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Anne V. Hing, MD

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Anne V. Hing, MD

Craniofacial, Genetics, Pediatrics-Inpatient, Vascular Anomalies

On staff since March 2000

Academic Title: Associate Professor

Research Center: Center for Developmental Biology and Regenerative Medicine

Recommendations

KristaUniversity Place, Washington01.12.12
It is never easy learning your child has a genetic disorder and that there is not much information available about the disorder. Dr. Hing is a knowledgable and caring doctor who has explained OFD to me, always provides me with up to date reseach and most importantly take amazing care of my daugher.
Recommend Dr. Anne Hing

Overview

Board Certification(s)
Clinical Genetics (MD)
Pediatrics
Medical/Professional School
Washington University School of Medicine, St Louis
Residency
Pediatrics, St Louis Children's Hospital, St Louis
Fellowship
Medical Genetics, Washington University School of Medicine, St Louis
Lab URL

http://www.seattlechildrens.org/research/developmental-biology-regenerative-medicine/hing-studies/

Research Focus Area

Craniofacial

Awards and Honors

Award NameAward DescriptionAwarded ByAward Date
Richard A. Molteni AwardSeattle Children's Hospital 2012
Poncin Foundation Scholarship 2001
Edward Mallinckrodt Jr. Foundation Scholarship 1995
Alpha Omega Alpha, Medical Honor Society 1985
George F. Gill Prize in Pediatrics 1985
Dr. Margaret G. Smith Award for Outstanding Achievement by a Woman Medical Student in the First Two Years of Medical School, Scholarship Achievement CitationAmerican Medical Woman's Association, Inc. 1983
Edmund V. Cowdry Prize in Histology 1982
Kappa Alpha Pi-Scholastic Honor Society 1981

Publications

Making the diagnosis: metopic ridge versus metopic craniosynostosis.
The Journal of craniofacial surgery , 2013 Jan: 24(1)178-85
"Mandibulofacial dysostosis with microcephaly" caused by EFTUD2 mutations: expanding the phenotype.
American journal of medical genetics. Part A , 2013 Jan: 161A(1)108-13
Bathrocephaly: a head shape associated with a persistent mendosal suture.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association , 2013 Jan: 50(1)104-8
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
American journal of human genetics , 2012 May 4: 90(5)907-14
New developments in genetic diagnosis: implications for the craniofacial surgeon.
The Journal of craniofacial surgery , 2012 Jan: 23(1)212-6
IGF1R variants associated with isolated single suture craniosynostosis.
American journal of medical genetics. Part A , 2011 Jan: 155A(1)91-7
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.
American journal of medical genetics. Part A , 2010 Sep: 2203-10
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.
Genetics in medicine : official journal of the American College of Medical Genetics , 2010 Aug 30
Picture perfect? Reliability of craniofacial anthropometry using three-dimensional digital stereophotogrammetry.
Plastic and reconstructive surgery , 2009 Oct: 1261-72
Bilateral lambdoid and sagittal synostosis (BLSS): a unique craniosynostosis syndrome or predictable craniofacial phenotype?
American journal of medical genetics. Part A , 2009 May: 1024-32
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.
American journal of human genetics , 2009 Mar: 84(3)406-11
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
Nature genetics , 2009 Jan: 95-100
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization.
Molecular Cytogenetics , 2008 Apr 21: 7
The morphogenesis of wormian bones: a study of craniosynostosis and purposeful cranial deformation.
American journal of medical genetics. Part A , 2007 Dec 15: 3243-51
Syndromic craniosynostosis: from history to hydrogen bonds.
Orthodontics & craniofacial research , 2007 May: 67-81
Sleep disturbances in 22q11.2 deletion syndrome: a case with obstructive and central sleep apnea.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association , 2007 May: 340-6
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.
American journal of medical genetics. Part A , 2007 Apr 1: 678-86
A novel oculo-oto-facial dysplasia in a Native Alaskan community with autosomal recessive inheritance.
American journal of medical genetics. Part A , 2006 Apr 15: 804-12
New scaphocephaly severity indices of sagittal craniosynostosis: a comparative study with cranial index quantifications.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association , 2006 Mar: 211-21
Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.
Birth defects research. Part A, Clinical and molecular teratology , 2006 Feb: 78-85
MDCT diagnosis of the child with posterior plagiocephaly.
AJR. American journal of roentgenology , 2005 Nov: 1342-6
Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance.
American journal of medical genetics. Part A , 2004 Aug 1: 374-82

Research Funding

Grant TitleGrantorAmountAward Date
Genetic and Developmental Pathways Causing Midfacial HypoplasiaNIH NIDCR $, $2,278,095 2012 - 2017

Primary Office

Seattle Children's
OB.9.520 - Craniofacial
4800 Sand Point Way NE
Seattle, WA 98105
206-987-2208

Additional Offices

Seattle Children's
OC.9.850 - Medical Genetics
4800 Sand Point Way NE
Seattle, WA 98105
206-987-2056

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