21 citations
  An online compendium of treatable genetic disorders.
  David P. Bick, Sarah L Bick, David Dimmock, Tom Fowler, Mark J. Caulfield, Richard H Scott> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2021 Mar 1
• 32 citations
  Clinical utility of genomic sequencing: a measurement toolkit
  Robin Z. Hayeems, David Dimmock, David P. Bick, John W Belmont, Robert C. Green, Brendan C. Lanpher, Vaidehi Jobanputra, Roberto Mendoza, Shashi Kulkarni, Megan E. Gro...> ;NPJ Genomic Medicine. 2020 Dec 15
• 51 citations
  Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease
  Christian R. Marshall, Shimul Chowdhury, Ryan J. Taft, Mathew S Lebo, Jillian G. Buchan, Steven M. Harrison, Ross A. Rowsey, Eric W. Klee, Pengfei Liu, Elizabeth A. Wo...> ;NPJ Genomic Medicine. 2020 Oct 23
• 32 citations
  The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic.
  Christian R. Marshall, David P. Bick, John W Belmont, Stacie L Taylor, Euan A. Ashley, David Dimmock, Vaidehi Jobanputra, Hutton M. Kearney, Shashikant Kulkarni, Heidi...> ;Genome Medicine. 2020 May 27
• 13 citations
  Design and Reporting Considerations for Genetic Screening Tests
  Jill M. Hagenkord, Birgit Funke, Emily Qian, Madhuri Hegde, Kevin B. Jacobs, Matthew J. Ferber, Matthew S. Lebo, Adam H. Buchanan, David P. Bick> ;The Journal of Molecular Diagnostics. 2020 May 1
• 7 citations
  Expanding the phenotype of the CDKL5 deficiency disorder: Are seizures mandatory?
  Conor I. MacKay, David P. Bick, Jeremy W. Prokop, Ivan Muñoz, John Rouse, Jenny Downs, Helen Leonard> ;American Journal of Medical Genetics. Part A. 2020 Feb 8
• 35 citations
  Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;Biological Psychiatry. 2020 Jan 15
• 8 citations
  Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The A...
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;American Journal of Human Genetics. 2019 Sep 5
• 47 citations
  Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification.
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;American Journal of Human Genetics. 2019 Jun 6
• 56 citations
  De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypes
  Lina Liang, Xia Li, Sebastien Moutton, Samantha A. Schrier Vergano, Benjamin Cogné, Anne de Saint-Martin, Anna C.E. Hurst, Y. T. Hu, Olaf Bodamer, Julien Thevenon, Chr...> ;Human Molecular Genetics. 2019 Sep 1
• 63 citations
  Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
  David P. Bick, Marilyn C. Jones, Stacie L Taylor, Ryan J. Taft, John W Belmont> ;Journal of Medical Genetics. 2019 Apr 25
• 8 citations
  A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing
  Diane B. Zastrow, Jennefer N. Kohler, Devon Bonner, Chloe M. Reuter, Liliana Fernandez, Megan E. Grove, Dianna G. Fisk, Yaping Yang, Christine M. Eng, Patricia A. Ward...> ;Journal of Genetic Counseling. 2019 Apr 1
• 8 citations
  Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients.
  Kelly M. East, Meagan Cochran, Whitley V. Kelley, Veronica Greve, Kristina Emmerson, Grace Raines, Jesse Nicholas Cochran, Adam M. Hott, David P. Bick> ;Journal of Genetic Counseling. 2019 Apr 1
• 50 citations
  Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay
  Keren Machol, Justine Rousseau, Sophie Ehresmann, Thomas Garcia, Thi Tuyet Mai Nguyen, Rebecca C. Spillmann, Jennifer A. Sullivan, Vandana Shashi, Yong-hui Jiang, Nich...> ;American Journal of Human Genetics. 2019 Jan 3
• 16 citations
  Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic Testing.
  James T. Lu, Matthew J. Ferber, Jill M. Hagenkord, Elissa Levin, Sarah T. South, Hyunseok Kang, Kimberly A. Strong, David P. Bick> ;The Journal of Molecular Diagnostics. 2019 Jan 1
• 46 citations
  Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
  Ning Liu, Kelly Schoch, Xi Luo, Loren D M Pena, Venkata Hemanjani Bhavana, Mary K. Kukolich, Sarah Stringer, Zöe Powis, Kelly Radtke, Cameron Mroske, Kristen L. Deak, ...> ;Human Molecular Genetics. 2018 Jul 15
• 7 citations
  Response to Biesecker and Harrison.
  C. Sue Richards, Nazneen Aziz, Sherri J. Bale, David P. Bick, Soma Das, Julie M. Gastier-Foster, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Elaine B. Spector, Karl V....> ;Genetics in Medicine. 2018 Dec 1
• 4 citations
  A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33).
  Jess F. Peterson, Donald Basel, David P. Bick, Brett Chirempes, Rachel B. Lorier, Nykula Zemlicka, John W. Grignon, LuAnn Weik, Ulrike P. Kappes> ;Journal of Pediatric Genetics. 2017 Jul 26
• 53 citations
  Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,...> ;American Journal of Human Genetics. 2018 Mar 1
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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
• 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
• Ehtical issues in DNA sequencing in the neonate  
  Dimmock, D.P., Bick, D.P., Clin Perinatol, 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• Preimplantation Genetic Diagnosis: Technology and Clinical Applications  
  Swanson, A., Strawn, E., Lau, E., BICK, D., Wis Med J, 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
• DNA-based X-enriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease  
  Levinson, G., Keyvanfar, K., Wu, J.C., Fugger, E.F., Fields, R.A., Harton, G.L., Palmer, F.T., Sisson, M.E., Starr, K.M., Dennison-Lagos, L., Calvo, L., Sherins, R.J.,..., Human Mol Reprod, 1/1/1995
• DNA-based prenatal determination of the RhE genotype  
  Spence, W.C., Potter, P., Maddalena, A., Demers, D.B. Bick, D.P., Obstet Gynecol, 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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
• 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 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
• 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
• 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
• 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
• 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
• 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
• 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
• Challenges and Accomplishments of Exome and Genome Sequencing 
  Phoenix, AZ - 1/23/2013
• Medical College of Wisconsin Experience: Reimbursement Successes and Failures "In House" WES/WGS 
  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
• Genetic Testing in 2013 
  Milwaukee, WI - 1/13/2013
• Kabuki Syndrome and Histone deacetylase inhibitors. 
  Mukwonago, WI - 1/13/2013
• Genome Sequencing in Clinical Practice 
  Medical College of Wisconsin, Milwaukee, WI - 1/11/2013
• Genetic Testing 2013 and Beyond, Best Practices in Pediatrics 
  Wisconsin Dells, WI - 1/9/2013
• Developing a clinical and laboratory genomic medicine program. 
  Cincinnati Children's Medical Center, Cincinnati, OH - 1/9/2013
• Whole Genome and Whole Exome Sequencing in the Clinic 
  Long Beach, CA - 1/26/2012
• Current State of Practice: Whole Genome Sequencing in Clinical Use Today 
  Milwaukee, WI - 1/17/2012
• Whole Genome Sequencing in Clinical Practice Today 
  Duke University Health Systems, Durham, NC - 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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