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2025
Mark Fine-mapping in admixed populations using CARMA-X, with applications to Latin American studies
Yang, Zikun ; Wang, Chen ; Posadas-Garcia, Yuridia Selene ; Añorve-Garibay, Valeria ; Vardarajan, Badri ; Estrada, Andrés Moreno ; Sohail, Mashaal ; Mayeux, Richard and Ionita-Laza, Iuliana ^LU (2025) In American Journal of Human Genetics 112(5). p.1215-1232
- Contribution to journal › Article
2024
Mark Local genetic correlation via knockoffs reduces confounding due to cross-trait assortative mating
Ma, Shiyang ; Wang, Fan ; Border, Richard ; Buxbaum, Joseph ; Zaitlen, Noah and Ionita-Laza, Iuliana ^LU (2024) In American Journal of Human Genetics 111(12). p.2839-2848
- Contribution to journal › Article
Mark KnockoffHybrid : A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies
Yang, Yi ; Wang, Qi ; Wang, Chen ; Buxbaum, Joseph and Ionita-Laza, Iuliana ^LU (2024) In American Journal of Human Genetics 111(7). p.1448-1461
- Contribution to journal › Article
Mark Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
Dareng, E.O. ; Olsson, H. ^LU and Gayther, S.A. (2024) In American Journal of Human Genetics 111(6). p.1061-1083
- Contribution to journal › Article
Mark Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Manzoni, Claudia ; Kia, Demis A. ; Ferrari, Raffaele ; Leonenko, Ganna ; Costa, Beatrice ; Saba, Valentina ^LU ; Jabbari, Edwin ; Tan, Manuela MX ; Albani, Diego and Alvarez, Victoria , et al. (2024) In American Journal of Human Genetics 111(7). p.1316-1329
- Contribution to journal › Article
Mark Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
Wallenius, Joel ^LU ; Kafantari, Efthymia ^LU ; Jhaveri, Emma ; Gorcenco, Sorina ^LU ; Ameur, Adam ; Karremo, Christin ^LU ; Dobloug, Sigurd ^LU ; Karrman, Kristina ^LU ; de Koning, Tom ^LU and Ilinca, Andreea ^LU , et al. (2024) In American Journal of Human Genetics 111(1). p.82-95
- Contribution to journal › Article
2022
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
Mark A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
Ramdas, S. ; Poveda, A. ^LU ; Kurbasic, A. ^LU ; Lyssenko, V. ^LU ; Franks, P.W. ^LU and Brown, Christopher D. (2022) In American Journal of Human Genetics 109(8). p.1366-1387
- Contribution to journal › Article
Mark EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis
Adamo, Christin S. ; Beyens, Aude ; Schiavinato, Alvise ; Keene, Douglas R. ; Tufa, Sara F. ; Mörgelin, Matthias ^LU ; Brinckmann, Jürgen ; Sasaki, Takako ; Niehoff, Anja and Dreiner, Maren , et al. (2022) In American Journal of Human Genetics 109(12). p.2230-2252
- Contribution to journal › Article
2021
Mark Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Baxter, J.S. ; Augustinsson, Annelie ^LU ; Olsson, Håkan ^LU and Fletcher, O. (2021) In American Journal of Human Genetics 108(7). p.1190-1203
- Contribution to journal › Article

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