Anne M. Molloy

Anne M. Molloy


Research Focus & Metrics

Academic Career Length

49Years (1978-Present)

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

Representative Publications

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2 May 2010 in Nature Genetics
Verified
Journal Article
Open access
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TBTerri H Beaty
Terri H Beaty
JMJeffrey C Murray
Jeffrey C Murray
MMMary L Marazita
Mary L Marazita
RMRonald G Munger
Ronald G Munger
IRIngo Ruczinski
Ingo Ruczinski
ASAlan F Scott
Alan F Scott
Terri Beaty and colleagues report a genome-wide association study of cleft lip with/without cleft palate. They identified variants near MAFB and ABCA4 associated with risk of this birth defect in case-parent trios of European and Asian ancestry. Case-parent trios were used in a genome-wide association study of cleft lip with and without cleft palate. SNPs near two genes not previously associated with cleft lip with and without cleft palate (MAFB, most significant SNP rs13041247, with odds ratio (OR) per minor allele = 0.704, 95% CI 0.635–0.778, P = 1.44 × 10−11; and ABCA4, most significant SNP rs560426, with OR = 1.432, 95% CI 1.292–1.587, P = 5.01 × 10−12) and two previously identified regions (at chromosome 8q24 and IRF6) attained genome-wide significance. Stratifying trios into European and Asian ancestry groups revealed differences in statistical significance, although estimated effect sizes remained similar. Replication studies from several populations showed confirming evidence, with families of European ancestry giving stronger evidence for markers in 8q24, whereas Asian families showed stronger evidence for association with MAFB and ABCA4. Expression studies support a role for MAFB in palatal development.

1 July 2015 in The Journal of Nutrition
Verified
Journal Article
Closed access
PDF file
LBLynn Bailey
Lynn Bailey
PSPatrick J Stover
Patrick J Stover
HMHelene Mcnulty
Helene Mcnulty
MFMichael F Fenech
Michael F Fenech
JGJesse F Gregory
Jesse F Gregory
DRDan Raiten
Dan Raiten
The Biomarkers of Nutrition for Development (BOND) project is designed to provide evidence-based advice to anyone with an interest in the role of nutr

18 June 2014 in British Journal of Haematology
Verified
Journal Article
Closed access
PDF file
VDVinod Devalia
Vinod Devalia
MHMalcolm S. Hamilton
Malcolm S. Hamilton
AMAnne M. Molloy
Anne M. Molloy
THthe British Committee for Standards in Haematology
the British Committee for Standards in Haematology


22 June 2008 in Food and Nutrition Bulletin
Verified
Journal Article
Open access
PDF file
AMAnne M. Molloy
Anne M. Molloy
PKPeadar N. Kirke
Peadar N. Kirke
LBLawrence C. Brody
Lawrence C. Brody
JSJohn M. Scott
John M. Scott
JMJames Mills
James Mills
The importance of folate in reproduction can be appreciated by considering that the existence of the vitamin was first suspected from efforts to explain a potentially fatal megaloblastic anemia in young pregnant women in India. Today, low maternal folate status during pregnancy and lactation remains a significant cause of maternal morbidity in some communities. The folate status of the neonate tends to be protected at the expense of maternal stores; nevertheless, there is mounting evidence that inadequate maternal folate status during pregnancy may lead to low infant birthweight, thereby conferring risk of developmental and long-term adverse health outcomes. Moreover, folate-related anemia during childhood and adolescence might predispose children to further infections and disease. The role of folic acid in prevention of neural tube defects (NTD) is now established, and several studies suggest that this protection may extend to some other birth defects. In terms of maternal health, clinical vitamin B12 deficiency may be a cause of infertility or recurrent spontaneous abortion. Starting pregnancy with an inadequate vitamin B12 status may increase risk of birth defects such as NTD, and may contribute to preterm delivery, although this needs further evaluation. Furthermore, inadequate vitamin B12 status in the mother may lead to frank deficiency in the infant if sufficient fetal stores of vitamin B12 are not laid down during pregnancy or are not available in breastmilk. However, the implications of starting pregnancy and lactation with low vitamin B12 status have not been sufficiently researched.

1 May 1997 in The Lancet
Verified
Journal Article
Closed access
AMAnne M. Molloy
Anne M. Molloy
SDSean Daly
Sean Daly
JMJames Mills
James Mills
PKPeadar N Kirke
Peadar N Kirke
AWAlexander S Whitehead
Alexander S Whitehead
JSJohn M Scott
John M Scott