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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
2001 2
2005 1
2006 2
2007 1
2008 4
2010 3
2012 1
2013 2
2014 3
2015 2
2016 3
2017 3
2019 3
2020 2
2021 2
2022 2
2023 1
2024 1

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33 results

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Page 1
DNA methylation episignature in Gabriele-de Vries syndrome.
Cherik F, Reilly J, Kerkhof J, Levy M, McConkey H, Barat-Houari M, Butler KM, Coubes C, Lee JA, Le Guyader G, Louie RJ, Patterson WG, Tedder ML, Bak M, Hammer TB, Craigen W, Démurger F, Dubourg C, Fradin M, Franciskovich R, Frengen E, Friedman J, Palares NR, Iascone M, Misceo D, Monin P, Odent S, Philippe C, Rouxel F, Saletti V, Strømme P, Thulin PC, Sadikovic B, Genevieve D. Cherik F, et al. Among authors: thulin pc. Genet Med. 2022 Apr;24(4):905-914. doi: 10.1016/j.gim.2021.12.003. Epub 2022 Jan 10. Genet Med. 2022. PMID: 35027293 Free article.
Exocrine pancreatic function is preserved in systemic sclerosis.
Bozovic G, Pullerits R, Ståhl A, Ydström K, Wenger D, Marsal J, Thulin P, Andréasson K. Bozovic G, et al. Among authors: thulin p. Arthritis Res Ther. 2019 Feb 12;21(1):52. doi: 10.1186/s13075-019-1840-z. Arthritis Res Ther. 2019. PMID: 30755261 Free PMC article.
The regulatory role of PGC1α-related coactivator in response to drug-induced liver injury.
Buler M, Naessens T, Mattsson J, Morias Y, Söderberg M, Robbins P, Kärrberg L, Svensson TS, Thulin P, Glinghammar B, Scarpulla RC, Andersson U. Buler M, et al. Among authors: thulin p. FASEB Bioadv. 2020 Jul 11;2(8):453-463. doi: 10.1096/fba.2020-00003. eCollection 2020 Aug. FASEB Bioadv. 2020. PMID: 32821877 Free PMC article.
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.
Gabriele M, Vulto-van Silfhout AT, Germain PL, Vitriolo A, Kumar R, Douglas E, Haan E, Kosaki K, Takenouchi T, Rauch A, Steindl K, Frengen E, Misceo D, Pedurupillay CRJ, Stromme P, Rosenfeld JA, Shao Y, Craigen WJ, Schaaf CP, Rodriguez-Buritica D, Farach L, Friedman J, Thulin P, McLean SD, Nugent KM, Morton J, Nicholl J, Andrieux J, Stray-Pedersen A, Chambon P, Patrier S, Lynch SA, Kjaergaard S, Tørring PM, Brasch-Andersen C, Ronan A, van Haeringen A, Anderson PJ, Powis Z, Brunner HG, Pfundt R, Schuurs-Hoeijmakers JHM, van Bon BWM, Lelieveld S, Gilissen C, Nillesen WM, Vissers LELM, Gecz J, Koolen DA, Testa G, de Vries BBA. Gabriele M, et al. Among authors: thulin p. Am J Hum Genet. 2017 Jun 1;100(6):907-925. doi: 10.1016/j.ajhg.2017.05.006. Am J Hum Genet. 2017. PMID: 28575647 Free PMC article.
33 results