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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 The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease : evidence from cross-sectional, longitudinal and Mendelian randomisation analyses
Drake, Isabel ^LU ; Fryk, Emanuel ; Strindberg, Lena ; Lundqvist, Annika ; Rosengren, Anders H. ^LU ; Groop, Leif ^LU ; Ahlqvist, Emma ^LU ; Borén, Jan ; Orho-Melander, Marju ^LU and Jansson, Per Anders (2022) In Diabetologia 65(1). p.128-139
- Contribution to journal › Article
2021
Mark Elevated circulating follistatin associates with an increased risk of type 2 diabetes
Wu, Chuanyan ^LU ; Borné, Yan ^LU ; Gao, Rui ; López Rodriguez, Maykel ; Roell, William C ; Wilson, Jonathan M ; Regmi, Ajit ; Luan, Cheng ^LU ; Aly, Dina Mansour ^LU and Peter, Andreas , et al. (2021) In Nature Communications 12. p.1-10
- Contribution to journal › Article
2020
Mark Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease
Luukkonen, Panu K. ; Tukiainen, Taru ; Juuti, Anne ; Sammalkorpi, Henna ; Nidhina Haridas, P. A. ; Niemelä, Onni ; Arola, Johanna ; Orho-Melander, Marju ^LU ; Hakkarainen, Antti and Kovanen, Petri T. , et al. (2020) In JCI Insight 5(5).
- Contribution to journal › Article
Mark Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran, Praveen ; Fava, Cristiano ^LU ; Melander, Olle ^LU ; Orho-Melander, Marju ^LU ; Poveda, Alaitz ^LU ; V. Varga, Tibor ^LU ; Renström, Frida ^LU ; Franks, Paul ^LU ; Tuomi, Tiinamaija ^LU and Almgren, Peter ^LU , et al. (2020) In Nature Genetics 52(12). p.1314-1332
- Contribution to journal › Article
2019
Mark A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
Ahluwalia, Tarunveer S. ; Schulz, Christina Alexandra ^LU ; Waage, Johannes ; Skaaby, Tea ; Sandholm, Niina ; van Zuydam, Natalie ; Charmet, Romain ; Bork-Jensen, Jette ; Almgren, Peter ^LU and Thuesen, Betina H. , et al. (2019) In Diabetologia 62(2). p.292-305
- Contribution to journal › Article
Mark Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
Arora, Geeti P ^LU ; Åkerlund, Mikael ^LU ; Brøns, Charlotte ; Moen, Gunn-Helen ; Wasenius, Niko S ; Sommer, Christine ; Jenum, Anne K ; Almgren, Peter ^LU ; Thaman, Richa G and Orho-Melander, Marju ^LU , et al. (2019) In Journal of Internal Medicine 286(2). p.192-206
- Contribution to journal › Article
2018
Mark Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Gusarova, Viktoria ; O'Dushlaine, Colm ; Teslovich, Tanya M ; Benotti, Peter N ; Mirshahi, Tooraj ; Gottesman, Omri ; Van Hout, Cristopher V ; Murray, Michael F ; Mahajan, Anubha and Nielsen, Jonas B , et al. (2018) In Nature Communications 9. p.1-11
- Contribution to journal › Article
Mark A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam, Natalie R ; Ahlqvist, Emma ^LU ; Ladenvall, Claes ^LU ; Almgren, Peter ^LU ; Schulz, Christina-Alexandra ^LU ; Orho-Melander, Marju ^LU ; Melander, Olle ^LU ; Lyssenko, Valeriya ^LU ; Tuomi, Tiinamaija ^LU and Groop, Leif C ^LU , et al. (2018) In Diabetes 67(7). p.1414-1427
- Contribution to journal › Article
Mark Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
Mahajan, Anubha ; Wessel, Jennifer ; Willems, Sara M ; Zhao, Wei ; Robertson, Neil R ; Chu, Audrey Y. ; Kravic, Jasmina ^LU ; Ahlqvist, Emma ^LU ; Rosengren, Anders ^LU and Groop, Leif ^LU , et al. (2018) In Nature Genetics 50(4). p.559-571
- Contribution to journal › Article

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