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Items: 1 to 50 of 95

1.

MEK inhibitor cobimetinib rescues a dRaf mutant lethal phenotype in Drosophila melanogaster.

Pfeifle I, Bohnekamp J, Volkhardt A, Kirsten H, Rohwedder A, Thum A, Magin TM, Kunz M.

Exp Dermatol. 2019 Jul 23. doi: 10.1111/exd.14010. [Epub ahead of print]

PMID:
31338879
2.

Food has the right of way: Evidence for prioritised processing of visual food stimuli irrespective of eating style.

Kirsten H, Seib-Pfeifer LE, Koppehele-Gossel J, Gibbons H.

Appetite. 2019 Jul 17;142:104372. doi: 10.1016/j.appet.2019.104372. [Epub ahead of print]

PMID:
31325474
3.

Refined common terminology criteria for adverse events criteria - respective systemic melanoma therapy.

Kohlmann J, Kirsten H, Simon JC, Ziemer M.

Melanoma Res. 2019 Aug;29(4):444-445. doi: 10.1097/CMR.0000000000000554. No abstract available.

PMID:
31246725
4.

Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.

Pott J, Bae YJ, Horn K, Teren A, Kühnapfel A, Kirsten H, Ceglarek U, Loeffler M, Thiery J, Kratzsch J, Scholz M.

J Clin Endocrinol Metab. 2019 Jun 6. pii: jc.2019-00757. doi: 10.1210/jc.2019-00757. [Epub ahead of print]

PMID:
31169883
5.

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, Tin A, Wang L, Chu AY, Hoppmann A, Kirsten H, Giri A, Chai JF, Sveinbjornsson G, Tayo BO, Nutile T, Fuchsberger C, Marten J, Cocca M, Ghasemi S, Xu Y, Horn K, Noce D, van der Most PJ, Sedaghat S, Yu Z, Akiyama M, Afaq S, Ahluwalia TS, Almgren P, Amin N, Ärnlöv J, Bakker SJL, Bansal N, Baptista D, Bergmann S, Biggs ML, Biino G, Boehnke M, Boerwinkle E, Boissel M, Bottinger EP, Boutin TS, Brenner H, Brumat M, Burkhardt R, Butterworth AS, Campana E, Campbell A, Campbell H, Canouil M, Carroll RJ, Catamo E, Chambers JC, Chee ML, Chee ML, Chen X, Cheng CY, Cheng Y, Christensen K, Cifkova R, Ciullo M, Concas MP, Cook JP, Coresh J, Corre T, Sala CF, Cusi D, Danesh J, Daw EW, de Borst MH, De Grandi A, de Mutsert R, de Vries APJ, Degenhardt F, Delgado G, Demirkan A, Di Angelantonio E, Dittrich K, Divers J, Dorajoo R, Eckardt KU, Ehret G, Elliott P, Endlich K, Evans MK, Felix JF, Foo VHX, Franco OH, Franke A, Freedman BI, Freitag-Wolf S, Friedlander Y, Froguel P, Gansevoort RT, Gao H, Gasparini P, Gaziano JM, Giedraitis V, Gieger C, Girotto G, Giulianini F, Gögele M, Gordon SD, Gudbjartsson DF, Gudnason V, Haller T, Hamet P, Harris TB, Hartman CA, Hayward C, Hellwege JN, Heng CK, Hicks AA, Hofer E, Huang W, Hutri-Kähönen N, Hwang SJ, Ikram MA, Indridason OS, Ingelsson E, Ising M, Jaddoe VWV, Jakobsdottir J, Jonas JB, Joshi PK, Josyula NS, Jung B, Kähönen M, Kamatani Y, Kammerer CM, Kanai M, Kastarinen M, Kerr SM, Khor CC, Kiess W, Kleber ME, Koenig W, Kooner JS, Körner A, Kovacs P, Kraja AT, Krajcoviechova A, Kramer H, Krämer BK, Kronenberg F, Kubo M, Kühnel B, Kuokkanen M, Kuusisto J, La Bianca M, Laakso M, Lange LA, Langefeld CD, Lee JJ, Lehne B, Lehtimäki T, Lieb W; Lifelines Cohort Study, Lim SC, Lind L, Lindgren CM, Liu J, Liu J, Loeffler M, Loos RJF, Lucae S, Lukas MA, Lyytikäinen LP, Mägi R, Magnusson PKE, Mahajan A, Martin NG, Martins J, März W, Mascalzoni D, Matsuda K, Meisinger C, Meitinger T, Melander O, Metspalu A, Mikaelsdottir EK, Milaneschi Y, Miliku K, Mishra PP; V. A. Million Veteran Program, Mohlke KL, Mononen N, Montgomery GW, Mook-Kanamori DO, Mychaleckyj JC, Nadkarni GN, Nalls MA, Nauck M, Nikus K, Ning B, Nolte IM, Noordam R, O'Connell J, O'Donoghue ML, Olafsson I, Oldehinkel AJ, Orho-Melander M, Ouwehand WH, Padmanabhan S, Palmer ND, Palsson R, Penninx BWJH, Perls T, Perola M, Pirastu M, Pirastu N, Pistis G, Podgornaia AI, Polasek O, Ponte B, Porteous DJ, Poulain T, Pramstaller PP, Preuss MH, Prins BP, Province MA, Rabelink TJ, Raffield LM, Raitakari OT, Reilly DF, Rettig R, Rheinberger M, Rice KM, Ridker PM, Rivadeneira F, Rizzi F, Roberts DJ, Robino A, Rossing P, Rudan I, Rueedi R, Ruggiero D, Ryan KA, Saba Y, Sabanayagam C, Salomaa V, Salvi E, Saum KU, Schmidt H, Schmidt R, Schöttker B, Schulz CA, Schupf N, Shaffer CM, Shi Y, Smith AV, Smith BH, Soranzo N, Spracklen CN, Strauch K, Stringham HM, Stumvoll M, Svensson PO, Szymczak S, Tai ES, Tajuddin SM, Tan NYQ, Taylor KD, Teren A, Tham YC, Thiery J, Thio CHL, Thomsen H, Thorleifsson G, Toniolo D, Tönjes A, Tremblay J, Tzoulaki I, Uitterlinden AG, Vaccargiu S, van Dam RM, van der Harst P, van Duijn CM, Velez Edward DR, Verweij N, Vogelezang S, Völker U, Vollenweider P, Waeber G, Waldenberger M, Wallentin L, Wang YX, Wang C, Waterworth DM, Bin Wei W, White H, Whitfield JB, Wild SH, Wilson JF, Wojczynski MK, Wong C, Wong TY, Xu L, Yang Q, Yasuda M, Yerges-Armstrong LM, Zhang W, Zonderman AB, Rotter JI, Bochud M, Psaty BM, Vitart V, Wilson JG, Dehghan A, Parsa A, Chasman DI, Ho K, Morris AP, Devuyst O, Akilesh S, Pendergrass SA, Sim X, Böger CA, Okada Y, Edwards TL, Snieder H, Stefansson K, Hung AM, Heid IM, Scholz M, Teumer A, Köttgen A, Pattaro C.

Nat Genet. 2019 Jun;51(6):957-972. doi: 10.1038/s41588-019-0407-x. Epub 2019 May 31.

6.

Necessity of transnasal gastroscopy in routine diagnostics: a patient-centred requirement analysis.

Schuldt AL, Kirsten H, Tuennemann J, Heindl M, van Bommel F, Feisthammel J, Hollenbach M, Hoffmeister A.

BMJ Open Gastroenterol. 2019 Apr 14;6(1):e000264. doi: 10.1136/bmjgast-2018-000264. eCollection 2019.

7.

[Tinea barbae profunda due to Trichophyton mentagrophytes : Case report and review].

Kirsten H, Haiduk J, Nenoff P, Uhrlaß S, Ziemer M, Simon JC.

Hautarzt. 2019 Aug;70(8):601-611. doi: 10.1007/s00105-019-4407-7. Review. German.

PMID:
31001659
8.

Association of Human FOS Promoter Variants with the Occurrence of Knee-Osteoarthritis in a Case Control Association Study.

Huber R, Kirsten H, Näkki A, Pohlers D, Thude H, Eidner T, Heinig M, Brand K, Ahnert P, Kinne RW.

Int J Mol Sci. 2019 Mar 19;20(6). pii: E1382. doi: 10.3390/ijms20061382.

9.

Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.

Timmers PR, Mounier N, Lall K, Fischer K, Ning Z, Feng X, Bretherick AD, Clark DW; eQTLGen Consortium, Agbessi M, Ahsan H, Alves I, Andiappan A, Awadalla P, Battle A, Bonder MJ, Boomsma D, Christiansen M, Claringbould A, Deelen P, van Dongen J, Esko T, Favé M, Franke L, Frayling T, Gharib SA, Gibson G, Hemani G, Jansen R, Kalnapenkis A, Kasela S, Kettunen J, Kim Y, Kirsten H, Kovacs P, Krohn K, Kronberg-Guzman J, Kukushkina V, Kutalik Z, Kähönen M, Lee B, Lehtimäki T, Loeffler M, Marigorta U, Metspalu A, van Meurs J, Milani L, Müller-Nurasyid M, Nauck M, Nivard M, Penninx B, Perola M, Pervjakova N, Pierce B, Powell J, Prokisch H, Psaty BM, Raitakari O, Ring S, Ripatti S, Rotzschke O, Ruëger S, Saha A, Scholz M, Schramm K, Seppälä I, Stumvoll M, Sullivan P, Teumer A, Thiery J, Tong L, Tönjes A, Verlouw J, Visscher PM, Võsa U, Völker U, Yaghootkar H, Yang J, Zeng B, Zhang F, Agbessi M, Ahsan H, Alves I, Andiappan A, Awadalla P, Battle A, Bonder MJ, Boomsma D, Christiansen M, Claringbould A, Deelen P, van Dongen J, Esko T, Favé M, Franke L, Frayling T, Gharib SA, Gibson G, Hemani G, Jansen R, Kalnapenkis A, Kasela S, Kettunen J, Kim Y, Kirsten H, Kovacs P, Krohn K, Kronberg-Guzman J, Kukushkina V, Kutalik Z, Kähönen M, Lee B, Lehtimäki T, Loeffler M, Marigorta U, Metspalu A, van Meurs J, Milani L, Müller-Nurasyid M, Nauck M, Nivard M, Penninx B, Perola M, Pervjakova N, Pierce B, Powell J, Prokisch H, Psaty BM, Raitakari O, Ring S, Ripatti S, Rotzschke O, Ruëger S, Saha A, Scholz M, Schramm K, Seppälä I, Stumvoll M, Sullivan P, Teumer A, Thiery J, Tong L, Tönjes A, Verlouw J, Visscher PM, Võsa U, Völker U, Yaghootkar H, Yang J, Zeng B, Zhang F, Shen X, Esko T, Kutalik Z, Wilson JF, Joshi PK.

Elife. 2019 Jan 15;8. pii: e39856. doi: 10.7554/eLife.39856.

10.

Post-mortem in situ stability of serum markers of cerebral damage and acute phase response.

Ondruschka B, Woydt L, Bernhard M, Franke H, Kirsten H, Löffler S, Pohlers D, Hammer N, Dreßler J.

Int J Legal Med. 2019 May;133(3):871-881. doi: 10.1007/s00414-018-1925-2. Epub 2018 Aug 30.

PMID:
30167776
11.

Intra-individual alterations of serum markers routinely used in forensic pathology depending on increasing post-mortem interval.

Woydt L, Bernhard M, Kirsten H, Burkhardt R, Hammer N, Gries A, Dreßler J, Ondruschka B.

Sci Rep. 2018 Aug 24;8(1):12811. doi: 10.1038/s41598-018-31252-5.

12.

34-jährige Patientin mit schwärzlichen Maculae an Handrücken und Armen.

Kirsten H, Simon JC, Kunz M.

J Dtsch Dermatol Ges. 2018 Jul;16(7):937-939. doi: 10.1111/ddg.13575_g. No abstract available.

PMID:
29989371
13.

34-year-old patient with blackish macules on the dorsa of the hands and forearms.

Kirsten H, Simon JC, Kunz M.

J Dtsch Dermatol Ges. 2018 Jul;16(7):937-938. doi: 10.1111/ddg.13575. Epub 2018 Jun 25. No abstract available.

PMID:
29938897
14.

Biomechanical properties of polymer-infiltrated ceramic crowns on one-piece zirconia implants after long-term chewing simulation.

Baumgart P, Kirsten H, Haak R, Olms C.

Int J Implant Dent. 2018 May 23;4(1):16. doi: 10.1186/s40729-018-0127-5.

15.

Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes.

Pott J, Schlegel V, Teren A, Horn K, Kirsten H, Bluecher C, Kratzsch J, Loeffler M, Thiery J, Burkhardt R, Scholz M.

Circ Genom Precis Med. 2018 May;11(5):e001992. doi: 10.1161/CIRCGEN.117.001992.

PMID:
29748315
16.

Measurement of Cerebral Biomarkers Proving Traumatic Brain Injuries in Post-Mortem Body Fluids.

Ondruschka B, Sieber M, Kirsten H, Franke H, Dreßler J.

J Neurotrauma. 2018 Sep 1;35(17):2044-2055. doi: 10.1089/neu.2017.5441. Epub 2018 Jul 6.

PMID:
29732941
17.

Human brain arousal in the resting state: a genome-wide association study.

Jawinski P, Kirsten H, Sander C, Spada J, Ulke C, Huang J, Burkhardt R, Scholz M, Hensch T, Hegerl U.

Mol Psychiatry. 2018 Apr 27. doi: 10.1038/s41380-018-0052-2. [Epub ahead of print]

PMID:
29703947
18.

Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.

Müller B, Boltze J, Czepezauer I, Hesse V; LEGASCREEN Consortium, Wilcke A, Kirsten H.

Genet Mol Biol. 2018 Jan-Mar;41(1):41-49. doi: 10.1590/1678-4685-GMB-2017-0165. Epub 2018 Feb 19.

19.

ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR.

Müller B, Schaadt G, Boltze J, Emmrich F; LEGASCREEN Consortium, Skeide MA, Neef NE, Kraft I, Brauer J, Friederici AD, Kirsten H, Wilcke A.

Brain Behav. 2017 Oct 18;7(11):e00851. doi: 10.1002/brb3.851. eCollection 2017 Nov.

20.

Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin.

Tönjes A, Scholz M, Krüger J, Krause K, Schleinitz D, Kirsten H, Gebhardt C, Marzi C, Grallert H, Ladenvall C, Heyne H, Laurila E, Kriebel J, Meisinger C, Rathmann W, Gieger C, Groop L, Prokopenko I, Isomaa B, Beutner F, Kratzsch J, Fischer-Rosinsky A, Pfeiffer A, Krohn K, Spranger J, Thiery J, Blüher M, Stumvoll M, Kovacs P.

Hum Mol Genet. 2018 Feb 1;27(3):546-558. doi: 10.1093/hmg/ddx413.

21.

Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood.

Lukowski SW, Lloyd-Jones LR, Holloway A, Kirsten H, Hemani G, Yang J, Small K, Zhao J, Metspalu A, Dermitzakis ET, Gibson G, Spector TD, Thiery J, Scholz M, Montgomery GW, Esko T, Visscher PM, Powell JE.

Nat Commun. 2017 Sep 7;8(1):483. doi: 10.1038/s41467-017-00473-z.

22.

Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis.

Rosendahl J, Kirsten H, Hegyi E, Kovacs P, Weiss FU, Laumen H, Lichtner P, Ruffert C, Chen JM, Masson E, Beer S, Zimmer C, Seltsam K, Algül H, Bühler F, Bruno MJ, Bugert P, Burkhardt R, Cavestro GM, Cichoz-Lach H, Farré A, Frank J, Gambaro G, Gimpfl S, Grallert H, Griesmann H, Grützmann R, Hellerbrand C, Hegyi P, Hollenbach M, Iordache S, Jurkowska G, Keim V, Kiefer F, Krug S, Landt O, Leo MD, Lerch MM, Lévy P, Löffler M, Löhr M, Ludwig M, Macek M, Malats N, Malecka-Panas E, Malerba G, Mann K, Mayerle J, Mohr S, Te Morsche RHM, Motyka M, Mueller S, Müller T, Nöthen MM, Pedrazzoli S, Pereira SP, Peters A, Pfützer R, Real FX, Rebours V, Ridinger M, Rietschel M, Rösmann E, Saftoiu A, Schneider A, Schulz HU, Soranzo N, Soyka M, Simon P, Skipworth J, Stickel F, Strauch K, Stumvoll M, Testoni PA, Tönjes A, Werner L, Werner J, Wodarz N, Ziegler M, Masamune A, Mössner J, Férec C, Michl P, P H Drenth J, Witt H, Scholz M, Sahin-Tóth M; all members of the PanEuropean Working group on ACP.

Gut. 2018 Oct;67(10):1855-1863. doi: 10.1136/gutjnl-2017-314454. Epub 2017 Jul 28.

23.

Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery.

Pott J, Burkhardt R, Beutner F, Horn K, Teren A, Kirsten H, Holdt LM, Schuler G, Teupser D, Loeffler M, Thiery J, Scholz M.

Atherosclerosis. 2017 Apr;259:32-40. doi: 10.1016/j.atherosclerosis.2017.02.018. Epub 2017 Feb 24.

PMID:
28282560
24.

Dyslexia risk gene relates to representation of sound in the auditory brainstem.

Neef NE, Müller B, Liebig J, Schaadt G, Grigutsch M, Gunter TC, Wilcke A, Kirsten H, Skeide MA, Kraft I, Kraus N, Emmrich F, Brauer J, Boltze J, Friederici AD.

Dev Cogn Neurosci. 2017 Apr;24:63-71. doi: 10.1016/j.dcn.2017.01.008. Epub 2017 Jan 17.

25.

Alteration of Multiple Leukocyte Gene Expression Networks is Linked with Magnetic Resonance Markers of Prognosis After Acute ST-Elevation Myocardial Infarction.

Teren A, Kirsten H, Beutner F, Scholz M, Holdt LM, Teupser D, Gutberlet M, Thiery J, Schuler G, Eitel I.

Sci Rep. 2017 Feb 3;7:41705. doi: 10.1038/srep41705.

26.

Comparing performance of modern genotype imputation methods in different ethnicities.

Roshyara NR, Horn K, Kirsten H, Ahnert P, Scholz M.

Sci Rep. 2016 Oct 4;6:34386. doi: 10.1038/srep34386.

27.

Predicting early signs of dyslexia at a preliterate age by combining behavioral assessment with structural MRI.

Kraft I, Schreiber J, Cafiero R, Metere R, Schaadt G, Brauer J, Neef NE, Müller B, Kirsten H, Wilcke A, Boltze J, Friederici AD, Skeide MA.

Neuroimage. 2016 Dec;143:378-386. doi: 10.1016/j.neuroimage.2016.09.004. Epub 2016 Sep 5.

PMID:
27608602
28.

NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school.

Skeide MA, Kraft I, Müller B, Schaadt G, Neef NE, Brauer J, Wilcke A, Kirsten H, Boltze J, Friederici AD.

Brain. 2016 Oct;139(Pt 10):2792-2803. Epub 2016 Jun 24.

PMID:
27343255
29.

Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort.

Müller B, Wilcke A, Czepezauer I, Ahnert P, Boltze J, Kirsten H; LEGASCREEN consortium.

Sci Rep. 2016 Jun 17;6:27901. doi: 10.1038/srep27901.

30.

Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.

Spada J, Scholz M, Kirsten H, Hensch T, Horn K, Jawinski P, Ulke C, Burkhardt R, Wirkner K, Loeffler M, Hegerl U, Sander C.

J Sleep Res. 2016 Dec;25(6):690-701. doi: 10.1111/jsr.12421. Epub 2016 Apr 29.

31.

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives.

Müller B, Wilcke A, Boulesteix AL, Brauer J, Passarge E, Boltze J, Kirsten H.

Hum Genet. 2016 Mar;135(3):259-72. doi: 10.1007/s00439-016-1636-z. Epub 2016 Feb 2. Review.

32.

Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood.

Burkhardt R, Kirsten H, Beutner F, Holdt LM, Gross A, Teren A, Tönjes A, Becker S, Krohn K, Kovacs P, Stumvoll M, Teupser D, Thiery J, Ceglarek U, Scholz M.

PLoS Genet. 2015 Sep 24;11(9):e1005510. doi: 10.1371/journal.pgen.1005510. eCollection 2015 Sep.

33.

Working-memory endophenotype and dyslexia-associated genetic variant predict dyslexia phenotype.

Männel C, Meyer L, Wilcke A, Boltze J, Kirsten H, Friederici AD.

Cortex. 2015 Oct;71:291-305. doi: 10.1016/j.cortex.2015.06.029. Epub 2015 Jul 22.

PMID:
26283516
34.

The role of HPV RNA transcription, immune response-related gene expression and disruptive TP53 mutations in diagnostic and prognostic profiling of head and neck cancer.

Wichmann G, Rosolowski M, Krohn K, Kreuz M, Boehm A, Reiche A, Scharrer U, Halama D, Bertolini J, Bauer U, Holzinger D, Pawlita M, Hess J, Engel C, Hasenclever D, Scholz M, Ahnert P, Kirsten H, Hemprich A, Wittekind C, Herbarth O, Horn F, Dietz A, Loeffler M; Leipzig Head and Neck Group (LHNG).

Int J Cancer. 2015 Dec 15;137(12):2846-57. doi: 10.1002/ijc.29649. Epub 2015 Jul 6.

35.

A stereotaxic, population-averaged T1w ovine brain atlas including cerebral morphology and tissue volumes.

Nitzsche B, Frey S, Collins LD, Seeger J, Lobsien D, Dreyer A, Kirsten H, Stoffel MH, Fonov VS, Boltze J.

Front Neuroanat. 2015 Jun 4;9:69. doi: 10.3389/fnana.2015.00069. eCollection 2015.

36.

Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children.

Skeide MA, Kirsten H, Kraft I, Schaadt G, Müller B, Neef N, Brauer J, Wilcke A, Emmrich F, Boltze J, Friederici AD.

Neuroimage. 2015 Sep;118:414-21. doi: 10.1016/j.neuroimage.2015.06.024. Epub 2015 Jun 12.

PMID:
26080313
37.

High acceptance of an early dyslexia screening test involving genetic analyses in Germany.

Wilcke A, Müller B, Schaadt G, Kirsten H, Boltze J; MEMBERS OF THE LEGASCREEN CONSORTIUM.

Eur J Hum Genet. 2016 Feb;24(2):178-82. doi: 10.1038/ejhg.2015.103. Epub 2015 Jun 3.

38.

Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

Kirsten H, Al-Hasani H, Holdt L, Gross A, Beutner F, Krohn K, Horn K, Ahnert P, Burkhardt R, Reiche K, Hackermüller J, Löffler M, Teupser D, Thiery J, Scholz M.

Hum Mol Genet. 2015 Aug 15;24(16):4746-63. doi: 10.1093/hmg/ddv194. Epub 2015 May 27.

39.

Genetic variants of lipase activity in chronic pancreatitis.

Kirsten H, Scholz M, Kovacs P, Grallert H, Peters A, Strauch K, Frank J, Rietschel M, Nöthen MM, Witt H, Rosendahl J.

Gut. 2016 Jan;65(1):184-5. doi: 10.1136/gutjnl-2015-309521. Epub 2015 Mar 26. No abstract available.

PMID:
25814649
40.

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis.

Fjeld K, Weiss FU, Lasher D, Rosendahl J, Chen JM, Johansson BB, Kirsten H, Ruffert C, Masson E, Steine SJ, Bugert P, Cnop M, Grützmann R, Mayerle J, Mössner J, Ringdal M, Schulz HU, Sendler M, Simon P, Sztromwasser P, Torsvik J, Scholz M, Tjora E, Férec C, Witt H, Lerch MM, Njølstad PR, Johansson S, Molven A.

Nat Genet. 2015 May;47(5):518-522. doi: 10.1038/ng.3249. Epub 2015 Mar 16.

41.

Cortical differences in preliterate children at familiar risk of dyslexia are similar to those observed in dyslexic readers.

Kraft I, Cafiero R, Schaadt G, Brauer J, Neef NE, Müller B, Kirsten H, Wilcke A, Boltze J, Friederici AD, Skeide MA.

Brain. 2015 Sep;138(Pt 9):e378. doi: 10.1093/brain/awv036. Epub 2015 Feb 19. No abstract available.

PMID:
25701065
42.

Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin.

Tönjes A, Scholz M, Breitfeld J, Marzi C, Grallert H, Gross A, Ladenvall C, Schleinitz D, Krause K, Kirsten H, Laurila E, Kriebel J, Thorand B, Rathmann W, Groop L, Prokopenko I, Isomaa B, Beutner F, Kratzsch J, Thiery J, Fasshauer M, Klöting N, Gieger C, Blüher M, Stumvoll M, Kovacs P.

PLoS Genet. 2014 Dec 18;10(12):e1004854. doi: 10.1371/journal.pgen.1004854. eCollection 2014 Dec.

43.

Three gangliogliomas: results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature.

Xu LX, Holland H, Kirsten H, Ahnert P, Krupp W, Bauer M, Schober R, Mueller W, Fritzsch D, Meixensberger J, Koschny R.

Neuropathology. 2015 Apr;35(2):148-57. doi: 10.1111/neup.12176. Epub 2014 Nov 6. Review.

PMID:
25376146
44.

Complexin2 modulates working memory-related neural activity in patients with schizophrenia.

Hass J, Walton E, Kirsten H, Turner J, Wolthusen R, Roessner V, Sponheim SR, Holt D, Gollub R, Calhoun VD, Ehrlich S.

Eur Arch Psychiatry Clin Neurosci. 2015 Mar;265(2):137-45. doi: 10.1007/s00406-014-0550-4. Epub 2014 Oct 9.

45.

Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression.

Burkhardt J, Blume M, Petit-Teixeira E, Hugo Teixeira V, Steiner A, Quente E, Wolfram G, Scholz M, Pierlot C, Migliorini P, Bombardieri S, Balsa A, Westhovens R, Barrera P, Radstake TR, Alves H, Bardin T, Prum B, Emmrich F, Cornelis F, Ahnert P, Kirsten H.

PLoS One. 2014 Aug 22;9(8):e103872. doi: 10.1371/journal.pone.0103872. eCollection 2014.

46.

Impact of pre-imputation SNP-filtering on genotype imputation results.

Roshyara NR, Kirsten H, Horn K, Ahnert P, Scholz M.

BMC Genet. 2014 Aug 12;15:88. doi: 10.1186/s12863-014-0088-5.

47.

Genetic risk variants for dyslexia on chromosome 18 in a German cohort.

Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H.

Genes Brain Behav. 2014 Mar;13(3):350-6. doi: 10.1111/gbb.12118. Epub 2014 Feb 3.

48.

Comprehensive high-resolution genomic profiling and cytogenetics of two pediatric and one adult medulloblastoma.

Holland H, Xu LX, Ahnert P, Kirsten H, Koschny R, Bauer M, Schober R, Meixensberger J, Krupp W.

Pathol Res Pract. 2013 Sep;209(9):541-7. doi: 10.1016/j.prp.2013.06.001. Epub 2013 Jul 4.

PMID:
23896263
49.

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype.

Hass J, Walton E, Kirsten H, Liu J, Priebe L, Wolf C, Karbalai N, Gollub R, White T, Roessner V, Müller KU, Paus T, Smolka MN, Schumann G; IMAGEN Consortium, Scholz M, Cichon S, Calhoun V, Ehrlich S.

PLoS One. 2013 Jun 21;8(6):e64872. doi: 10.1371/journal.pone.0064872. Print 2013.

50.

Differential allelic expression of IL13 and CSF2 genes associated with asthma.

Burkhardt J, Kirsten H, Wolfram G, Quente E, Ahnert P.

Genet Mol Biol. 2012 Jul;35(3):567-74. doi: 10.1590/S1415-47572012005000055. Epub 2012 Aug 2.

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