Steven A Wall Selected Research

Synostosis

1/2022	Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders.
1/2019	ERF-related craniosynostosis: The phenotypic and developmental profile of a new craniosynostosis syndrome.
1/2016	Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis.
12/2015	Association of mutations in FLNA with craniosynostosis.
3/2013	Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.
3/2013	Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
6/2009	Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
7/2008	Implications of a vertex bulge following modified strip craniectomy for sagittal synostosis.
4/2006	Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!

Steven A Wall Research Topics

Disease

17	Craniosynostoses (Craniosynostosis) 01/2022 - 02/2002
9	Synostosis 01/2022 - 04/2006
3	Acrocephalosyndactylia (Apert Syndrome) 10/2018 - 04/2005
3	Craniofrontonasal dysplasia 04/2013 - 06/2004
2	Language Development Disorders (Semantic-Pragmatic Disorder) 01/2019 - 03/2013
2	Hypertelorism 04/2013 - 06/2004
2	Muenke Syndrome 01/2009 - 08/2004
1	Eczema 09/2017
1	Reinfection 09/2017
1	Acute-Phase Reaction 09/2017
1	Bronchiectasis 09/2017
1	Eosinophilia 09/2017
1	Congenital Abnormalities (Deformity) 06/2017
1	Periventricular Nodular Heterotopia 12/2015
1	Learning Disabilities (Learning Disability) 09/2015
1	Pneumocephalus 12/2013
1	Ter Haar syndrome 11/2012
1	Supernumerary Tooth (Supernumerary Teeth) 07/2011
1	Chromosome Aberrations (Chromosome Abnormalities) 06/2010
1	Hearing Loss (Hearing Impairment) 01/2009
1	Sensorineural Hearing Loss 01/2009
1	Hydrocephalus (Hydrocephaly) 07/2008
1	Neural Tube Defects (Exencephaly) 06/2007
1	Developmental Bone Diseases (Bone Dysplasia) 02/2002

Drug/Important Bio-Agent (IBA)

6	Ephrin-B1 (Ephrin B1)IBA 01/2017 - 06/2004
2	Proteins (Proteins, Gene)FDA Link 12/2015 - 02/2002
2	Type 2 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 2)IBA 08/2014 - 02/2002
2	Type 3 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 3)IBA 01/2009 - 05/2005
2	LigandsIBA 01/2009 - 04/2005
2	EphrinsIBA 04/2006 - 06/2004
2	Fibroblast Growth Factor Receptors (Fibroblast Growth Factor Receptor)IBA 04/2005 - 08/2004
1	RNA (Ribonucleic Acid)IBA 01/2022
1	Transcription Factors (Transcription Factor)IBA 01/2019
1	factor AIBA 01/2019
1	5' Untranslated Regions (5' UTR)IBA 10/2018
1	Immunoglobulin E (IgE)IBA 09/2017
1	Complementary DNA (cDNA)IBA 01/2016
1	DNA (Deoxyribonucleic Acid)IBA 01/2016
1	FilaminsIBA 12/2015
1	Basic Helix-Loop-Helix Transcription FactorsIBA 03/2013
1	Interleukin-11 (Interleukin 11)IBA 07/2011
1	Genetic Markers (Genetic Marker)IBA 06/2010
1	Nonsense Codon (Nonsense Mutation)IBA 06/2007
1	Ephrin-A4 (Ephrin A4)IBA 04/2006
1	Protein Isoforms (Isoforms)IBA 04/2005
1	NucleotidesIBA 08/2004
1	EphA1 Receptor (Eph Receptor)IBA 06/2004

Therapy/Procedure

11	Sutures (Suture) 01/2022 - 02/2002
1	Operative Surgical Procedures 06/2017
1	Free Tissue Flaps 12/2013
1	Therapeutics 01/2009
1	Ventriculoperitoneal Shunt 07/2008
1	Craniotomy 07/2008