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Page 1
Whole Exome Sequencing in Two Southeast Asian Families With Atypical Femur Fractures.
Zhou W, Nguyen HH, van de Laarschot DM, Howe TS, Koh JSB, Milat F, van Rooij JGJ, Verlouw JAM, van der Eerden BCJ, Stevenson M, Thakker RV, Zillikens MC, Ebeling PR. Zhou W, et al. Among authors: van rooij jgj. JBMR Plus. 2022 Jul 3;6(8):e10659. doi: 10.1002/jbm4.10659. eCollection 2022 Aug. JBMR Plus. 2022. PMID: 35991532 Free PMC article.
Proteomics of the dentate gyrus reveals semantic dementia specific molecular pathology.
Mol MO, Miedema SSM, Melhem S, Li KW, Koopmans F, Seelaar H, Gottmann K, Lessmann V, Bank NB, Smit AB, van Swieten JC, van Rooij JGJ. Mol MO, et al. Among authors: van rooij jgj. Acta Neuropathol Commun. 2022 Dec 28;10(1):190. doi: 10.1186/s40478-022-01499-1. Acta Neuropathol Commun. 2022. PMID: 36578035 Free PMC article.
Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane.
Corominas J, Colijn JM, Geerlings MJ, Pauper M, Bakker B, Amin N, Lores Motta L, Kersten E, Garanto A, Verlouw JAM, van Rooij JGJ, Kraaij R, de Jong PTVM, Hofman A, Vingerling JR, Schick T, Fauser S, de Jong EK, van Duijn CM, Hoyng CB, Klaver CCW, den Hollander AI. Corominas J, et al. Among authors: van duijn cm, van rooij jgj. Ophthalmology. 2018 Sep;125(9):1433-1443. doi: 10.1016/j.ophtha.2018.03.040. Epub 2018 Apr 26. Ophthalmology. 2018. PMID: 29706360 Free PMC article.
The Genetics of Atypical Femur Fractures-a Systematic Review.
Zhou W, van Rooij JGJ, Ebeling PR, Verkerk AJMH, Zillikens MC. Zhou W, et al. Among authors: van rooij jgj. Curr Osteoporos Rep. 2021 Apr;19(2):123-130. doi: 10.1007/s11914-021-00658-y. Epub 2021 Feb 15. Curr Osteoporos Rep. 2021. PMID: 33587247 Free PMC article.
Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness.
Vojinovic D, Kavousi M, Ghanbari M, Brouwer RWW, van Rooij JGJ, van den Hout MCGN, Kraaij R, van Ijcken WFJ, Uitterlinden AG, van Duijn CM, Amin N. Vojinovic D, et al. Among authors: van duijn cm, van ijcken wfj, van rooij jgj, van den hout mcgn. Front Genet. 2018 Oct 9;9:420. doi: 10.3389/fgene.2018.00420. eCollection 2018. Front Genet. 2018. PMID: 30356672 Free PMC article.
Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length.
van der Spek A, Warner SC, Broer L, Nelson CP, Vojinovic D, Ahmad S, Arp PP, Brouwer RWW, Denniff M, van den Hout MCGN, van Rooij JGJ, Kraaij R, van IJcken WFJ, Samani NJ, Ikram MA, Uitterlinden AG, Codd V, Amin N, van Duijn CM. van der Spek A, et al. Among authors: van duijn cm, van ijcken wfj, van rooij jgj, van den hout mcgn. Front Genet. 2020 Apr 30;11:337. doi: 10.3389/fgene.2020.00337. eCollection 2020. Front Genet. 2020. PMID: 32425970 Free PMC article.
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Pankratz N, Wei P, Brody JA, Chen MH, de Vries PS, Huffman JE, Stimson MR, Auer PL, Boerwinkle E, Cushman M, de Maat MPM, Folsom AR, Franco OH, Gibbs RA, Haagenson KK, Hofman A, Johnsen JM, Kovar CL, Kraaij R, McKnight B, Metcalf GA, Muzny D, Psaty BM, Tang W, Uitterlinden AG, van Rooij JGJ, Dehghan A, O'Donnell CJ, Reiner AP, Morrison AC, Smith NL. Pankratz N, et al. Among authors: van rooij jgj. Hum Mol Genet. 2022 Sep 10;31(18):3120-3132. doi: 10.1093/hmg/ddac100. Hum Mol Genet. 2022. PMID: 35552711 Free PMC article.
Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients.
Mol MO, van Rooij JGJ, Wong TH, Melhem S, Verkerk AJMH, Kievit AJA, van Minkelen R, Rademakers R, Pottier C, Kaat LD, Seelaar H, van Swieten JC, Dopper EGP. Mol MO, et al. Among authors: van minkelen r, van swieten jc, van rooij jgj. Neurobiol Aging. 2021 Jan;97:148.e9-148.e16. doi: 10.1016/j.neurobiolaging.2020.07.014. Epub 2020 Jul 30. Neurobiol Aging. 2021. PMID: 32843152 Free article.
45 results