Albagha OME - Search Results

1

Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.

Alonso N, Wani S, Rose L, Van't Hof RJ, Ralston SH, Albagha OME. Alonso N, et al. Among authors: albagha ome. J Bone Miner Res. 2021 Jul;36(7):1376-1386. doi: 10.1002/jbmr.4288. Epub 2021 May 6. J Bone Miner Res. 2021. PMID: 33724536 Free article.

2

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.

Shrine N, Izquierdo AG, Chen J, Packer R, Hall RJ, Guyatt AL, Batini C, Thompson RJ, Pavuluri C, Malik V, Hobbs BD, Moll M, Kim W, Tal-Singer R, Bakke P, Fawcett KA, John C, Coley K, Piga NN, Pozarickij A, Lin K, Millwood IY, Chen Z, Li L; China Kadoorie Biobank Collaborative Group; Wijnant SRA, Lahousse L, Brusselle G, Uitterlinden AG, Manichaikul A, Oelsner EC, Rich SS, Barr RG, Kerr SM, Vitart V, Brown MR, Wielscher M, Imboden M, Jeong A, Bartz TM, Gharib SA, Flexeder C, Karrasch S, Gieger C, Peters A, Stubbe B, Hu X, Ortega VE, Meyers DA, Bleecker ER, Gabriel SB, Gupta N, Smith AV, Luan J, Zhao JH, Hansen AF, Langhammer A, Willer C, Bhatta L, Porteous D, Smith BH, Campbell A, Sofer T, Lee J, Daviglus ML, Yu B, Lim E, Xu H, O'Connor GT, Thareja G, Albagha OME; Qatar Genome Program Research (QGPR) Consortium; Suhre K, Granell R, Faquih TO, Hiemstra PS, Slats AM, Mullin BH, Hui J, James A, Beilby J, Patasova K, Hysi P, Koskela JT, Wyss AB, Jin J, Sikdar S, Lee M, May-Wilson S, Pirastu N, Kentistou KA, Joshi PK, Timmers PRHJ, Williams AT, Free RC, Wang X, Morrison JL, Gilliland FD, Chen Z, Wang CA, Foong RE, Harris SE, Taylor A, Redmond P, Cook JP, Mahajan A, Lind L, Palvia… See abstract for full author list ➔ Shrine N, et al. Among authors: albagha ome. Nat Genet. 2023 Mar;55(3):410-422. doi: 10.1038/s41588-023-01314-0. Epub 2023 Mar 13. Nat Genet. 2023. PMID: 36914875 Free PMC article.

3

Estrogen receptor alpha gene polymorphisms and bone mineral density: haplotype analysis in women from the United Kingdom.

Albagha OM, McGuigan FE, Reid DM, Ralston SH. Albagha OM, et al. J Bone Miner Res. 2001 Jan;16(1):128-34. doi: 10.1359/jbmr.2001.16.1.128. J Bone Miner Res. 2001. PMID: 11149476 Free article.

4

Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women.

Albagha OM, Tasker PN, McGuigan FE, Reid DM, Ralston SH. Albagha OM, et al. Hum Mol Genet. 2002 Sep 15;11(19):2289-95. doi: 10.1093/hmg/11.19.2289. Hum Mol Genet. 2002. PMID: 12217957 Free article.

5

Association of polymorphisms of the estrogen receptor alpha gene with bone mineral density and fracture risk in women: a meta-analysis.

Ioannidis JP, Stavrou I, Trikalinos TA, Zois C, Brandi ML, Gennari L, Albagha O, Ralston SH, Tsatsoulis A; ER-alpha Genetics Meta-Analysis. Ioannidis JP, et al. J Bone Miner Res. 2002 Nov;17(11):2048-60. doi: 10.1359/jbmr.2002.17.11.2048. J Bone Miner Res. 2002. PMID: 12412813 Free article.

6

Genetic determinants of susceptibility to osteoporosis.

Albagha OM, Ralston SH. Albagha OM, et al. Endocrinol Metab Clin North Am. 2003 Mar;32(1):65-81, vi. doi: 10.1016/s0889-8529(02)00059-2. Endocrinol Metab Clin North Am. 2003. PMID: 12699293 Review.

7

Type II benign osteopetrosis (Albers-Schönberg disease) caused by a novel mutation in CLCN7 presenting with unusual clinical manifestations.

Letizia C, Taranta A, Migliaccio S, Caliumi C, Diacinti D, Delfini E, D'Erasmo E, Iacobini M, Roggini M, Albagha OM, Ralston SH, Teti A. Letizia C, et al. Calcif Tissue Int. 2004 Jan;74(1):42-6. doi: 10.1007/s00223-002-1087-5. Epub 2003 Nov 26. Calcif Tissue Int. 2004. PMID: 14564431

8

Association between TNFRSF1B polymorphisms and bone mineral density, bone loss and fracture.

Tasker PN, Albagha OM, Masson CB, Reid DM, Ralston SH. Tasker PN, et al. Osteoporos Int. 2004 Nov;15(11):903-8. doi: 10.1007/s00198-004-1617-2. Epub 2004 Apr 8. Osteoporos Int. 2004. PMID: 15071724

9

Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes.

Ioannidis JP, Ralston SH, Bennett ST, Brandi ML, Grinberg D, Karassa FB, Langdahl B, van Meurs JB, Mosekilde L, Scollen S, Albagha OM, Bustamante M, Carey AH, Dunning AM, Enjuanes A, van Leeuwen JP, Mavilia C, Masi L, McGuigan FE, Nogues X, Pols HA, Reid DM, Schuit SC, Sherlock RE, Uitterlinden AG; GENOMOS Study. Ioannidis JP, et al. JAMA. 2004 Nov 3;292(17):2105-14. doi: 10.1001/jama.292.17.2105. JAMA. 2004. PMID: 15523071

10

Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone.

Albagha OM, Pettersson U, Stewart A, McGuigan FE, MacDonald HM, Reid DM, Ralston SH. Albagha OM, et al. J Med Genet. 2005 Mar;42(3):240-6. doi: 10.1136/jmg.2004.023895. J Med Genet. 2005. PMID: 15744038 Free PMC article.

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