Jess Buxton
Jess Buxton
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Cited by
Cited by
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3'end of a transcript encoding a protein kinase family member.
JD Brook, ME McCurrach, HG Harley, AJ Buckler, D Church, H Aburatani, ...
Cell 68 (4), 799, 1992
Identification of seven loci affecting mean telomere length and their association with disease
V Codd, CP Nelson, E Albrecht, M Mangino, J Deelen, JL Buxton, ...
Nature genetics 45 (4), 422-427, 2013
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
J Buxton, P Shelbourne, J Davies, C Jones, TV Tongeren, C Aslanidis, ...
Nature 355 (6360), 547-548, 1992
Cloning of the essential myotonic dystrophy region and mapping of the putative defect
C Aslanidis, G Jansen, C Amemiya, G Shutler, M Mahadevan, C Tsilfidis, ...
Nature 355 (6360), 548-551, 1992
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2
RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ...
Nature 463 (7281), 671-675, 2010
A genome-wide association meta-analysis identifies new childhood obesity loci
Nature genetics 44 (5), 526-531, 2012
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
L Paternoster, M Standl, CM Chen, A Ramasamy, K Bønnelykke, L Duijts, ...
Nature genetics 44 (2), 187-192, 2012
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
M Horikoshi, H Yaghootkar, DO Mook-Kanamori, U Sovio, HR Taal, ...
Nature genetics 45 (1), 76-82, 2013
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
B Dittrich, K Buiting, B Korn, S Rickard, J Buxton, S Saitoh, RD Nicholls, ...
Nature genetics 14 (2), 163-170, 1996
Expansion of the Gene Ontology knowledgebase and resources
S Carbon, H Dietze, SE Lewis, CJ Mungall, MC Munoz-Torres, S Basu, ...
Nucleic acids research 45 (D1), 2017
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
S Saitoh, K Buiting, PK Rogan, JL Buxton, DJ Driscoll, J Arnemann, ...
Proceedings of the National Academy of Sciences 93 (15), 7811-7815, 1996
Childhood obesity is associated with shorter leukocyte telomere length
JL Buxton, RG Walters, S Visvikis-Siest, D Meyre, P Froguel, ...
The Journal of Clinical Endocrinology & Metabolism 96 (5), 1500-1505, 2011
Common variants at 12q15 and 12q24 are associated with infant head circumference
HR Taal, B St Pourcain, E Thiering, S Das, DO Mook-Kanamori, ...
Nature genetics 44 (5), 532-538, 2012
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype
P Shelbourne, R Winqvist, E Kunert, J Davies, J Leisti, H Thiele, ...
Human molecular genetics 1 (7), 467-473, 1992
Genome-wide association analysis in humans links nucleotide metabolism to leukocyte telomere length
C Li, S Stoma, LA Lotta, S Warner, E Albrecht, A Allione, PP Arp, L Broer, ...
The American Journal of Human Genetics 106 (3), 389-404, 2020
Telomere length in circulating leukocytes is associated with lung function and disease
E Albrecht, E Sillanpää, S Karrasch, AC Alves, V Codd, I Hovatta, ...
European Respiratory Journal 43 (4), 983-992, 2014
A novel common variant in DCST2 is associated with length in early life and height in adulthood
RJP van der Valk, E Kreiner-Møller, MN Kooijman, M Guxens, ...
Human molecular genetics 24 (4), 1155-1168, 2015
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.
J Davies, H Yamagata, P Shelbourne, J Buxton, T Ogihara, P Nokelainen, ...
Journal of medical genetics 29 (11), 766-769, 1992
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
A Couto Alves, NMG De Silva, V Karhunen, U Sovio, S Das, HR Taal, ...
Science Advances 5 (9), eaaw3095, 2019
Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker
P Shelbourne, J Davies, J Buxton, M Anvret, E Blennow, M Bonduelle, ...
New England Journal of Medicine 328 (7), 471-475, 1993
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