Publications by authors named "Kathryn Robson"

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Paths and timings of the peopling of Polynesia inferred from genomic networks.
Alexander G Ioannidis, Javier Blanco-Portillo, Karla Sandoval, Erika Hagelberg, Carmina Barberena-Jonas, Adrian V S Hill, Juan Esteban Rodríguez-Rodríguez, Keolu Fox, Kathryn Robson, Sonia Haoa-Cardinali

Nature· September 2021

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Native American gene flow into Polynesia predating Easter Island settlement.
Alexander G Ioannidis, Javier Blanco-Portillo, Karla Sandoval, Erika Hagelberg, Juan Francisco Miquel-Poblete, J Víctor Moreno-Mayar, Juan Esteban Rodríguez-Rodríguez, Consuelo D Quinto-Cortés, Kathryn Auckland, Tom Parks

Nature· July 2020

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Ancient DNA reveals five streams of migration into Micronesia and matrilocality in early Pacific seafarers.
Yue-Chen Liu, Rosalind Hunter-Anderson, Olivia Cheronet, Joanne Eakin, Frank Camacho, Kathryn Robson

Science· July 2022

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A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes.
Paul Bastard, Kuang-Chih Hsiao, Qian Zhang, Jeremy Choin, Emma Best, Kathryn Robson

J Exp Med· June 2022

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The p.H63D allele of the HFE gene protects against low iron stores in Sri Lanka.
Angela Allen, Anuja Premawardhena, Stephen Allen, Rexan Rodrigo, Aresha Manamperi, Kathryn Robson

Blood Cells Mol Dis· May 2019

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Language continuity despite population replacement in Remote Oceania.
Cosimo Posth, Kathrin Nägele, Heidi Colleran, Frédérique Valentin, Stuart Bedford, Kathryn J Robson

Nat Ecol Evol· April 2018

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Population Turnover in Remote Oceania Shortly after Initial Settlement.
Mark Lipson, Pontus Skoglund, Matthew Spriggs, Frederique Valentin, Stuart Bedford, Kathryn Robson

Curr Biol· April 2018

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A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea.
Anders Bergström, Stephen J Oppenheimer, Alexander J Mentzer, Kathryn Auckland, Kathryn Robson

Science· September 2017

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Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania.
Tom Parks, Mariana M Mirabel, Joseph Kado, Kathryn Auckland, Jaroslaw Nowak, Kathryn J Robson

Nat Commun· May 2017

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Heterozygous BMP6 Variants Coupled With HFE Variants.
Patricia Bignell, Wale Atoyebi, Kathryn Robson

Gastroenterology· October 2016

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Distinct gene expression program dynamics during erythropoiesis from human induced pluripotent stem cells compared with adult and cord blood progenitors.
Alison T Merryweather-Clarke, Alex J Tipping, Abigail A Lamikanra, Rui Fa, Basel Abu-Jamous, Kathryn J H Robson

BMC Genomics· October 2016

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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Jenny C Taylor, Hilary C Martin, Stefano Lise, John Broxholme, Jean-Baptiste Cazier, Kathryn Robson

Nat Genet· July 2015

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Coeliac patients are undiagnosed at routine upper endoscopy.
Kathryn Robson, Michelle Alizart, Jarad Martin, Robyn Nagel

PLoS One· November 2014

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Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
Martin Breuss, Julian Ik-Tsen Heng, Karine Poirier, Guoling Tian, Xavier Hubert Jaglin, Kathryn J H Robson

Cell Rep· December 2012

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Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project.
Donald J Lehmann, Maaike Schuur, Donald R Warden, Naomi Hammond, Olivia Belbin, Kathryn Robson

Neurobiol Aging· January 2012

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Global gene expression analysis of human erythroid progenitors.
Alison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, Nicki Gray, Kevin Clark, Kathryn J H Robson

Blood· March 2011

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A novel missense mutation c.470 A>C (p.D157A) in the SLC40A1 gene as a cause of ferroportin disease in a family with hyperferritinaemia.
Khalid Saja, Patricia Bignell, Kathryn Robson, Drew Provan

Br J Haematol· June 2010

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A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient.
Jennifer J Pointon, Chun Yu Lok, Jeremy D Shearman, Richard J Suckling, Jacques Rochette, Kathryn J H Robson

Blood Cells Mol Dis· October 2009

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In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.
Lisa M Schimanski, Hal Drakesmith, Emma Sweetland, Judy Bastin, Dellel Rezgui, Kathryn J H Robson

Blood Cells Mol Dis· October 2009

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Iron overload in the Asian community.
Chun Yu Lok, Alison T Merryweather-Clarke, Vip Viprakasit, Yingyong Chinthammitr, Somdet Srichairatanakool, Kathryn J H Robson

Blood· July 2009

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Malarial anemia and STAT6.
Kathryn J H Robson, David J Weatherall

Haematologica· February 2009

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Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.
Patricia Aguilar-Martinez, Chun Yu Lok, Séverine Cunat, Estelle Cadet, Kathryn Robson

Haematologica· March 2007

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Cellular reactivity to the p. Falciparum protein trap in adult kenyans: novel epitopes, complex cytokine patterns, and the impact of natural antigenic variation.
Katie L Flanagan, Magdalena Plebanski, Kennedy Odhiambo, Eric Sheu, Tabitha Mwangi, Kathryn J Robson

Am J Trop Med Hyg· March 2006

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Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.
M G Zaahl, Alison T Merryweather-Clarke, Maritha J Kotze, Schalk van der Merwe, Louise Warnich, Kathryn J H Robson

Hum Genet· December 2005

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Gene symbol: DCYTB/CYBRD1. Disease: primary iron overload.
M G Zaahl, Alison T Merryweather-Clarke, Maritha J Kotze, Schalk van der Merwe, Louise Warnich, Kathryn J H Robson

Hum Genet· December 2005

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