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Search: (WFRF:(Strawbridge RJ)) pers:(Silveira A) > (2015-2019) > Rare and low-freque...

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

Huffman, JE (author)
de Vries, PS (author)
Morrison, AC (author)
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Sabater-Lleal, M (author)
Karolinska Institutet
Kacprowski, T (author)
Auer, PL (author)
Brody, JA (author)
Chasman, DI (author)
Chen, MH (author)
Guo, XQ (author)
Lin, LA (author)
Marioni, RE (author)
Muller-Nurasyid, M (author)
Yanek, LR (author)
Pankratz, N (author)
Grove, ML (author)
de Maat, MPM (author)
Cushman, M (author)
Wiggins, KL (author)
Qi, LH (author)
Sennblad, B (author)
Karolinska Institutet
Harris, SE (author)
Polasek, O (author)
Riess, H (author)
Rivadeneira, F (author)
Rose, LM (author)
Goel, A (author)
Taylor, KD (author)
Teumer, A (author)
Uitterlinden, AG (author)
Vaidya, D (author)
Yao, J (author)
Tang, WH (author)
Levy, D (author)
Waldenberger, M (author)
Becker, DM (author)
Folsom, AR (author)
Giulianini, F (author)
Greinacher, A (author)
Hofman, A (author)
Huang, CC (author)
Kooperberg, C (author)
Silveira, A (author)
Karolinska Institutet
Starr, JM (author)
Strauch, K (author)
Strawbridge, RJ (author)
Karolinska Institutet
Wright, AF (author)
McKnight, B (author)
Franco, OH (author)
Zakai, N (author)
Mathias, RA (author)
Psaty, BM (author)
Ridker, PM (author)
Tofler, GH (author)
Volker, U (author)
Watkins, H (author)
Fornage, M (author)
Hamsten, A (author)
Karolinska Institutet
Deary, IJ (author)
Boerwinkle, E (author)
Koenig, W (author)
Rotter, JI (author)
Hayward, C (author)
Dehghan, A (author)
Reiner, AP (author)
O'Donnell, CJ (author)
Smith, NL (author)
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 (creator_code:org_t)
American Society of Hematology, 2015
2015
English.
In: Blood. - : American Society of Hematology. - 1528-0020 .- 0006-4971. ; 126:11, s. E19-E29
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Twelve independent, novel, low-frequency (n = 2) and rare (n = 10) genetic variants were associated with fibrinogen, FVII, FVIII, or vWF. Nine were within previously associated genes, and 3 novel candidate genes (KCNT1, HID1, and KATNB1) were confined to cohorts of African ancestry.

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