Anders Kämpe

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Postmenopausal Women

Genome Wide Association

Top Venues

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Molecular psychiatry

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Anders Kämpe, Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola-Olli, Lea Urpa, Willehard Haaki, Jarmo Hietala, Erkki Isometsä, Tuomas Jukuri, Olli Kampman, Tuula Kieseppä, Kaisla Lahdensuo, Jouko Lönnqvist, Teemu Männynsalo, Tiina Paunio, Jussi Niemi-Pynttäri, Kimmo Suokas, Annamari Tuulio-Henriksson, Juha Veijola, Asko Wegelius, null null, Mark Daly, Jacob Taylor, Kenneth S Kendler, Aarno Palotie, Olli Pietiläinen
Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders. Molecular psychiatry (2024)
Anders Kämpe, Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola-Olli, Lea Urpa, Willehard Haaki, Jarmo Hietala, Erkki Isometsä, Tuomas Jukuri, Olli Kampman, Tuula Kieseppä, Kaisla Lahdensuo, Jouko Lönnqvist, Teemu Männynsalo, Tiina Paunio, Jussi Niemi-Pynttäri, Kimmo Suokas, Annamari Tuulio-Henriksson, Juha Veijola, Asko Wegelius, null null, Mark Daly, Jacob Taylor, Kenneth S Kendler, Aarno Palotie, Olli Pietiläinen
Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders. Molecular psychiatry (2024)
Maria Nethander, Sofia Movérare-Skrtic, Anders Kämpe, Eivind Coward, Ene Reimann, Louise Grahnemo, Éva Borbély, Zsuzsanna Helyes, Thomas Funck-Brentano, Martine Cohen Solal, Juha Tuukkanen, Antti Koskela, Jianyao Wu, Lei Li, Tianyuan Lu, Maiken E Gabrielsen, null null, Reedik Mägi, Mari Hoff, Ulf H Lerner, Petra Henning, Henrik Ullum, Christian Erikstrup, Soren Brunak, null null, Arnulf Langhammer, Tiinamaija Tuomi, Asmundur Oddsson, Kari Stefansson, Ulrika Pettersson-Kymmer, Sisse Rye Ostrowski, Ole Birger Vesterager Pedersen, Unnur Styrkarsdottir, Outimaija Mäkitie, Kristian Hveem, John Brent Richards, Claes Ohlsson
An atlas of genetic determinants of forearm fracture. Nature genetics (2023)
Riikka E Makitie, Petra Henning, Yaming Jiu, Anders Kämpe, Konstantin Kogan, Alice Costantini, Ville-Valtteri Välimäki, Carolina Medina-Gomez, Minna Pekkinen, Isidro B Salusky, Camilla Schalin-Jäntti, Maria K Haanpää, Fernando Rivadeneira, John H Duncan Bassett, Graham R Williams, Ulf H Lerner, Renata C Pereira, Pekka Lappalainen, Outimaija Mäkitie
An ARHGAP25 variant links aberrant Rac1 function to early-onset skeletal fragility. JBMR plus 5 (7) (2021)
Riikka E Makitie, Matthias Hackl, Moritz Weigl, Amelie Frischer, Anders Kämpe, Alice Costantini, Johannes Grillari, Outimaija Mäkitie
Unique, Gender-Dependent Serum microRNA Profile in PLS3 Gene-Related Osteoporosis. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 35 (10) (2020)
Despoina Manousaki, Anders Kämpe, Vincenzo Forgetta, Riikka E Makitie, Ghalib Bardai, Alexandre Belisle, Rui Li, Sture Andersson, Outimaija Mäkitie, Frank Rauch, John Brent Richards
Increased Burden of Common Risk Alleles in Children With a Significant Fracture History. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 35 (5) (2020)
Riikka E Makitie, Anders Kämpe, Alice Costantini, Jessica J Alm, Per Magnusson, Outimaija Mäkitie
Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 35 (5) (2020)
Anders Kämpe, Maria Enlund-Cerullo, Saara Valkama, Elisa Holmlund-Suila, Jenni Rosendahl, Helena Henrietta Hauta-Alus, Minna Pekkinen, Sture Andersson, Outimaija Mäkitie
Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. PLoS genetics 15 (12) (2019)