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Alexandra Blakemore

Research Profile

Genes & Molecular Sequences

Disorders

Physiology

Concepts & Ideas

Geographic Areas

France

Anatomy

Chromosomes, Human, Pair 1

Procedures

Chemicals & Drugs

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European Continental Ancestry Group

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Publications

TOP 3
Seán J Costelloe; Fotios Drenos; Julia S El-Sayed Moustafa; Anna-Liisa Hartikainen; Aroon D Hingorani; Steve E Humphries; Mika Kivimaki; Meena Kumari; Järvelin Marjo-Riitta; Jutta Palmen; Anneli Pouta; Li Qiao; Michael Thomas; Ioanna Tzoulaki; Robin G Walters; Stephen Whiting; Marjo-Riitta Järvelin; Qiao Li; Aimo Ruokonen; Ruokonen Aimo; Alexandra I F Blakemore; Lachlan J M Coin; Philippa J Talmud
Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits.
Julia S El-Sayed Moustafa; Mario Falchi; philippe froguel; Eleni Hadjigeorgiou; Peter Jacobson; David Meyre; Lars Sjöström; Rob Sladek; Sophie Visvikis-Siest; Andrew Walley; Robin G Walters; Alexessander Couto Alves; Johanna C Andersson-Assarsson; Julian E Asher; Alexandra I F Blakemore; Leonardo Bottolo; Jessica L Buxton; Lena M S Carlsson; Adam J de Smith; Christian Dina; Hariklia Eleftherohorinou; Lachlan J M Coin
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
Joram D Mul; Darleen A Sandoval; Mieke M van Haelst; Stephen C Woods; Gijs van Haaften; Suzanne I M Alsters; Denovan P Begg; Alexandra I F Blakemore; Edwin Cuppen; David A D'Alessio; Karen J Duran; Carel W le Roux; Randy J Seeley
Effect of vertical sleeve gastrectomy in melanocortin receptor 4-deficient rats.

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All Publications

2012: Seán J Costelloe; Fotios Drenos; Julia S El-Sayed Moustafa; Anna-Liisa Hartikainen; Aroon D Hingorani; Steve E Humphries; Mika Kivimaki; Meena Kumari; Järvelin Marjo-Riitta; Jutta Palmen; Anneli Pouta; Li Qiao; Michael Thomas; Ioanna Tzoulaki; Robin G Walters; Stephen Whiting; Marjo-Riitta Järvelin; Qiao Li; Aimo Ruokonen; Ruokonen Aimo; Alexandra I F Blakemore; Lachlan J M Coin; Philippa J Talmud
Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits.
Circulation. Cardiovascular genetics 2012;5(5):555-60.
2012: Julia S El-Sayed Moustafa; Mario Falchi; philippe froguel; Eleni Hadjigeorgiou; Peter Jacobson; David Meyre; Lars Sjöström; Rob Sladek; Sophie Visvikis-Siest; Andrew Walley; Robin G Walters; Alexessander Couto Alves; Johanna C Andersson-Assarsson; Julian E Asher; Alexandra I F Blakemore; Leonardo Bottolo; Jessica L Buxton; Lena M S Carlsson; Adam J de Smith; Christian Dina; Hariklia Eleftherohorinou; Lachlan J M Coin
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
Human molecular genetics 2012;21(16):3727-38.
2012: Joram D Mul; Darleen A Sandoval; Mieke M van Haelst; Stephen C Woods; Gijs van Haaften; Suzanne I M Alsters; Denovan P Begg; Alexandra I F Blakemore; Edwin Cuppen; David A D'Alessio; Karen J Duran; Carel W le Roux; Randy J Seeley
Effect of vertical sleeve gastrectomy in melanocortin receptor 4-deficient rats.
American journal of physiology. Endocrinology and metabolism 2012;303(1):E103-10.
2011: Yingrui Li; Ruibang Luo; Hanzhou Ma; Haojing Shao; Geng Tian; Jian Wang; Alexandra I F Blakemore; Lars Bolund; Hongzhi Cao; Lachlan J M Coin; Adam J de Smith; Hongli Du; Shuijian Feng; Shujia Huang; Karsten Kristiansen; Jingxiang Li; Ruiqiang Li; Songgang Li; Boxin Wu; Honglong Wu; Huanming Yang; Fan Zhang; Wei Zhang; Xiuqing Zhang; Hancheng Zheng; Hongmei Zhu; Jun Wang
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.
Nature biotechnology 2011;29(8):723-30.
2011: Anne L Trewick; Lachlan J M Coin; Adam J de Smith; philippe froguel; Gottfried Greve; Julia S El-Sayed Moustafa; Pål R Njølstad; Alexandra I F Blakemore
Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometry.
Clinical chemistry 2011;57(8):1188-95.
2011: Hariklia Eleftherohorinou; Julia S El-Sayed Moustafa; Johanna C Andersson-Assarsson; Alexandra I F Blakemore; Lena M S Carlsson; Lachlan Coin; philippe froguel; Peter Jacobson; Andrew J Walley; Robin G Walters; Mario Falchi
famCNV: copy number variant association for quantitative traits in families.
Bioinformatics (Oxford, England) 2011;27(13):1873-5.
2011: Adam J de Smith; Mieke M van Haelst; Richard J Ellis; Susan E Holder; Stewart J Payne; Sugera K Hashim; philippe froguel; Alexandra I F Blakemore
Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems.
American journal of medical genetics. Part A 2011;155A(5):1192-5.
2011: Michelle M A Fernando; Adam J de Smith; Lachlan Coin; David L Morris; philippe froguel; Jonathan Mangion; Alexandra I F Blakemore; Robert R Graham; timothy wayne behrens; Timothy J Vyse
Investigation of the HIN200 locus in UK SLE families identifies novel copy number variants.
Annals of human genetics 2011;75(3):383-97.
2011: Jessica Louise Buxton; Robin G Walters; Sophie Visvikis-Siest; David Meyre; philippe froguel; Alexandra I F Blakemore
Childhood obesity is associated with shorter leukocyte telomere length.
The Journal of clinical endocrinology and metabolism 2011;96(5):1500-5.
2010: Adam J de Smith; Anne L Trewick; Alexandra I F Blakemore
Implications of copy number variation in people with chromosomal abnormalities: potential for greater variation in copy number state may contribute to variability of phenotype.
The HUGO journal 2010;4(1-4):1-9.
2010: Alexandra I F Blakemore; philippe froguel
Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine.
Annals of the New York Academy of Sciences 2010;1214():180-9.
2010: Lachlan J M Coin; Julian E Asher; Robin G Walters; Julia S El-Sayed Moustafa; Adam J de Smith; Rob Sladek; David J Balding; philippe froguel; Alexandra I F Blakemore
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.
Nature methods 2010;7(7):541-6.
2010: Shu-Yi Su; Julian E Asher; Marjo-Riitta Jarvelin; Phillipe Froguel; Alexandra I F Blakemore; David J Balding; Lachlan J M Coin
Inferring combined CNV/SNP haplotypes from genotype data.
Bioinformatics (Oxford, England) 2010;26(11):1437-45.
2010: Claire L Price; Hafid O S Al Hassi; Nicholas R English; Alexandra I F Blakemore; Andrew J Stagg; Stella C Knight
Methylglyoxal modulates immune responses: relevance to diabetes.
Journal of cellular and molecular medicine 2010;14(6B):1806-15.
2010: Yi Fu; Zhan Chen; Alexandra I F Blakemore; Eric Orwoll; David M Cohen
Absence of AVPR2 copy number variation in eunatremic and dysnatremic subjects in non-Hispanic Caucasian populations.
Physiological genomics 2010;40(3):121-7.
2009: Ismail Al-Janabi; Maria J Arranz; Alexandra I F Blakemore; Pilar A Saiz; Margaret T Susce; Paul E A Glaser; Daniel Clark; Jose de Leon
Association study of serotonergic gene variants with antipsychotic-induced adverse reactions.
Psychiatric genetics 2009;19(6):305-11.
2009: Adam J de Smith; Carolin Purmann; Robin G Walters; Richard J Ellis; Susan E Holder; Mieke M van Haelst; Angela F Brady; Una L Fairbrother; Mehul Dattani; Julia M Keogh; Elana Henning; Giles S H Yeo; Stephen O'Rahilly; philippe froguel; I Sadaf Farooqi; Alexandra I F Blakemore
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
Human molecular genetics 2009;18(17):3257-65.
2009: Alexandra I F Blakemore; David Meyre; Jerome Delplanque; Vincent Vatin; Cecile Lecoeur; Michel Marre; Jean Tichet; Beverley Balkau; philippe froguel; Andrew J Walley
A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity.
Obesity (Silver Spring, Md.) 2009;17(8):1549-53.
2009: Sharon J Diskin; Cuiping Hou; Joseph T Glessner; Edward F Attiyeh; Marci Laudenslager; Kristopher Bosse; Kristina Cole; Yaël P Mossé; Andrew Cameron Wood; Jill E Lynch; Katlyn Pecor; Maura Diamond; Cynthia Winter; Kai Wang; Cecilia Kim; Elizabeth A Geiger; Patrick W McGrady; Alexandra I F Blakemore; Wendy B London; Tamim H Shaikh; Jonathan P Bradfield; Struan F A Grant; Hongzhe Li; Marcella Devoto; Eric R Rappaport; Hakon Hakonarson; John M Maris
Copy number variation at 1q21.1 associated with neuroblastoma.
Nature 2009;459(7249):987-91.
2009: Stéphane Cauchi; Fanny Stutzmann; Christine Cavalcanti-Proença; Emmanuelle Durand; Anneli Pouta; Anna-Liisa Hartikainen; Michel Marre; Sylviane Vol; Tuija Tammelin; Jaana Laitinen; Arturo Gonzalez-Izquierdo; Alexandra I F Blakemore; Paul Elliott; David Meyre; Beverley Balkau; Marjo-Riitta Järvelin; philippe froguel
Combined effects of MC4R and FTO common genetic variants on obesity in European general populations.
Journal of molecular medicine (Berlin, Germany) 2009;87(5):537-46.
2008: Alexandra I F Blakemore; philippe froguel
Is obesity our genetic legacy?
The Journal of clinical endocrinology and metabolism 2008;93(11 Suppl 1):S51-6.
2008: philippe froguel; Alexandra I F Blakemore
The power of the extreme in elucidating obesity.
The New England journal of medicine 2008;359(9):891-3.
2008: A J de Smith; R G Walters; philippe froguel; Alexandra I F Blakemore
Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.
Cytogenetic and genome research 2008;123(1-4):17-26.
2008: Adam J de Smith; Robin G Walters; Lachlan J M Coin; Israel Steinfeld; Zohar Yakhini; Rob Sladek; philippe froguel; Alexandra I F Blakemore
Small deletion variants have stable breakpoints commonly associated with alu elements.
PloS one 2008;3(8):e3104.
2007: Adam J de Smith; Anya Tsalenko; Nick Sampas; Alicia Scheffer; N Alice Yamada; Peter Tsang; Amir Ben-Dor; Zohar Yakhini; Richard J Ellis; Laurakay Bruhn; Stephen Laderman; philippe froguel; Alexandra I F Blakemore
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases.
Human molecular genetics 2007;16(23):2783-94.
2007: Manuela Fanciulli; Penny J Norsworthy; Enrico Petretto; Rong Dong; Lorraine Harper; Lavanya Kamesh; Joanne M Heward; S C L Gough; Adam de Smith; Alexandra I F Blakemore; philippe froguel; Catherine J Owen; Simon H S Pearce; Luis Teixeira; Loic Guillevin; Deborah S Cunninghame Graham; Charles D Pusey; H Terence Cook; Timothy J Vyse; Timothy J Aitman
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
Nature genetics 2007;39(6):721-3.
2007: Una L Fairbrother; Laszlo Tanko; Andrew J Walley; Claus Christiansen; philippe froguel; Alexandra I F Blakemore
Leptin receptor genotype at Gln223Arg is associated with body composition, BMD, and vertebral fracture in postmenopausal Danish women.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2007;22(4):544-50.
2006: Andrew J Walley; Alexandra I F Blakemore; philippe froguel
Genetics of obesity and the prediction of risk for health.
Human molecular genetics 2006;15 Spec No 2():R124-30.