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Margaret N. Berry

Observed names: M. N. Berry, M.N. Berry, Margaret Berry, Margaret N Berry, Margaret N. Berry
OpenAlex ID: A5111961706
De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay
2015 · Jessica X. Chong, Margaret J. McMillin, et al. · The American Journal of Human Genetics · 157
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Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype
2011 · Ingrid Scurr, Louise Wilson, et al. · American Journal of Medical Genetics Part A · 76
Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome
2004 · Vandana Shashi, Srirangam Muddasani, et al. · NeuroImage · 50
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Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome
2009 · Vandana Shashi, Thomas R. Kwapil, et al. · Psychiatry Research Neuroimaging · 47
The RBMX gene as a candidate for the Shashi X‐linked intellectual disability syndrome
2014 · V. Shashi, P. Xie, et al. · Clinical Genetics · 44
A Unique Form of Mental Retardation with a Distinctive Phenotype Maps to Xq26-q27
2000 · Vandana Shashi, Margaret N. Berry, et al. · The American Journal of Human Genetics · 26
A combination of physical examination and ECG detects the majority of hemodynamically significant heart defects in neonates with Down syndrome
2002 · Vandana Shashi, Margaret N. Berry, et al. · American Journal of Medical Genetics · 25
Partial duplication of 4q12q13 leads to a mild phenotype
1999 · Vandana Shashi, Margaret N. Berry, et al. · American Journal of Medical Genetics · 25
Prenatal diagnosis of complete sole trisomy 1q
2001 · Mark J. Pettenati, Margaret Berry, et al. · Prenatal Diagnosis · 24
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
2010 · Vandana Shashi, Timothy D. Howard, et al. · Psychiatry Research · 23
Vasomotor instability in neonates with chromosome 22q11 deletion syndrome
2003 · Vandana Shashi, Margaret N. Berry, et al. · American Journal of Medical Genetics Part A · 18
Prenatal interphase detection by FISH of a sex chromosome mosaicism when cytogenetics reports a pseudomosaicism
1999 · Mark J. Pettenati, Margaret N. Berry, et al. · Prenatal Diagnosis · 6
Mechanistic Approach to Understanding Psychosis Risk in Velocardiofacial Syndrome
2009 · Vandana Shashi, Margaret Berry, et al. · Current Pediatric Reviews · 4
Najjar syndrome revisited
1993 · I. T. Thomas, T. Jewett, et al. · American Journal of Medical Genetics · 4
Velocardiofacial syndrome (chromosome 22q11.2 deletion syndrome) as a model of schizophrenia
2010 · Vandana Shashi, Margaret N. Berry · Cambridge University Press eBooks
Schizophrenic-like deficits in nonpsychotic children and adolescents with 22Q11 deletion syndrome
2003 · T.R. Kwapil, V. Shashi, et al. · Schizophrenia Research
Is an elevated maternal serum uE3 MoM value in the second trimester associated with a poor pregnancy outcome?
2000 · S.A. Aufox, M.N. Berry, et al. · Genetics in Medicine
Works count: 17
Citation count: 529
H-index: 11
I10-index: 11
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