Martin Schalling

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Tomas HökfeltSenior professor, Karolinska InstitutetVerifierad e-postadress på ki.se
Catharina LavebrattDocent i medicinsk genetik, Karolinska InstitutetVerifierad e-postadress på ki.se
Louise NordforsDoktor i medicinsk genetik, Karolinska InstitutetVerifierad e-postadress på ki.se
Peter StenvinkelProfessor i NjurmedicinVerifierad e-postadress på ki.se
Bengt LindholmAssociate Professor, Renal Medicine and Novum, Clintec, Karolinska InstitutetVerifierad e-postadress på ki.se
Peter BaranyKarolinska Institutet, CLINTECVerifierad e-postadress på ki.se
Jeanette E JohansenKarolinska InstitutetVerifierad e-postadress på ki.se
Tina B. LonsdorfInstitute for Psychology, Biological Psychology and Cogntive Neuroscience, University of BielefeldVerifierad e-postadress på uni-bielefeld.de
Fredrik LonnqvistAssociate Professor Karolinska Institutet, CMO at QuicktestVerifierad e-postadress på quicktest.se
John R KelsoeUniversity of California San DiegoVerifierad e-postadress på ucsd.edu
Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetVerifierad e-postadress på med.unc.edu
Urban ÖsbyMD, Karolinska InstitutetVerifierad e-postadress på ki.se
Ohman ArneSenior Professor of psychology, Karolinska institutet Verifierad e-postadress på ki.se
Martin IngvarKarolinska InstitutetVerifierad e-postadress på ki.se
Kosek EProfessor Karolinska InstitutetVerifierad e-postadress på ki.se
Mikael LandénGothenburg university, Karolinska InstitutetVerifierad e-postadress på neuro.gu.se
Roberto Pecoits-FilhoProfessor of Medicine, Pontifícia Universidade Católica do ParanáVerifierad e-postadress på pucpr.br
Tomas J EkströmProfessor em. Molecular Cellbiology, Karolinska InstitutetVerifierad e-postadress på ki.se
Ole A. AndreassenProfessor of Medicine, University of Oslo, Oslo University Hospital, Oslo, NorwayVerifierad e-postadress på medisin.uio.no
Christian RückKarolinska InstitutetVerifierad e-postadress på ki.se

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Martin Schalling

professor i medicinsk genetik, Karolinska Institutet

Verifierad e-postadress på ki.se - Startsida

medicin psykiatri neurobiologi genetik histologi


Titel Sortera efter citat Sortera efter år Sortera efter titel	Citeras av Citeras av	År
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	3059	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	2429	2013
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	2387	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	2327	2011
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature genetics 43 (10), 977-983, 2011	1515	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	1462	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	1425	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	1128	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	1043	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	1024	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	1019	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	939	2021
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	716*	1995
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	529	2001
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	526	2015
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	515	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	508	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	507	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	498	2007
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	486	2000

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