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Plasma lipids and growth faltering
Gerard Bryan Gonzales, Daniella Brals, Bakary Sonko, Fatou Sosseh, Andrew M Prentice, Sophie E Moore, Albert Koulman
Oct 18, 2021
[Figure: see text].
Published by: Science advances
Timing of the Infancy-Childhood Growth Transition in Rural Gambia
Robin M. Bernstein, G. Kesler O'Connor, Eric A. Vance, Nabeel Affara, Saikou Drammeh, David B. Dunger, Abdoulie Faal, Ken K. Ong, Fatou Sosseh, Andrew M. Prentice, Sophie E. Moore
Apr 07, 2020
The Karlberg model of human growth describes the infancy, childhood, and puberty (ICP) stages as continuous and overlapping, and defined by transitions driven by sequential additional effects of several endocrine factors that...
Timing of the Infancy-Childhood Growth Transition in Rural Gambia.
Robin M Bernstein, G Kesler O'Connor, Eric A Vance, Nabeel Affara, Saikou Drammeh, David B Dunger, Abdoulie Faal, Ken K Ong, Fatou Sosseh, Andrew M Prentice, Sophie E Moore
May 09, 2020
The Karlberg model of human growth describes the infancy, childhood, and puberty (ICP) stages as continuous and overlapping, and defined by transitions driven by sequential additional effects of several endocrine factors that...
Published by: Frontiers in endocrinology
A Novel method for the identification and quantification of weight faltering.
Daniel J Naumenko, James Dykes, G Kesler O'Connor, Zofia Stanley, Nabeel Affara, Andrew M Doel, Saikou Drammeh, David B Dunger, Abdoulie Faal, Ken K Ong, Fatou Sosseh, Andrew M Prentice, Sophie E Moore, Robin M Bernstein
Jan 19, 2021
OBJECTIVE: We describe a new method for identifying and quantifying the magnitude and rate of short-term weight faltering episodes, and assess how (a) these episodes relate to broader growth outcomes, and (b) different data...
Timing of the Infancy-Childhood Growth Transition in Rural Gambia.
Robin M Bernstein, G Kesler O'Connor, Eric A Vance, Nabeel Affara, Saikou Drammeh, David B Dunger, Abdoulie Faal, Ken K Ong, Fatou Sosseh, Andrew M Prentice, Sophie E Moore
May 26, 2020
The Karlberg model of human growth describes the infancy, childhood, and puberty (ICP) stages as continuous and overlapping, and defined by transitions driven by sequential additional effects of several endocrine factors that...
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
Lisa Borghini, Eileen Png, Alexander Binder, Victoria J Wright, Ellie Pinnock, Ronald de Groot, Jan Hazelzet, Marieke Emonts, Michiel Van der Flier, Luregn J Schlapbach, Suzanne Anderson, Fatou Secka, Antonio Salas, Colin Fink, Enitan D Carrol, Andrew J Pollard, Lachlan J Coin, Taco W Kuijpers, Federico Martinon-Torres, Werner Zenz, Michael Levin, Martin L Hibberd, Sonia Davila, EUCLIDS consortium
Nov 17, 2020
Non-coding genetic variants play an important role in driving susceptibility to complex diseases but their characterization remains challenging. Here, we employed a novel approach to interrogate the genetic risk of such...
Case-Control Studies Cohort Studies Genetic Association Studies Genetic Predisposition to Disease Genomics High-Throughput Nucleotide Sequencing Humans Hypopharyngeal Neoplasms Meningococcal Infections Neisseria meningitidis Phenotype Polymorphism Single Nucleotide Regulatory Sequences Nucleic Acid Tumor Cells Cultured
The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia.
John Muthii Muriuki, Alexander J Mentzer, Gavin Band, James J Gilchrist, Tommy Carstensen, Swaib A Lule, Morgan M Goheen, Fatou Joof, Wandia Kimita, Reagan Mogire, Clare L Cutland, Amidou Diarra, Anna Rautanen, Cristina Pomilla, Deepti Gurdasani, Kirk Rockett, Neema Mturi, Francis M Ndungu, J Anthony G Scott, Sodiomon B Sirima, Alireza Morovat, Andrew M Prentice, Shabir A Madhi, Emily L Webb, Alison M Elliott, Philip Bejon, Manjinder S Sandhu, Adrian VS Hill, Dominic P Kwiatkowski, Thomas N Williams, Carla Cerami, Sarah H Atkinson
Oct 03, 2019
Iron acquisition is critical for life. Ferroportin (FPN) exports iron from mature erythrocytes, and deletion of the Fpn gene results in hemolytic anemia and increased fatality in malaria-infected mice. The FPN Q248H mutation...