Steve Scherer

发表

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)

Todd E. Scheetz, Adam P. DeLuca, A. Eliot Shearer, 2011, Proceedings of the National Academy of Sciences.

Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

C. Marshall, P. Sham, You-Qiang Song, 2012, PLoS genetics.

MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II.

D. Milewicz, D. Guo, A. Marian, 2007, Human molecular genetics.

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (vol 39, pg 1488, 2007)

Robert K. Yu, S. Shete, D. Milewicz, 2008 .

Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Robert K. Yu, S. Shete, D. Milewicz, 2007, Nature Genetics.

Corrigendum: Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Robert K. Yu, S. Shete, D. Milewicz, 2008, Nature Genetics.

MYH 11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II

D. Milewicz, D. Guo, A. Marian, 2007 .

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing

Adam P. DeLuca, T. Scheetz, Richard J. H. Smith, 2010, Proceedings of the National Academy of Sciences.

Using the Phenome and Genome to Improve Genetic Diagnosis for Deafness

Adam P. DeLuca, T. Casavant, T. Scheetz, 2012, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Correction: Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

C. Marshall, P. Sham, You-Qiang Song, 2012, PLoS Genetics.

The genomic, evolutionary and functional landscapes of anaplastic thyroid carcinoma

John D. Watson, Cipriani, P. Boutros, 2023, medRxiv.

Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Timothy B Sackton, Jay D. Evans, Jay D Evans, 2007, Nature Genetics.

Erratum: MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor1 and angiotensin II (Human Molecular Genetics (2007) vol. 16 (20) (2453-2462) 10.1093/hmg/ddm201)

D. Milewicz, A. Marian, A. Brasier, 2008 .

O2Targeted-genomic capture and high-throughput sequencing for genetic testing and new gene discovery in atypical hemolytic uremic syndrome

Adam P. DeLuca, T. Scheetz, Richard J. H. Smith, 2011 .