Stephen T Warren

发表

PEMapper / PECaller: A simplified approach to whole-genome sequencing

Jennifer Mulle, Michael E Zwick, Michael P Epstein, 2016, bioRxiv.

Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes

Michael E Zwick, Pankaj Chopra, Michael P Epstein, 2017, Proceedings of the National Academy of Sciences.

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

Stephen T Warren, Somayyeh Fahiminiya, E. Zackai, 2012, Journal of Medical Genetics.

Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum.

Tao Wang, Peng Jin, Qian Pan, 2012, Human molecular genetics.

Genome‐wide association study of schizophrenia in Ashkenazi Jews

Vladimir Vacic, Ingo Ruczinski, Mehdi Pirooznia, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Urvashi Surti, Swaroop Aradhya, Margaret P Adam, 2010, American journal of human genetics.

Fragile X Syndrome: An Update and Review for the Primary Pediatrician

Stephen T Warren, S. Warren, J. Graham, 2005, Clinical pediatrics.

Physiological identification of human transcripts translationally regulated by a specific microRNA.

Peng Jin, Stephen T Warren, P. Jin, 2005, Human molecular genetics.

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

Swaroop Aradhya, Michael R Rossi, Vineith Kaul, 2011, Genetics in Medicine.

Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundaries.

Stephen T Warren, 2003, American journal of human genetics.

A decade of molecular studies of fragile X syndrome.

Stephen T Warren, S. Warren, William T O'Donnell, 2002, Annual review of neuroscience.

Fragile X syndrome

Stephen T Warren, S. Warren, Kathryn B Garber, 2008, European Journal of Human Genetics.

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.

Stephen T Warren, Christa L Martin, S. Spence, 2007, Human molecular genetics.

Molecular mechanisms of fragile X syndrome: a twenty-year perspective.

Stephen T Warren, S. Warren, S. Bray, 2012, Annual review of pathology.

Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences.

Pankaj Chopra, Stephen T Warren, S. Warren, 2014, Human molecular genetics.

The mGluR theory of fragile X mental retardation

Mark F Bear, Stephen T Warren, M. Bear, 2004, Trends in Neurosciences.

Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors

Stephen T Warren, Usha Narayanan, Mika Nakamoto, 2007, Proceedings of the National Academy of Sciences.