HollyHutchisonArdingerMD

Medical Genetics • Bainbridge Island, WA

Clinical Genetics

Associate Professor of Pediatrics, University MO-Kansas City

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Office
12404 Kallgren Rd NE
Bainbridge Island, WA 98110
Phone+1 913-523-5626
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Summary

Dr. Holly Ardinger, MD is a board certified medical geneticist in Bainbridge Island, Washington. She is currently licensed to practice medicine in Washington, Missouri, and Kansas. She is an Associate Professor of Pediatrics at University MO-Kansas City.

Education & Training

University of Iowa Hospitals and ClinicsPediatrics/Medical Genetics, 1985 - 1989
University of Iowa Hospitals and ClinicsResidency, Pediatrics, 1983 - 1985
University of California (San Diego) Medical CenterResidency, Pediatrics, 1981 - 1983
University of Iowa Roy J. and Lucille A. Carver College of MedicineClass of 1981

Certifications & Licensure

WA State Medical License 2016 - 2019
KS State Medical License 1990 - 2017
MO State Medical License 1995 - 2017
American Board of Medical Genetics and Genomics Clinical Genetics
American Board of Pediatrics Pediatrics

Awards, Honors, & Recognition

Regional Top Doctor Castle Connolly, 2014
Fellow (FAAP) American Academy of Pediatrics

Publications & Presentations

PubMed

9 citations
Family history and clefting as major criteria for CHARGE syndrome.
Susan Starling Hughes, Holly I Welsh, Nicole P. Safina, Khemissa Bejaoui, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2014 Jan 1
13 citations
Aggressive juvenile polyposis in children with chromosome 10q23 deletion.
Seth Septer, Lei Zhang, Caitlin E. Lawson, Jose Cocjin, Thomas M. Attard, Holly H Ardinger> ;World Journal of Gastroenterology. 2013 Apr 14
59 citations
Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog
Benjamin D. Solomon, Kelly A. Bear, Adrian Wyllie, Amelia A. Keaton, Christèle Dubourg, Véronique David, Sandra Mercier, Sylvie Odent, Ute Hehr, Aimee D C Paulussen, N...> ;Journal of Medical Genetics. 2012 Jul 1
3 citations
CDKN1C mutations and genital anomalies
Holly I Welsh, Tracy Stockley, Nicole Parkinson, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2012 Jan 1
1 citations
Total absence of ribs in a newborn with cerebrocostomandibular syndrome.
Seema Lale, Holly H. Ardinger, Neil J. Mardis, Sheelah Changho, Thomas Lancaster, Vivekanand Singh> ;Pediatric and Developmental Pathology. 2011 Mar 1
8 citations
Petty syndrome and Fontaine-Farriaux syndrome: Delineation of a single syndrome.
Stephen R. Braddock, Holly H. Ardinger, Chun-Song Yang, Bryce M. Paschal, Bryan D. Hall> ;American Journal of Medical Genetics. Part A. 2010 Jul 1
27 citations
Comprehensive ZEB2 gene analysis for Mowat-Wilson syndrome in a North American cohort: a suggested approach to molecular diagnostics.
Carol J Saunders, Weiwei Zhao, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2009 Nov 1
19 citations
A child with terminal 14q deletion syndrome: Consideration of genotype–phenotype correlations
Kamilla Schlade-Bartusiak, Holly H. Ardinger, Diane W. Cox> ;American Journal of Medical Genetics. Part A. 2009 May 1
2 citations
The Hunter-MacDonald syndrome with expanded phenotype including risk of meningioma: an update and review.
Linlea Armstrong, Gail E. Graham, R. Neil Schimke, Debra L. Collins, Daniel J. Kirse, Fiona Costello, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2008 Jan 1
27 citations
Expanding the phenotype of oculoectodermal syndrome: possible relationship to encephalocraniocutaneous lipomatosis.
Holly H. Ardinger, Kimberly A. Horii, Michael L. Begleiter> ;American Journal of Medical Genetics. Part A. 2007 Dec 15
1 citations
Maternal serum screening and 22q11.2 deletion syndrome
Michael L. Begleiter, Molly M. Lund, Andrea M. Atherton, Janda D. Buchholz, Holly H. Ardinger> ;American Journal of Medical Genetics. Part A. 2007 Feb 15
Classification of cardiovascular malformations associated with neuroblastoma.
Angela E. Lin, Holly H. Ardinger, Mary Ella M Pierpont, Rani E. George, Lisa Diller, Steven E. Lipshultz, Stuart R. Lipsitz, Steven D. Colan, Edward B. Clark> ;The Journal of Pediatrics. 2005 Mar 1
157 citations
Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.
Inessa Grinberg, Hope Northrup, Holly H. Ardinger, Chitra Prasad, William B. Dobyns, Kathleen J. Millen> ;Nature Genetics. 2004 Aug 29
610 citations
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
Shinji Kondo, Brian C. Schutte, Rebecca J. Richardson, Bryan C. Bjork, Alexandra S. Knight, Yoriko Watanabe, Emma Howard, Renata Lúcia Leite Ferreira de Lima, Sandra D...> ;Nature Genetics. 2002 Oct 1
53 citations
Cardiovascular malformations in Smith-Lemli-Opitz syndrome
Angela E. Lin, Holly H. Ardinger, Robert H. Ardinger, Christopher Cunniff, Richard I. Kelley> ;American Journal of Medical Genetics. 1997 Jan 31
67 citations
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).
Rita Shiang, Andrew C. Lidral, H H Ardinger, Kenneth H. Buetow, Paul A. Romitti, Ronald G. Munger, Jeffrey C. Murray> ;American Journal of Human Genetics. 1993 Oct 1
78 citations
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.
Jeffrey C. Murray, Darryl Y. Nishimura, Kenneth H. Buetow, H H Ardinger, M. A. Spence, R. S. Sparkes, R. E. Falk, P. M. Falk, R. J. M. Gardner, E. M. Harkness, L. P. G...> ;American Journal of Human Genetics. 1990 Mar 1
229 citations
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate.
H H Ardinger, Kenneth H. Buetow, Graeme I. Bell, Janusz Bardach, D R VanDemark, Jeffrey C. Murray> ;American Journal of Human Genetics. 1989 Sep 1
10 citations
RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.
H.H. Ardinger, Robert H Ardinger, Graeme I. Bell, Jeffrey C. Murray> ;Nucleic Acids Research. 1988 Aug 25
208 citations
Verification of the fetal valproate syndrome phenotype.
Holly H Ardinger, Joan F. Atkin, R D Blackston, Louis J. Elsas, Sterling K. Clarren, S Livingstone, D B Flannery, J M Pellock, Mary Jo E. Harrod, Edward J. Lammer> ;American Journal of Medical Genetics. 1988 Jan 1
11 citations
Dominantly inherited dilated cardiomyopathy.
R. J. M. Gardner, James W. Hanson, Victor Ionasescu, H. H. Ardinger, David J. Skorton, Larry T. Mahoney, M. N. Hart, E. F. Rose, Wilbur L. Smith, M. S. Florentine> ;American Journal of Medical Genetics. 1987 May 1
5 citations
Association of neural tube defects with omphalocele in chromosomally normal fetuses.
H. H. Ardinger, Roger A. Williamson, Grant S> ;American Journal of Medical Genetics. 1987 May 1
37 citations
Further delineation of Weaver syndrome
Holly H. Ardinger, James W. Hanson, Mary Jo E. Harrod, M. Michael Cohen, John A.R. Tibbles, J. Philip Welch, Theresa Young-Wee, Annemarie Sommer, Rosalie Goldberg, Rob...> ;The Journal of Pediatrics. 1986 Feb 1
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Professional Memberships

American Academy of Pediatrics - AAP
Fellow