author-photo

Margaret N. Berry

Wake Forest University

20

Papers

466

Citations

Citation Trend

Filter By

Papers (13) Sort By

Journal Conference Others

The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.

2015 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (24)
De novo Mutations in NALCN Cause a Syndrome of Congenital Contractures of the Limbs and Face with Hypotonia, and Developmental Delay

2015 bioRxiv
Show All
- Source
- Cite
- Save
Citations (0)
Cantú Syndrome: Report of Nine New Cases and Expansion of the Clinical Phenotype

2011 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (57)
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome

2010 Psychiatry Research-neuroimaging
Show All
- Source
- Cite
- Save
Citations (19)
Secondary Schizophrenia: Velocardiofacial syndrome (chromosome 22q11.2 deletion syndrome) as a model of schizophrenia

2010
- Vandana Shashi
- Margaret N. Berry
Show All
- Source
- Cite
- Save
Citations (0)
Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome

2010 Psychiatry Research-neuroimaging
Show All
- Source
- Cite
- Save
Citations (39)
Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome

2006 Clinical Genetics
Show All
- Source
- Cite
- Save
Citations (69)
Schizophrenic-like deficits in nonpsychotic children and adolescents with 22Q11 deletion syndrome

2003 Schizophrenia Research
Show All
- Source
- Cite
- Save
Citations (0)
Vasomotor instability in neonates with chromosome 22q11 deletion syndrome

2003 American Journal of Medical Genetics Part A
Show All
- Source
- Cite
- Save
Citations (13)
A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27

2000 American Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (21)