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- 2022
-
Mark
An annotated high-content fluorescence microscopy dataset with Hoechst 33342-stained nuclei and manually labelled outlines : Dataset record
Arvidsson, Malou ; Kazemi Rashed, Salma LU and Aits, Sonja LU
(2022)
- Other contribution › Miscellaneous
-
Mark
Superficial CD34-Positive Fibroblastic Tumor : A Clinicopathologic, Immunohistochemical, and Molecular Study of 59 Cases
- Contribution to journal › Article
-
Mark
A saturated map of common genetic variants associated with human height
Yengo, L. ; Hindy, G. LU ; Kurbasic, A. LU ; Lyssenko, V. LU ; Poveda, A. LU
; Elmståhl, S.
LU
; Franks, P.W.
LU
; Smith, J. Gustav
LU
; Tuomi, T.
LU
and Consortium, The PRACTICAL
, et al.
(2022)
In Nature
p.704-712
- Contribution to journal › Article
-
Mark
Stroke genetics informs drug discovery and risk prediction across ancestries
- Contribution to journal › Article
-
Mark
Iam hiQ-a novel pair of accuracy indices for imputed genotypes
- Contribution to journal › Article
-
Mark
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Aragam, Krishna G ; Hindy, George LU ; Koyama, Satoshi LU
; Melander, Olle
LU
; Orho-Melander, Marju
LU
and Butterworth, Adam S.
(2022)
In Nature Genetics
54(12).
p.1803-1815
- Contribution to journal › Article
-
Mark
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
Manderstedt, E. ; Elf, J. LU ; Svensson, P.J. LU ; Engström, G. LU ; Melander, O. LU
and Zöller, B.
LU
(2022)
In Research and practice in thrombosis and haemostasis
6(7).
- Contribution to journal › Letter
-
Mark
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
- Contribution to journal › Article
-
Mark
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke
Jaworek, T. ; Durda, J.P. ; Engstrom, G. LU ; Ilinca, A. LU
; Smith, Jennifer A.
; Söderholm, M.
LU
; Weir, D.R.
; Lindgren, Arne G.
LU
and Kittner, S.J.
(2022)
In Neurology
99(16).
p.1738-1754
- Contribution to journal › Article
-
Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
Hindy, George LU ; Groop, Leif LU ; Lyssenko, Valeriya LU ; Melander, Olle LU
; Nilsson, Peter M
LU
; Orho-Melander, Marju
LU
and Peloso, Gina M.
(2022)
In American Journal of Human Genetics
109(1).
p.81-96
- Contribution to journal › Article