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

Year Number of Results
1953 1
1981 2
1982 3
1985 3
1986 2
1987 1
1988 1
1993 2
1995 2
1998 1
1999 1
2000 1
2005 2
2007 1
2008 1
2009 1
2010 2
2011 3
2014 2
2015 3
2016 1
2019 2
2020 1
2022 1
2025 0

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40 results

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Page 1
Genetic variants associated with Lp(a) lipoprotein level and coronary disease.
Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, Parish S, Barlera S, Franzosi MG, Rust S, Bennett D, Silveira A, Malarstig A, Green FR, Lathrop M, Gigante B, Leander K, de Faire U, Seedorf U, Hamsten A, Collins R, Watkins H, Farrall M; PROCARDIS Consortium. Clarke R, et al. N Engl J Med. 2009 Dec 24;361(26):2518-28. doi: 10.1056/NEJMoa0902604. N Engl J Med. 2009. PMID: 20032323 Free article.
Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2.
Pott J, Gådin JR, Theusch E, Kleber ME, Delgado GE, Kirsten H, Hauck SM, Burkhardt R, Scharnagl H, Krauss RM, Loeffler M, März W, Thiery J, Silveira A, Van't Hooft FM, Scholz M. Pott J, et al. Hum Mol Genet. 2022 Mar 21;31(6):999-1011. doi: 10.1093/hmg/ddab279. Hum Mol Genet. 2022. PMID: 34590679 Free PMC article.
Relapsing polychondritis mimicking rheumatoid arthritis.
Schlapbach P, Gerber NJ, Ramser P, van't Hooft FM. Schlapbach P, et al. Ann Rheum Dis. 1988 Dec;47(12):1021-6. doi: 10.1136/ard.47.12.1021. Ann Rheum Dis. 1988. PMID: 3207384 Free PMC article.
Pathological laughing.
SILLEVIS SMITT WG, VAN'T HOOFT F. SILLEVIS SMITT WG, et al. Folia Psychiatr Neurol Neurochir Neerl. 1953 Oct;56(5):885-99. Folia Psychiatr Neurol Neurochir Neerl. 1953. PMID: 13117156 No abstract available.
PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease Risk.
Guardiola M, Exeter HJ, Perret C, Folkersen L, Van't Hooft F, Eriksson P, Franco-Cereceda A, Paulsson-Berne G, Palmen J, Li K, Cooper JA, Khaw KT, Mallat Z, Ninio E, Karabina SA, Humphries SE, Boekholdt SM, Holmes MV, Talmud PJ. Guardiola M, et al. Circ Cardiovasc Genet. 2015 Apr;8(2):356-62. doi: 10.1161/CIRCGENETICS.114.000633. Epub 2015 Jan 12. Circ Cardiovasc Genet. 2015. PMID: 25583995 Clinical Trial.
Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition.
Brumpton BM, Fritsche LG, Zheng J, Nielsen JB, Mannila M, Surakka I, Rasheed H, Vie GÅ, Graham SE, Gabrielsen ME, Laugsand LE, Aukrust P, Vatten LJ, Damås JK, Ueland T, Janszky I, Zwart JA, Van't Hooft FM, Seidah NG, Hveem K, Willer C, Smith GD, Åsvold BO; INVENT Consortium. Brumpton BM, et al. Circ Genom Precis Med. 2019 Jan;12(1):e002335. doi: 10.1161/CIRCGEN.118.002335. Circ Genom Precis Med. 2019. PMID: 30645169 Free PMC article. No abstract available.
40 results