Robert Colin Carter

Dr. Robert Colin Carter

Institute of Human Nutrition and Departments of Emergency Medicine and Pediatrics, Columbia University Irving Medical Center, New York, NY, USA

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2016 in Pediatrics
Verified
Journal Article
Open access
PDF file
RCRobert Colin Carter
Robert Colin Carter
JJJoseph L. Jacobson
Joseph L. Jacobson
CMChristopher D. Molteno
Christopher D. Molteno
NDNeil C. Dodge
Neil C. Dodge
EMErnesta M. Meintjes
Ernesta M. Meintjes
SJSandra W. Jacobson
Sandra W. Jacobson
BACKGROUND: Although both fetal and long-term growth restriction are well documented in fetal alcohol spectrum disorders, effects on pattern of growth trajectory have not been characterized. Furthermore, the degree to which growth trajectories are related to fetal alcohol-related neurocognitive deficits is unknown. METHODS: Ninety-three heavy drinking pregnant women and 64 controls were recruited at initiation of prenatal care in Cape Town, South Africa. Small for gestational age (SGA) was defined as birth weight <10th percentile. Length/height, weight, and head circumference were measured at 6.5 and 12 months and 5, 9, and 13 years. Four growth trajectories were identified: SGA with long-term postnatal growth restriction (length/height-for-age <10th percentile through 13 years); SGA with catch-up growth; no SGA or postnatal growth restriction; and late-onset postnatal stunting. IQ was assessed at 5 and 10 years, and learning, memory, and executive function at 10 years. RESULTS: Children born SGA with postnatal growth restriction were most heavily exposed. Exposure was intermediate for those born SGA with catch-up growth and lowest for those without prenatal or postnatal growth restriction. Effects on neurocognition were strongest in children with both prenatal and long-term growth restriction, more moderate in those with fetal growth restriction and postnatal catch-up, and weakest in those without growth restriction. CONCLUSIONS: These findings validate the use of growth restriction in the diagnosis of fetal alcohol spectrum disorders and identify growth trajectory as a biomarker of which heavily exposed children are at greatest risk for cognitive developmental deficits.

3 April 2016 in Alcohol, Clinical and Experimental Research
Verified
Journal Article
Closed access
PDF file
RCRobert Colin Carter
Robert Colin Carter
HWHelen Wainwright
Helen Wainwright
CMChristopher D. Molteno
Christopher D. Molteno
MGMichael K. Georgieff
Michael K. Georgieff
NDNeil C. Dodge
Neil C. Dodge
SJSandra W. Jacobson
Sandra W. Jacobson

1 March 2017 in Alcohol, Clinical and Experimental Research
Verified
Journal Article
Closed access
PDF file
SJSandra W Jacobson
Sandra W Jacobson
JJJoseph L. Jacobson
Joseph L. Jacobson
CMChristopher D. Molteno
Christopher D. Molteno
CWChristopher M.R. Warton
Christopher M.R. Warton
PWPia Wintermark
Pia Wintermark
EMErnesta M. Meintjes
Ernesta M. Meintjes

31 October 2017 in Alcohol, Clinical and Experimental Research
Verified
Journal Article
Closed access
PDF file
RCRobert Colin Carter
Robert Colin Carter
MSMarjanne Senekal
Marjanne Senekal
NDNeil C. Dodge
Neil C. Dodge
LBLori J. Bechard
Lori J. Bechard
EMErnesta M. Meintjes
Ernesta M. Meintjes
SJSandra W Jacobson
Sandra W Jacobson

2 August 2021 in Alcohol, Clinical and Experimental Research
Verified
Journal Article
Closed access
PDF file
FWFleur L. Warton
Fleur L. Warton
CMChristopher D. Molteno
Christopher D. Molteno
CWChristopher M. R. Warton
Christopher M. R. Warton
PWPia Wintermark
Pia Wintermark
NLNadine M. Lindinger
Nadine M. Lindinger
EMErnesta M. Meintjes
Ernesta M. Meintjes