Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Alonso Lopez Nerea |

** = Publikationen gelistet in SCI/SSCI/Pubmed

2025

Originalarbeit (Zeitschrift)

** Herrmann, M; Keppel, MH; Zelzer, S; Alonso, N; Cavalier, E; Kleber, M; Enko, D; Scharnagl, H; Pilz, S; März, W The role of functional vitamin D deficiency and low vitamin D reservoirs in relation to cardiovascular health and mortality.
Clin Chem Lab Med. 2025; 63(1):208-219 Doi: 10.1515/cclm-2024-0391
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** Larraz-Prieto, B; Lind, LH; Olesen, JB; Azfer, A; Hansen, MS; Frost, M; Jafari, A; Ralston, SH; Søe, K; Alonso, N CXCR4 is a response gene for parathyroid hormone which affects osteoblast and osteoclast function in vitro.
Bone Joint Res. 2025; 14(5):463-476 Doi: 10.1302/2046-3758.145.BJR-2024-0167.R1 [OPEN ACCESS]
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2024

Originalarbeit (Zeitschrift)

** Alonso, N; Almer, G; Semeraro, MD; Rodriguez-Blanco, G; Fauler, G; Anders, I; Ritter, G; Vom, Scheidt, A; Hammer, N; Gruber, HJ; Herrmann, M Impact of High-Fat Diet and Exercise on Bone and Bile Acid Metabolism in Rats.
NUTRIENTS. 2024; 16(11): Doi: 10.3390/nu16111744 [OPEN ACCESS]
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** Zelzer, S; Meinitzer, A; Enko, D; Markis, K; Tournis, S; Trifonidi, I; Chronopoulos, E; Spanou, L; Alonso, N; Keppel, M; Herrmann, M Vitamin D and vitamin K status in postmenopausal women with normal and low bone mineral density.
Clin Chem Lab Med. 2024; 62(7):1402-1410 Doi: 10.1515/cclm-2023-1443
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Übersichtsarbeit

** Foessl, I; Ackert-Bicknell, CL; Kague, E; Laskou, F; Jakob, F; Karasik, D; Obermayer-Pietsch, B; Alonso, N; Bjørnerem, Å; Brandi, ML; Busse, B; Calado, Â; Cebi, AH; Christou, M; Curran, KM; Hald, JD; Semeraro, MD; Douni, E; Duncan, EL; Duran, I; Formosa, MM; Gabet, Y; Ghatan, S; Gkitakou, A; Hassler, EM; Högler, W; Heino, TJ; Hendrickx, G; Khashayar, P; Kiel, DP; Koromani, F; Langdahl, B; Lopes, P; Mäkitie, O; Maurizi, A; Medina-Gomez, C; Ntzani, E; Ohlsson, C; Prijatelj, V; Rabionet, R; Reppe, S; Rivadeneira, F; Roshchupkin, G; Sharma, N; Søe, K; Styrkarsdottir, U; Szulc, P; Teti, A; Tobias, J; Valjevac, A; van, de, Peppel, J; van, der, Eerden, B; van, Rietbergen, B; Zekic, T; Zillikens, MC, , Co-authors A perspective on muscle phenotyping in musculoskeletal research.
Trends Endocrinol Metab. 2024; 35(6):478-489 Doi: 10.1016/j.tem.2024.01.004
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** Herrmann, M; Rodriguez-Blanco, G; Balasso, M; Sobolewska, K; Semeraro, MD; Alonso, N; Herrmann, W The role of bile acid metabolism in bone and muscle: from analytics to mechanisms.
Crit Rev Clin Lab Sci. 2024; 1-19 Doi: 10.1080/10408363.2024.2323132
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2023

Originalarbeit (Zeitschrift)

** Alonso, N; Albagha, OME; Azfer, A; Larraz-Prieto, B; Berg, K; Riches, PL; Ostanek, B; Kocjan, T; Marc, J; Langdahl, BL; Ralston, SH Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy.
Ann Rheum Dis. 2023; Doi: 10.1136/ard-2022-223618
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Übersichtsarbeit

** Alonso, N; Meinitzer, A; Fritz-Petrin, E; Enko, D; Herrmann, M Role of Vitamin K in Bone and Muscle Metabolism.
Calcif Tissue Int. 2023; 112(2):178-196 Doi: 10.1007/s00223-022-00955-3 [OPEN ACCESS]
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2022

Originalarbeit (Zeitschrift)

** Meinitzer, A; Enko, D; Zelzer, S; Prüller, F; Alonso, N; Fritz-Petrin, E; Herrmann, M Development of a liquid chromatography mass spectrometry method for the determination of vitamin K1, menaquinone-4, menaquinone-7 and vitamin K1-2,3 epoxide in serum of individuals without vitamin K supplements.
Clin Chem Lab Med. 2022; 60(7):1011-1019 Doi: 10.1515/cclm-2022-0192
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Übersichtsarbeit

** Alonso, N; Zelzer, S; Eibinger, G; Herrmann, M Vitamin D Metabolites: Analytical Challenges and Clinical Relevance
CALCIFIED TISSUE INT. 2022; Doi: 10.1007/s00223-022-00961-5 [OPEN ACCESS]
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2021

Originalarbeit (Zeitschrift)

** Alonso, N; Wani, S; Rose, L; Van't, Hof, RJ; Ralston, SH; Albagha, OME Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.
J Bone Miner Res. 2021; 36(7):1376-1386 Doi: 10.1002/jbmr.4288
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** Donáth, J; Balla, B; Pálinkás, M; Rásonyi, R; Vastag, G; Alonso, N; Prieto, BL; Vallet, M; Ralston, SH; Poór, G Pattern of SQSTM1 Gene Variants in a Hungarian Cohort of Paget's Disease of Bone.
Calcif Tissue Int. 2021; 108(2): 159-164. Doi: 10.1007/s00223-020-00758-4 [OPEN ACCESS]
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Übersichtsarbeit

** Hauser, B; Alonso, N; Riches, PL Review of Current Real-World Experience with Teriparatide as Treatment of Osteoporosis in Different Patient Groups
J CLIN MED. 2021; 10(7): 1403 Doi: 10.3390/jcm10071403 [OPEN ACCESS]
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** Koromani, F; Alonso, N; Alves, I; Brandi, ML; Foessl, I; Formosa, MM; Morgenstern, MF; Karasik, D; Kolev, M; Makitie, O; Ntzani, E; Pietsch, BO; Ohlsson, C; Rauner, M; Soe, K; Soldatovic, I; Teti, A; Valjevac, A; Rivadeneira, F The "GEnomics of Musculo Skeletal Traits TranslatiOnal NEtwork": Origins, Rationale, Organization, and Prospects.
Front Endocrinol (Lausanne). 2021; 12:709815 Doi: 10.3389/fendo.2021.709815 [OPEN ACCESS]
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** Tobias, JH; Duncan, EL; Kague, E; Hammond, CL; Gregson, CL; Bassett, D; Williams, GR; Min, JL; Gaunt, TR; Karasik, D; Ohlsson, C; Rivadeneira, F; Edwards, JR; Hannan, FM; Kemp, JP; Gilbert, SJ; Alonso, N; Hassan, N; Compston, JE; Ralston, SH Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020.
Front Endocrinol (Lausanne). 2021; 11: 630875 Doi: 10.3389/fendo.2020.630875 [OPEN ACCESS]
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2020

Originalarbeit (Zeitschrift)

** Alonso, N; Larraz-Prieto, B; Berg, K; Lambert, Z; Redmond, P; Harris, SE; Deary, IJ; Pugh, C; Prendergast, J; Ralston, SH Loss-of-Function Mutations in the ALPL Gene Presenting with Adult Onset Osteoporosis and Low Serum Concentrations of Total Alkaline Phosphatase.
J Bone Miner Res. 2020; 35(4):657-661 Doi: 10.1002/jbmr.3928 [OPEN ACCESS]
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** Bhadada, SK; Pal, R; Dhiman, V; Alonso, N; Ralston, SH; Kaur, S; Gupta, R Adult hypophosphatasia with a novel ALPL mutation: Report of an Indian kindred.
Bone Rep. 2020; 12: 100247 Doi: 10.1016/j.bonr.2020.100247 (- Case Report) [OPEN ACCESS]
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2018

Originalarbeit (Zeitschrift)

** Alonso, N; Canueto, J; Ciria, S; Bueno, E; Palacios-Alvarez, I; Alegre, M; Badenas, C; Barreiro, A; Pena, L; Maldonado, C; Nespeira-Jato, MV; Pena-Penabad, C; Azon, A; Gavrilova, M; Ferrer, I; Sanmartin, O; Robles, L; Hernandez-Martin, A; Urioste, M; Puig, S; Puig, L; Gonzalez-Sarmiento, R Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome
BRIT J DERMATOL. 2018; 178(1): 198-206. Doi: 10.1111/bjd.15835
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** Alonso, N; Estrada, K; Albagha, OME; Herrera, L; Reppe, S; Olstad, OK; Gautvik, KM; Ryan, NM; Evans, KL; Nielson, CM; Hsu, YH; Kiel, DP; Markozannes, G; Ntzani, EE; Evangelou, E; Feenstra, B; Liu, X; Melbye, M; Masi, L; Brandi, ML; Riches, P; Daroszewska, A; Olmos, JM; Valero, C; Castillo, J; Riancho, JA; Husted, LB; Langdahl, BL; Brown, MA; Duncan, EL; Kaptoge, S; Khaw, KT; Usategui-Martín, R; Del, Pino-Montes, J; González-Sarmiento, R; Lewis, JR; Prince, RL; D'Amelio, P; García-Giralt, N; Nogués, X; Mencej-Bedrac, S; Marc, J; Wolstein, O; Eisman, JA; Oei, L; Medina-Gómez, C; Schraut, KE; Navarro, P; Wilson, JF; Davies, G; Starr, J; Deary, I; Tanaka, T; Ferrucci, L; Gianfrancesco, F; Gennari, L; Lucas, G; Elosua, R; Uitterlinden, AG; Rivadeneira, F; Ralston, SH Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Ann Rheum Dis. 2018; 77(3): 378-385. Doi: 10.1136/annrheumdis-2017-212469 [OPEN ACCESS]
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** Trajanoska, K; Morris, JA; Oei, L; Zheng, HF; Evans, DM; Kiel, DP; Ohlsson, C; Richards, JB; Rivadeneira, F; GEFOS/GENOMOS Consortium Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study
BMJ-BRIT MED J. 2018; 362: k3225 Doi: 10.1136/bmj.k3225 [OPEN ACCESS]
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2017

Übersichtsarbeit

** Alonso, N; Calero-Paniagua, I; del Pino-Montes, J Clinical and Genetic Advances in Paget's Disease of Bone: a Review
CLIN REV BONE MINER. 2017; 15(1): 37-48. Doi: 10.1007/s12018-016-9226-0 [OPEN ACCESS]
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2016

Originalarbeit (Zeitschrift)

** Nielson, CM; Liu, CT; Smith, AV; Ackert-Bicknell, CL; Reppe, S; Jakobsdottir, J; Wassel, C; Register, TC; Oei, L; Alonso, N; Oei, EH; Parimi, N; Samelson, EJ; Nalls, MA; Zmuda, J; Lang, T; Bouxsein, M; Latourelle, J; Claussnitzer, M; Siggeirsdottir, K; Srikanth, P; Lorentzen, E; Vandenput, L; Langefeld, C; Raffield, L; Terry, G; Cox, AJ; Allison, MA; Criqui, MH; Bowden, D; Ikram, MA; Mellström, D; Karlsson, MK; Carr, J; Budoff, M; Phillips, C; Cupples, LA; Chou, WC; Myers, RH; Ralston, SH; Gautvik, KM; Cawthon, PM; Cummings, S; Karasik, D; Rivadeneira, F; Gudnason, V; Orwoll, ES; Harris, TB; Ohlsson, C; Kiel, DP; Hsu, YH Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
J Bone Miner Res. 2016; 31(12): 2085-2097. Doi: 10.1002/jbmr.2913 [OPEN ACCESS]
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2015

Originalarbeit (Zeitschrift)

** Alonso, N; Lucas, G; Hysi, P Big data challenges in bone research: genome-wide association studies and next-generation sequencing
BONEKEY REP. 2015; 4: 635 Doi: 10.1038/bonekey.2015.2 [OPEN ACCESS]
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** Alonso, N; Soares, DC; V, McCloskey, E; Summers, GD; Ralston, SH; Gregson, CL Atypical femoral fracture in osteoporosis pseudoglioma syndrome associated with two novel compound heterozygous mutations in LRP5.
J Bone Miner Res. 2015; 30(4): 615-20. Doi: 10.1002/jbmr.2403 (- Case Report)
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** Shungin, D; Winkler, TW; Croteau-Chonka, DC; Ferreira, T; Locke, AE; Mägi, R; Strawbridge, RJ; Pers, TH; Fischer, K; Justice, AE; Workalemahu, T; Wu, JMW; Buchkovich, ML; Heard-Costa, NL; Roman, TS; Drong, AW; Song, C; Gustafsson, S; Day, FR; Esko, T; Fall, T; Kutalik, Z; Luan, J; Randall, JC; Scherag, A; Vedantam, S; Wood, AR; Chen, J; Fehrmann, R; Karjalainen, J; Kahali, B; Liu, CT; Schmidt, EM; Absher, D; Amin, N; Anderson, D; Beekman, M; Bragg-Gresham, JL; Buyske, S; Demirkan, A; Ehret, GB; Feitosa, MF; Goel, A; Jackson, AU; Johnson, T; Kleber, ME; Kristiansson, K; Mangino, M; Leach, IM; Medina-Gomez, C; Palmer, CD; Pasko, D; Pechlivanis, S; Peters, MJ; Prokopenko, I; Stančáková, A; Sung, YJ; Tanaka, T; Teumer, A; Van Vliet-Ostaptchouk, JV; Yengo, L; Zhang, W; Albrecht, E; Ärnlöv, J; Arscott, GM; Bandinelli, S; Barrett, A; Bellis, C; Bennett, AJ; Berne, C; Blüher, M; Böhringer, S; Bonnet, F; Böttcher, Y; Bruinenberg, M; Carba, DB; Caspersen, IH; Clarke, R; Daw, EW; Deelen, J; Deelman, E; Delgado, G; Doney, AS; Eklund, N; Erdos, MR; Estrada, K; Eury, E; Friedrich, N; Garcia, ME; Giedraitis, V; Gigante, B; Go, AS; Golay, A; Grallert, H; Grammer, TB; Gräßler, J; Grewal, J; Groves, CJ; Haller, T; Hallmans, G; Hartman, CA; Hassinen, M; Hayward, C; Heikkilä, K; Herzig, KH; Helmer, Q; Hillege, HL; Holmen, O; Hunt, SC; Isaacs, A; Ittermann, T; James, AL; Johansson, I; Juliusdottir, T; Kalafati, IP; Kinnunen, L; Koenig, W; Kooner, IK; Kratzer, W; Lamina, C; Leander, K; Lee, NR; Lichtner, P; Lind, L; Lindström, J; Lobbens, S; Lorentzon, M; Mach, F; Magnusson, PK; Mahajan, A; McArdle, WL; Menni, C; Merger, S; Mihailov, E; Milani, L; Mills, R; Moayyeri, A; Monda, KL; Mooijaart, SP; Mühleisen, TW; Mulas, A; Müller, G; Müller-Nurasyid, M; Nagaraja, R; Nalls, MA; Narisu, N; Glorioso, N; Nolte, IM; Olden, M; Rayner, NW; Renstrom, F; Ried, JS; Robertson, NR; Rose, LM; Sanna, S; Scharnagl, H; Scholtens, S; Sennblad, B; Seufferlein, T; Sitlani, CM; Smith, AV; Stirrups, K; Stringham, HM; Sundström, J; Swertz, MA; Swift, AJ; Syvänen, AC; Tayo, BO; Thorand, B; Thorleifsson, G; Tomaschitz, A; Troffa, C; van Oort, FV; Verweij, N; Vonk, JM; Waite, LL; Wennauer, R; Wilsgaard, T; Wojczynski, MK; Wong, A; Zhang, Q; Zhao, JH; Brennan, EP; Choi, M; Eriksson, P; Folkersen, L; Franco-Cereceda, A; Gharavi, AG; Hedman, ÅK; Hivert, MF; Huang, J; Kanoni, S; Karpe, F; Keildson, S; Kiryluk, K; Liang, L; Lifton, RP; Ma, B; McKnight, AJ; McPherson, R; Metspalu, A; Min, JL; Moffatt, MF; Montgomery, GW; Murabito, JM; Nicholson, G; Nyholt, DR; Olsson, C; Perry, JR; Reinmaa, E; Salem, RM; Sandholm, N; Schadt, EE; Scott, RA; Stolk, L; Vallejo, EE; Westra, HJ; Zondervan, KT; ADIPOGen Consortium; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GEFOS Consortium; GENIE Consortium; GLGC; ICBP; International Endogene Consortium; LifeLines Cohort Study; MAGIC Investigators; MuTHER Consortium; PAGE Consortium; ReproGen Consortium; Amouyel, P; Arveiler, D; Bakker, SJ; Beilby, J; Bergman, RN; Blangero, J; Brown, MJ; Burnier, M; Campbell, H; Chakravarti, A; Chines, PS; Claudi-Boehm, S; Collins, FS; Crawford, DC; Danesh, J; de Faire, U; de Geus, EJ; Dörr, M; Erbel, R; Eriksson, JG; Farrall, M; Ferrannini, E; Ferrières, J; Forouhi, NG; Forrester, T; Franco, OH; Gansevoort, RT; Gieger, C; Gudnason, V; Haiman, CA; Harris, TB; Hattersley, AT; Heliövaara, M; Hicks, AA; Hingorani, AD; Hoffmann, W; Hofman, A; Homuth, G; Humphries, SE; Hyppönen, E; Illig, T; Jarvelin, MR; Johansen, B; Jousilahti ... New genetic loci link adipose and insulin biology to body fat distribution.
Nature. 2015; 518(7538):187-196 Doi: 10.1038/nature14132 [OPEN ACCESS]
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** Zheng, HF; Forgetta, V; Hsu, YH; Estrada, K; Rosello-Diez, A; Leo, PJ; Dahia, CL; Park-Min, KH; Tobias, JH; Kooperberg, C; Kleinman, A; Styrkarsdottir, U; Liu, CT; Uggla, C; Evans, DS; Nielson, CM; Walter, K; Pettersson-Kymmer, U; McCarthy, S; Eriksson, J; Kwan, T; Jhamai, M; Trajanoska, K; Memari, Y; Min, J; Huang, J; Danecek, P; Wilmot, B; Li, R; Chou, WC; Mokry, LE; Moayyeri, A; Claussnitzer, M; Cheng, CH; Cheung, W; Medina-Gómez, C; Ge, B; Chen, SH; Choi, K; Oei, L; Fraser, J; Kraaij, R; Hibbs, MA; Gregson, CL; Paquette, D; Hofman, A; Wibom, C; Tranah, GJ; Marshall, M; Gardiner, BB; Cremin, K; Auer, P; Hsu, L; Ring, S; Tung, JY; Thorleifsson, G; Enneman, AW; van, Schoor, NM; de, Groot, LC; van, der, Velde, N; Melin, B; Kemp, JP; Christiansen, C; Sayers, A; Zhou, Y; Calderari, S; van, Rooij, J; Carlson, C; Peters, U; Berlivet, S; Dostie, J; Uitterlinden, AG; Williams, SR; Farber, C; Grinberg, D; LaCroix, AZ; Haessler, J; Chasman, DI; Giulianini, F; Rose, LM; Ridker, PM; Eisman, JA; Nguyen, TV; Center, JR; Nogues, X; Garcia-Giralt, N; Launer, LL; Gudnason, V; Mellström, D; Vandenput, L; Amin, N; van, Duijn, CM; Karlsson, MK; Ljunggren, Ö; Svensson, O; Hallmans, G; Rousseau, F; Giroux, S; Bussière, J; Arp, PP; Koromani, F; Prince, RL; Lewis, JR; Langdahl, BL; Hermann, AP; Jensen, JE; Kaptoge, S; Khaw, KT; Reeve, J; Formosa, MM; Xuereb-Anastasi, A; Åkesson, K; McGuigan, FE; Garg, G; Olmos, JM; Zarrabeitia, MT; Riancho, JA; Ralston, SH; Alonso, N; Jiang, X; Goltzman, D; Pastinen, T; Grundberg, E; Gauguier, D; Orwoll, ES; Karasik, D; Davey-Smith, G; Smith, AV; Siggeirsdottir, K; Harris, TB; Zillikens, MC; van, Meurs, JB; Thorsteinsdottir, U; Maurano, MT; Timpson, NJ; Soranzo, N; Durbin, R; Wilson, SG; Ntzani, EE; Brown, MA; Stefansson, K; Hinds, DA; Spector, T; Cupples, LA; Ohlsson, C; Greenwood, CM; Jackson, RD; Rowe, DW; Loomis, CA; Evans, DM; Ackert-Bicknell, CL; Joyner, AL; Duncan, EL; Kiel, DP; Rivadeneira, F; Richards, JB, , AOGC, Consortium;UK10K, Consortium Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature. 2015; 526(7571): 112-7. Doi: 10.1038/nature14878 [OPEN ACCESS]
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2014

Originalarbeit (Zeitschrift)

** Oei, L; Estrada, K; Duncan, EL; Christiansen, C; Liu, CT; Langdahl, BL; Obermayer-Pietsch, B; Riancho, JA; Prince, RL; van, Schoor, NM; McCloskey, E; Hsu, YH; Evangelou, E; Ntzani, E; Evans, DM; Alonso, N; Husted, LB; Valero, C; Hernandez, JL; Lewis, JR; Kaptoge, SK; Zhu, K; Cupples, LA; Medina-Gómez, C; Vandenput, L; Kim, GS; Hun, Lee, S; Castaño-Betancourt, MC; Oei, EH; Martinez, J; Daroszewska, A; van, der, Klift, M; Mellström, D; Herrera, L; Karlsson, MK; Hofman, A; Ljunggren, Ö; Pols, HA; Stolk, L; van, Meurs, JB; Ioannidis, JP; Zillikens, MC; Lips, P; Karasik, D; Uitterlinden, AG; Styrkarsdottir, U; Brown, MA; Koh, JM; Richards, JB; Reeve, J; Ohlsson, C; Ralston, SH; Kiel, DP; Rivadeneira, F Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locus.
Bone. 2014; 59:20-7 Doi: 10.1016/j.bone.2013.10.015 [OPEN ACCESS]
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** Oei, L; Hsu, YH; Styrkarsdottir, U; Eussen, BH; de, Klein, A; Peters, MJ; Halldorsson, B; Liu, CT; Alonso, N; Kaptoge, SK; Thorleifsson, G; Hallmans, G; Hocking, LJ; Husted, LB; Jameson, KA; Kruk, M; Lewis, JR; Patel, MS; Scollen, S; Svensson, O; Trompet, S; van, Schoor, NM; Zhu, K; Buckley, BM; Cooper, C; Ford, I; Goltzman, D; González-Macías, J; Langdahl, BL; Leslie, WD; Lips, P; Lorenc, RS; Olmos, JM; Pettersson-Kymmer, U; Reid, DM; Riancho, JA; Slagboom, PE; Garcia-Ibarbia, C; Ingvarsson, T; Johannsdottir, H; Luben, R; Medina-Gómez, C; Arp, P; Nandakumar, K; Palsson, ST; Sigurdsson, G; van, Meurs, JB; Zhou, Y; Hofman, A; Jukema, JW; Pols, HA; Prince, RL; Cupples, LA; Marshall, CR; Pinto, D; Sato, D; Scherer, SW; Reeve, J; Thorsteinsdottir, U; Karasik, D; Richards, JB; Stefansson, K; Uitterlinden, AG; Ralston, SH; Ioannidis, JP; Kiel, DP; Rivadeneira, F; Estrada, K A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.
J Med Genet. 2014; 51(2): 122-31. Doi: 10.1136/jmedgenet-2013-102064
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Übersichtsarbeit

** Alonso, N; Ralston, SH Unveiling the mysteries of the genetics of osteoporosis.
J Endocrinol Invest. 2014; 37(10): 925-34. Doi: 10.1007/s40618-014-0149-7
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2013

Originalarbeit (Zeitschrift)

** Albagha, OM; Visconti, MR; Alonso, N; Wani, S; Goodman, K; Fraser, WD; Gennari, L; Merlotti, D; Gianfrancesco, F; Esposito, T; Rendina, D; di, Stefano, M; Isaia, G; Brandi, ML; Giusti, F; Del, Pino-Montes, J; Corral-Gudino, L; Gonzalez-Sarmiento, R; Ward, L; Rea, SL; Ratajczak, T; Walsh, JP; Ralston, SH Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
J Bone Miner Res. 2013; 28(11): 2338-46. Doi: 10.1002/jbmr.1975
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2012

Originalarbeit (Zeitschrift)

** Estrada, K; Styrkarsdottir, U; Evangelou, E; Hsu, YH; Duncan, EL; Ntzani, EE; Oei, L; Albagha, OM; Amin, N; Kemp, JP; Koller, DL; Li, G; Liu, CT; Minster, RL; Moayyeri, A; Vandenput, L; Willner, D; Xiao, SM; Yerges-Armstrong, LM; Zheng, HF; Alonso, N; Eriksson, J; Kammerer, CM; Kaptoge, SK; Leo, PJ; Thorleifsson, G; Wilson, SG; Wilson, JF; Aalto, V; Alen, M; Aragaki, AK; Aspelund, T; Center, JR; Dailiana, Z; Duggan, DJ; Garcia, M; Garcia-Giralt, N; Giroux, S; Hallmans, G; Hocking, LJ; Husted, LB; Jameson, KA; Khusainova, R; Kim, GS; Kooperberg, C; Koromila, T; Kruk, M; Laaksonen, M; Lacroix, AZ; Lee, SH; Leung, PC; Lewis, JR; Masi, L; Mencej-Bedrac, S; Nguyen, TV; Nogues, X; Patel, MS; Prezelj, J; Rose, LM; Scollen, S; Siggeirsdottir, K; Smith, AV; Svensson, O; Trompet, S; Trummer, O; van, Schoor, NM; Woo, J; Zhu, K; Balcells, S; Brandi, ML; Buckley, BM; Cheng, S; Christiansen, C; Cooper, C; Dedoussis, G; Ford, I; Frost, M; Goltzman, D; González-Macías, J; Kähönen, M; Karlsson, M; Khusnutdinova, E; Koh, JM; Kollia, P; Langdahl, BL; Leslie, WD; Lips, P; Ljunggren, Ö; Lorenc, RS; Marc, J; Mellström, D; Obermayer-Pietsch, B; Olmos, JM; Pettersson-Kymmer, U; Reid, DM; Riancho, JA; Ridker, PM; Rousseau, F; Slagboom, PE; Tang, NL; Urreizti, R; Van, Hul, W; Viikari, J; Zarrabeitia, MT; Aulchenko, YS; Castano-Betancourt, M; Grundberg, E; Herrera, L; Ingvarsson, T; Johannsdottir, H; Kwan, T; Li, R; Luben, R; Medina-Gómez, C; Palsson, ST; Reppe, S; Rotter, JI; Sigurdsson, G; van, Meurs, JB; Verlaan, D; Williams, FM; Wood, AR; Zhou, Y; Gautvik, KM; Pastinen, T; Raychaudhuri, S; Cauley, JA; Chasman, DI; Clark, GR; Cummings, SR; Danoy, P; Dennison, EM; Eastell, R; Eisman, JA; Gudnason, V; Hofman, A; Jackson, RD; Jones, G; Jukema, JW; Khaw, KT; Lehtimäki, T; Liu, Y; Lorentzon, M; McCloskey, E; Mitchell, BD; Nandakumar, K; Nicholson, GC; Oostra, BA; Peacock, M; Pols, HA; Prince, RL; Raitakari, O; Reid, IR; Robbins, J; Sambrook, PN; Sham, PC; Shuldiner, AR; Tylavsky, FA; van, Duijn, CM; Wareham, NJ; Cupples, LA; Econs, MJ; Evans, DM; Harris, TB; Kung, AW; Psaty, BM; Reeve, J; Spector, TD; Streeten, EA; Zillikens, MC; Thorsteinsdottir, U; Ohlsson, C; Karasik, D; Richards, JB; Brown, MA; Stefansson, K; Uitterlinden, AG; Ralston, SH; Ioannidis, JP; Kiel, DP; Rivadeneira, F Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
NAT GENET. 2012; 44(5): 491-501. Doi: 10.1038/ng.2249 [OPEN ACCESS]
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** Liu, CT; Estrada, K; Yerges-Armstrong, LM; Amin, N; Evangelou, E; Li, G; Minster, RL; Carless, MA; Kammerer, CM; Oei, L; Zhou, Y; Alonso, N; Dailiana, Z; Eriksson, J; García-Giralt, N; Giroux, S; Husted, LB; Khusainova, RI; Koromila, T; Kung, AW; Lewis, JR; Masi, L; Mencej-Bedrac, S; Nogues, X; Patel, MS; Prezelj, J; Richards, JB; Sham, PC; Spector, T; Vandenput, L; Xiao, SM; Zheng, HF; Zhu, K; Balcells, S; Brandi, ML; Frost, M; Goltzman, D; González-Macías, J; Karlsson, M; Khusnutdinova, EK; Kollia, P; Langdahl, BL; Ljunggren, O; Lorentzon, M; Marc, J; Mellström, D; Ohlsson, C; Olmos, JM; Ralston, SH; Riancho, JA; Rousseau, F; Urreizti, R; Van, Hul, W; Zarrabeitia, MT; Castano-Betancourt, M; Demissie, S; Grundberg, E; Herrera, L; Kwan, T; Medina-Gómez, C; Pastinen, T; Sigurdsson, G; Thorleifsson, G; Vanmeurs, JB; Blangero, J; Hofman, A; Liu, Y; Mitchell, BD; O'Connell, JR; Oostra, BA; Rotter, JI; Stefansson, K; Streeten, EA; Styrkarsdottir, U; Thorsteinsdottir, U; Tylavsky, FA; Uitterlinden, A; Cauley, JA; Harris, TB; Ioannidis, JP; Psaty, BM; Robbins, JA; Zillikens, MC; Vanduijn, CM; Prince, RL; Karasik, D; Rivadeneira, F; Kiel, DP; Cupples, LA; Hsu, YH Assessment of gene-by-sex interaction effect on bone mineral density.
J Bone Miner Res. 2012; 27(10): 2051-64. Doi: 10.1002/jbmr.1679 [OPEN ACCESS]
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2011

Originalarbeit (Zeitschrift)

** Albagha, OM; Wani, SE; Visconti, MR; Alonso, N; Goodman, K; Brandi, ML; Cundy, T; Chung, PY; Dargie, R; Devogelaer, JP; Falchetti, A; Fraser, WD; Gennari, L; Gianfrancesco, F; Hooper, MJ; Van, Hul, W; Isaia, G; Nicholson, GC; Nuti, R; Papapoulos, S; Montes, Jdel, P; Ratajczak, T; Rea, SL; Rendina, D; Gonzalez-Sarmiento, R; Di, Stefano, M; Ward, LC; Walsh, JP; Ralston, SH, , Genetic, Determinants, of, Paget's, Disease, (GDPD), Consortium Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Nat Genet. 2011; 43(7): 685-9. Doi: 10.1038/ng.845
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2010

Originalarbeit (Zeitschrift)

** Albagha, OM; Visconti, MR; Alonso, N; Langston, AL; Cundy, T; Dargie, R; Dunlop, MG; Fraser, WD; Hooper, MJ; Isaia, G; Nicholson, GC; del, Pino, Montes, J; Gonzalez-Sarmiento, R; di, Stefano, M; Tenesa, A; Walsh, JP; Ralston, SH Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Nat Genet. 2010; 42(6): 520-4. Doi: 10.1038/ng.562 [OPEN ACCESS]
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** Visconti, MR; Langston, AL; Alonso, N; Goodman, K; Selby, PL; Fraser, WD; Ralston, SH Mutations of SQSTM1 are associated with severity and clinical outcome in paget disease of bone.
J Bone Miner Res. 2010; 25(11): 2368-73. Doi: 10.1002/jbmr.132
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