Martin Schalling
Martin Schalling
professor i medicinsk genetik, Karolinska Institutet
Verified email at - Homepage
Cited by
Cited by
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Cross-Disorder Group of the Psychiatric Genomics Consortium
The Lancet 381 (9875), 1371-1379, 2013
Somatic mutations of calreticulin in myeloproliferative neoplasms
T Klampfl, H Gisslinger, AS Harutyunyan, H Nivarthi, E Rumi, JD Milosevic, ...
New England Journal of Medicine 369 (25), 2379-2390, 2013
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ...
Nature 478 (7367), 103-109, 2011
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis
H Boström, K Willetts, M Pekny, P Levéen, P Lindahl, H Hedstrand, ...
Cell 85 (6), 863-873, 1996
Overexpression of the obese (ob) gene in adipose tissue of human obese subjects
F Lönnqvist, P Arner, L Nordfors, M Schalling
Nature medicine 1 (9), 950-953, 1995
The neuropeptide Y/agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice
C Broberger, J Johansen, C Johansson, M Schalling, T Hökfelt
Proceedings of the National Academy of Sciences 95 (25), 15043-15048, 1998
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
N Mullins, AJ Forstner, KS O’Connell, B Coombes, JRI Coleman, Z Qiao, ...
Nature genetics 53 (6), 817-829, 2021
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Foci of trinucleotide repeat tanscripts in nuclei of DM cells and tissues
KL Taneja, M McCurrach, M Schalling, D Housman, R Singer
J Cell Bio11995 128, 995-1002, 1995
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2
A Mankodi, CR Urbinati, QP Yuan, RT Moxley, V Sansone, M Krym, ...
Human molecular genetics 10 (19), 2165-2170, 2001
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
HL Hinds, CT Ashley, JS Sutcliffe, DL Nelson, ST Warren, DE Housman, ...
Nature genetics 3 (1), 36-43, 1993
Neuropeptide expression in rat dorsal root ganglion cells and spinal cord after peripheral nerve injury with special reference to galanin
MJ Villar, R Cortes, E Theodorsson, Z Wiesenfeld-Hallin, M Schalling, ...
Neuroscience 33 (3), 587-604, 1989
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
LV Wain, GC Verwoert, PF O'Reilly, G Shi, T Johnson, AD Johnson, ...
Nature genetics, 2011
Impact of inflammation on epigenetic DNA methylation–a novel risk factor for cardiovascular disease?
P Stenvinkel, M Karimi, S Johansson, J Axelsson, M Suliman, B Lindholm, ...
Journal of internal medicine 261 (5), 488-499, 2007
Expression of the Wilms' tumor gene WT1 in the murine urogenital system.
J Pelletier, M Schalling, AJ Buckler, A Rogers, DA Haber, D Housman
Genes & development 5 (8), 1345-1356, 1991
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