Martin Schalling
Martin Schalling
professor i medicinsk genetik, Karolinska Institutet
Verified email at ki.se - Homepage
Title
Cited by
Cited by
Year
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
21172013
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103, 2011
17372011
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
16142013
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
15812013
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
P Sklar, S Ripke, LJ Scott, OA Andreassen, S Cichon, N Craddock, ...
Nature genetics 43 (10), 977, 2011
12232011
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
8971995
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
8681998
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
8441996
Neuropeptides—an overview
T Hökfelt, C Broberger, ZQD Xu, V Sergeyev, R Ubink, M Diez
Neuropharmacology 39 (8), 1337-1356, 2000
726*2000
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
591*1995
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
4752018
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
4751989
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
4311991
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
4241993
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
4232001
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
3992011
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
3952007
Low fetuin-A levels are associated with cardiovascular death: impact of variations in the gene encoding fetuin
P Stenvinkel, K Wang, AR Qureshi, J Axelsson, R Pecoits-Filho, P Gao, ...
Kidney international 67 (6), 2383-2392, 2005
3922005
The Swedish Twin Registry in the third millennium: an update
P Lichtenstein, PF Sullivan, S Cnattingius, M Gatz, S Johansson, ...
Twin research and human genetics 9 (6), 875-882, 2006
3872006
ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF
JC Engert, P Bérubé, J Mercier, C Doré, P Lepage, B Ge, JP Bouchard, ...
Nature genetics 24 (2), 120-125, 2000
3792000
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