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Results: 1 to 20 of 100

1.

Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.

Grunert M, Dorn C, Schueler M, Dunkel I, Schlesinger J, Mebus S, Alexi-Meskishvili V, Perrot A, Wassilew K, Timmermann B, Hetzer R, Berger F, Sperling SR.

Hum Mol Genet. 2014 Jun 15;23(12):3115-28. doi: 10.1093/hmg/ddu021. Epub 2014 Jan 23.

PMID:
24459294
[PubMed - in process]
2.

Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot.

Bansal V, Dorn C, Grunert M, Klaassen S, Hetzer R, Berger F, Sperling SR.

PLoS One. 2014 Jan 6;9(1):e85375. doi: 10.1371/journal.pone.0085375. eCollection 2014.

PMID:
24400131
[PubMed - in process]
Free PMC Article
3.

Application of high-throughput sequencing for studying genomic variations in congenital heart disease.

Dorn C, Grunert M, Sperling SR.

Brief Funct Genomics. 2014 Jan;13(1):51-65. doi: 10.1093/bfgp/elt040. Epub 2013 Oct 3.

PMID:
24095982
[PubMed - in process]
4.

Neuropsychiatric disease relevance of circulating anti-NMDA receptor autoantibodies depends on blood-brain barrier integrity.

Hammer C, Stepniak B, Schneider A, Papiol S, Tantra M, Begemann M, Sirén AL, Pardo LA, Sperling S, Mohd Jofrry S, Gurvich A, Jensen N, Ostmeier K, Lühder F, Probst C, Martens H, Gillis M, Saher G, Assogna F, Spalletta G, Stöcker W, Schulz TF, Nave KA, Ehrenreich H.

Mol Psychiatry. 2013 Sep 3. doi: 10.1038/mp.2013.110. [Epub ahead of print]

PMID:
23999527
[PubMed - as supplied by publisher]
5.

A pilot study of focused ultrasound thalamotomy for essential tremor.

Elias WJ, Huss D, Voss T, Loomba J, Khaled M, Zadicario E, Frysinger RC, Sperling SA, Wylie S, Monteith SJ, Druzgal J, Shah BB, Harrison M, Wintermark M.

N Engl J Med. 2013 Aug 15;369(7):640-8. doi: 10.1056/NEJMoa1300962.

PMID:
23944301
[PubMed - indexed for MEDLINE]
Free Article
6.

A single gene defect causing claustrophobia.

El-Kordi A, Kästner A, Grube S, Klugmann M, Begemann M, Sperling S, Hammerschmidt K, Hammer C, Stepniak B, Patzig J, de Monasterio-Schrader P, Strenzke N, Flügge G, Werner HB, Pawlak R, Nave KA, Ehrenreich H.

Transl Psychiatry. 2013 Apr 30;3:e254. doi: 10.1038/tp.2013.28.

PMID:
23632458
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Common variant at 16p11.2 conferring risk of psychosis.

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E; GROUP, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B; Wellcome Trust Case Control Consortium 2, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K.

Mol Psychiatry. 2014 Jan;19(1):108-14. doi: 10.1038/mp.2012.157. Epub 2012 Nov 20.

PMID:
23164818
[PubMed - in process]
Free PMC Article
8.

Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.

Meyer T, Ruppert V, Ackermann S, Richter A, Perrot A, Sperling SR, Posch MG, Maisch B, Pankuweit S; German Competence Network Heart Failure.

Eur J Hum Genet. 2013 Mar;21(3):294-300. doi: 10.1038/ejhg.2012.173. Epub 2012 Aug 15.

PMID:
22892539
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Membrane vesicle formation as a multiple-stress response mechanism enhances Pseudomonas putida DOT-T1E cell surface hydrophobicity and biofilm formation.

Baumgarten T, Sperling S, Seifert J, von Bergen M, Steiniger F, Wick LY, Heipieper HJ.

Appl Environ Microbiol. 2012 Sep;78(17):6217-24. doi: 10.1128/AEM.01525-12. Epub 2012 Jun 29.

PMID:
22752175
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Deciphering the signature of cuticular lipids with contact sex pheromone function in a parasitic wasp.

Kühbandner S, Sperling S, Mori K, Ruther J.

J Exp Biol. 2012 Jul 15;215(Pt 14):2471-8. doi: 10.1242/jeb.071217.

PMID:
22723487
[PubMed - indexed for MEDLINE]
Free Article
11.

Common variants of the genes encoding erythropoietin and its receptor modulate cognitive performance in schizophrenia.

Kästner A, Grube S, El-Kordi A, Stepniak B, Friedrichs H, Sargin D, Schwitulla J, Begemann M, Giegling I, Miskowiak KW, Sperling S, Hannke K, Ramin A, Heinrich R, Gefeller O, Nave KA, Rujescu D, Ehrenreich H.

Mol Med. 2012 Sep 7;18:1029-40. doi: 10.2119/molmed.2012.00190.

PMID:
22669473
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Erythropoietin attenuates neurological and histological consequences of toxic demyelination in mice.

Hagemeyer N, Boretius S, Ott C, Von Streitberg A, Welpinghus H, Sperling S, Frahm J, Simons M, Ghezzi P, Ehrenreich H.

Mol Med. 2012 May 9;18:628-35. doi: 10.2119/molmed.2011.00457.

PMID:
22396019
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse.

Schueler M, Zhang Q, Schlesinger J, Tönjes M, Sperling SR.

Mol Biosyst. 2012 Feb;8(2):495-503. doi: 10.1039/c1mb05363a. Epub 2011 Nov 18.

PMID:
22101280
[PubMed - indexed for MEDLINE]
14.

Circulating damage marker profiles support a neuroprotective effect of erythropoietin in ischemic stroke patients.

Ehrenreich H, Kästner A, Weissenborn K, Streeter J, Sperling S, Wang KK, Worthmann H, Hayes RL, von Ahsen N, Kastrup A, Jeromin A, Herrmann M.

Mol Med. 2011;17(11-12):1306-10. doi: 10.2119/molmed.2011.00259. Epub 2011 Sep 2.

PMID:
21912808
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Prediction of the risk of comorbid alcoholism in schizophrenia by interaction of common genetic variants in the corticotropin-releasing factor system.

Ribbe K, Ackermann V, Schwitulla J, Begemann M, Papiol S, Grube S, Sperling S, Friedrichs H, Jahn O, Sillaber I, Gefeller O, Krampe H, Ehrenreich H.

Arch Gen Psychiatry. 2011 Dec;68(12):1247-56. doi: 10.1001/archgenpsychiatry.2011.100. Epub 2011 Aug 1.

PMID:
21810631
[PubMed - indexed for MEDLINE]
16.

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

Steinberg S, de Jong S; Irish Schizophrenia Genomics Consortium, Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, Breuer R, Vassos E, Giegling I, Fraser G, Walker N, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Agartz I, Melle I, Djurovic S, Strengman E; GROUP, Jürgens G, Glenthøj B, Terenius L, Hougaard DM, Ørntoft T, Wiuf C, Didriksen M, Hollegaard MV, Nordentoft M, van Winkel R, Kenis G, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Sperling S, Rossner M, Ribolsi M, Magni V, Siracusano A, Christiansen C, Kiemeney LA, Veldink J, van den Berg L, Ingason A, Muglia P, Murray R, Nöthen MM, Sigurdsson E, Petursson H, Thorsteinsdottir U, Kong A, Rubino IA, De Hert M, Réthelyi JM, Bitter I, Jönsson EG, Golimbet V, Carracedo A, Ehrenreich H, Craddock N, Owen MJ, O'Donovan MC; Wellcome Trust Case Control Consortium 2, Ruggeri M, Tosato S, Peltonen L, Ophoff RA, Collier DA, St Clair D, Rietschel M, Cichon S, Stefansson H, Rujescu D, Stefansson K.

Hum Mol Genet. 2011 Oct 15;20(20):4076-81. doi: 10.1093/hmg/ddr325. Epub 2011 Jul 26.

PMID:
21791550
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7.

van Engelen K, Postma AV, van de Meerakker JB, Roos-Hesselink JW, Helderman-van den Enden AT, Vliegen HW, Rahman T, Baars MJ, Sels JW, Bauer U, Pickardt T, Sperling SR, Moorman AF, Keavney B, Goodship J, Klaassen S, Mulder BJ.

Neth Heart J. 2013 Mar;21(3):113-7. doi: 10.1007/s12471-011-0141-1.

PMID:
21604106
[PubMed]
Free PMC Article
18.

Systems biology approaches to heart development and congenital heart disease.

Sperling SR.

Cardiovasc Res. 2011 Jul 15;91(2):269-78. doi: 10.1093/cvr/cvr126. Epub 2011 Apr 28. Review.

PMID:
21527437
[PubMed - indexed for MEDLINE]
Free Article
19.

Expression of constitutively active erythropoietin receptor in pyramidal neurons of cortex and hippocampus boosts higher cognitive functions in mice.

Sargin D, El-Kordi A, Agarwal A, Müller M, Wojcik SM, Hassouna I, Sperling S, Nave KA, Ehrenreich H.

BMC Biol. 2011 Apr 28;9:27. doi: 10.1186/1741-7007-9-27.

PMID:
21527022
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

The cardiac transcription network modulated by Gata4, Mef2a, Nkx2.5, Srf, histone modifications, and microRNAs.

Schlesinger J, Schueler M, Grunert M, Fischer JJ, Zhang Q, Krueger T, Lange M, Tönjes M, Dunkel I, Sperling SR.

PLoS Genet. 2011 Feb;7(2):e1001313. doi: 10.1371/journal.pgen.1001313. Epub 2011 Feb 17.

PMID:
21379568
[PubMed - indexed for MEDLINE]
Free PMC Article

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