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Items: 1 to 50 of 172

1.

Physical exercise improves quality of life, depressive symptoms, and cognition across chronic brain disorders: a transdiagnostic systematic review and meta-analysis of randomized controlled trials.

Dauwan M, Begemann MJH, Slot MIE, Lee EHM, Scheltens P, Sommer IEC.

J Neurol. 2019 Aug 14. doi: 10.1007/s00415-019-09493-9. [Epub ahead of print] Review.

PMID:
31414194
2.

Male infant with paternal uniparental diploidy mosaicism and a 46,XX/46,XY karyotype.

Spier I, Engels H, Stutte S, Reutter H, Bartels E, Matos Meder S, Begemann M, Mangold E, Eggermann T.

Am J Med Genet A. 2019 Aug 1. doi: 10.1002/ajmg.a.61314. [Epub ahead of print]

PMID:
31373173
3.

Atopy Increases Risk of Psychotic Experiences: A Large Population-Based Study.

Begemann MJH, Linszen MMJ, de Boer JN, Hovenga WD, Gangadin SS, Schutte MJL, Sommer IEC.

Front Psychiatry. 2019 Jul 9;10:453. doi: 10.3389/fpsyt.2019.00453. eCollection 2019.

4.

Biallelic CSGALNACT1-mutations cause a mild skeletal dysplasia.

Meyer R, Schacht S, Buschmann L, Begemann M, Kraft F, Haag N, Kochs A, Schulze A, Kurth I, Elbracht M.

Bone. 2019 Jul 17;127:446-451. doi: 10.1016/j.bone.2019.07.016. [Epub ahead of print]

PMID:
31325655
5.

Polycythemia in Patients With Hereditary Hemochromatosis: Real or Myth?

Asif S, Begemann M, Raza S.

J Clin Med Res. 2019 Jun;11(6):422-427. doi: 10.14740/jocmr3816. Epub 2019 May 10.

6.

Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations.

Eggermann T, Begemann M, Kurth I, Elbracht M.

Eur J Med Genet. 2019 Jul;62(7):103671. doi: 10.1016/j.ejmg.2019.103671. Epub 2019 May 14.

PMID:
31100449
7.

Genetically induced brain inflammation by Cnp deletion transiently benefits from microglia depletion.

Garcia-Agudo LF, Janova H, Sendler LE, Arinrad S, Steixner AA, Hassouna I, Balmuth E, Ronnenberg A, Schopf N, van der Flier FJ, Begemann M, Martens H, Weber MS, Boretius S, Nave KA, Ehrenreich H.

FASEB J. 2019 Jul;33(7):8634-8647. doi: 10.1096/fj.201900337R. Epub 2019 May 15.

PMID:
31090455
8.

Pembrolizumab in newly diagnosed EBV-negative extranodal natural killer/T-cell lymphoma: A case report.

Asif S, Begemann M, Bennett J, Fatima R, Masood A, Raza S.

Mol Clin Oncol. 2019 Mar;10(3):397-400. doi: 10.3892/mco.2019.1805. Epub 2019 Jan 23.

9.

Identification of transcription factor binding sites using ATAC-seq.

Li Z, Schulz MH, Look T, Begemann M, Zenke M, Costa IG.

Genome Biol. 2019 Feb 26;20(1):45. doi: 10.1186/s13059-019-1642-2.

10.

PDE10A mutation in two sisters with a hyperkinetic movement disorder - Response to levodopa.

Knopp C, Häusler M, Müller B, Damen R, Stoppe A, Mull M, Elbracht M, Kurth I, Begemann M.

Parkinsonism Relat Disord. 2019 Jun;63:240-242. doi: 10.1016/j.parkreldis.2019.02.007. Epub 2019 Feb 10. No abstract available.

PMID:
30777652
11.

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation.

Kraft F, Wesseler K, Begemann M, Kurth I, Elbracht M, Eggermann T.

Clin Epigenetics. 2019 Feb 15;11(1):30. doi: 10.1186/s13148-019-0629-x.

12.

DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans.

Karsai G, Kraft F, Haag N, Korenke GC, Hänisch B, Othman A, Suriyanarayanan S, Steiner R, Knopp C, Mull M, Bergmann M, Schröder JM, Weis J, Elbracht M, Begemann M, Hornemann T, Kurth I.

J Clin Invest. 2019 Mar 1;129(3):1229-1239. doi: 10.1172/JCI124159. Epub 2019 Feb 11.

13.

Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndrome.

Neuheuser L, Meyer R, Begemann M, Elbracht M, Eggermann T.

Mol Cell Probes. 2019 Apr;44:1-7. doi: 10.1016/j.mcp.2018.12.007. Epub 2019 Jan 2.

PMID:
30610903
14.

Auditory hallucinations, top-down processing and language perception: a general population study.

de Boer JN, Linszen MMJ, de Vries J, Schutte MJL, Begemann MJH, Heringa SM, Bohlken MM, Hugdahl K, Aleman A, Wijnen FNK, Sommer IEC.

Psychol Med. 2019 Jan 4:1-9. doi: 10.1017/S003329171800380X. [Epub ahead of print]

PMID:
30606279
15.

Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contractures.

Elbracht M, Kraft F, Begemann M, Holschbach P, Mull M, Kabat IM, Müller B, Häusler M, Kurth I, Hehr U.

Mol Genet Genomic Med. 2018 Nov;6(6):1255-1260. doi: 10.1002/mgg3.490. Epub 2018 Nov 4.

16.

Efficacy of different types of cognitive enhancers for patients with schizophrenia: a meta-analysis.

Sinkeviciute I, Begemann M, Prikken M, Oranje B, Johnsen E, Lei WU, Hugdahl K, Kroken RA, Rau C, Jacobs JD, Mattaroccia S, Sommer IE.

NPJ Schizophr. 2018 Oct 25;4(1):22. doi: 10.1038/s41537-018-0064-6.

17.

Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers.

Soellner L, Kraft F, Sauer S, Begemann M, Kurth I, Elbracht M, Eggermann T.

Eur J Hum Genet. 2019 Jan;27(1):42-48. doi: 10.1038/s41431-018-0269-1. Epub 2018 Sep 14.

PMID:
30218098
18.

Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients.

Eggermann T, Ledig S, Begemann M, Elbracht M, Kurth I, Wieacker P.

Mol Genet Genomic Med. 2018 Nov;6(6):1225-1228. doi: 10.1002/mgg3.426. Epub 2018 Aug 11.

19.

The efficacy of computerized cognitive drill and practice training for patients with a schizophrenia-spectrum disorder: A meta-analysis.

Prikken M, Konings MJ, Lei WU, Begemann MJH, Sommer IEC.

Schizophr Res. 2019 Feb;204:368-374. doi: 10.1016/j.schres.2018.07.034. Epub 2018 Aug 7.

PMID:
30097278
20.

Genome-wide association study results for educational attainment aid in identifying genetic heterogeneity of schizophrenia.

Bansal V, Mitjans M, Burik CAP, Linnér RK, Okbay A, Rietveld CA, Begemann M, Bonn S, Ripke S, de Vlaming R, Nivard MG, Ehrenreich H, Koellinger PD.

Nat Commun. 2018 Aug 6;9(1):3078. doi: 10.1038/s41467-018-05510-z.

21.

Immediate and long-term effects of bilateral electroconvulsive therapy on cognitive functioning in patients with a depressive disorder.

Nuninga JO, Claessens TFI, Somers M, Mandl R, Nieuwdorp W, Boks MP, Bakker S, Begemann MJH, Heringa S, Sommer IEC.

J Affect Disord. 2018 Oct 1;238:659-665. doi: 10.1016/j.jad.2018.06.040. Epub 2018 Jun 20.

PMID:
29966930
22.

Clinical use of semantic space models in psychiatry and neurology: A systematic review and meta-analysis.

de Boer JN, Voppel AE, Begemann MJH, Schnack HG, Wijnen F, Sommer IEC.

Neurosci Biobehav Rev. 2018 Oct;93:85-92. doi: 10.1016/j.neubiorev.2018.06.008. Epub 2018 Jun 8.

PMID:
29890179
23.

Childhood abuse and white matter integrity in bipolar disorder patients and healthy controls.

Stevelink R, Abramovic L, Verkooijen S, Begemann MJH, Sommer IEC, Boks MP, Mandl RCW, van Haren NEM, Vinkers CH.

Eur Neuropsychopharmacol. 2018 Jul;28(7):807-817. doi: 10.1016/j.euroneuro.2018.05.003. Epub 2018 Jun 2.

PMID:
29866576
24.

Convergence of placenta biology and genetic risk for schizophrenia.

Ursini G, Punzi G, Chen Q, Marenco S, Robinson JF, Porcelli A, Hamilton EG, Mitjans M, Maddalena G, Begemann M, Seidel J, Yanamori H, Jaffe AE, Berman KF, Egan MF, Straub RE, Colantuoni C, Blasi G, Hashimoto R, Rujescu D, Ehrenreich H, Bertolino A, Weinberger DR.

Nat Med. 2018 Jun;24(6):792-801. doi: 10.1038/s41591-018-0021-y. Epub 2018 May 28.

PMID:
29808008
25.

Violent aggression predicted by multiple pre-adult environmental hits.

Mitjans M, Seidel J, Begemann M, Bockhop F, Moya-Higueras J, Bansal V, Wesolowski J, Seelbach A, Ibáñez MI, Kovacevic F, Duvar O, Fañanás L, Wolf HU, Ortet G, Zwanzger P, Klein V, Lange I, Tänzer A, Dudeck M, Penke L, van Elst LT, Bittner RA, Schmidmeier R, Freese R, Müller-Isberner R, Wiltfang J, Bliesener T, Bonn S, Poustka L, Müller JL, Arias B, Ehrenreich H.

Mol Psychiatry. 2018 May 24. doi: 10.1038/s41380-018-0043-3. [Epub ahead of print]

PMID:
29795411
26.

Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.

Kirschner M, Maurer A, Wlodarski MW, Ventura Ferreira MS, Bouillon AS, Halfmeyer I, Blau W, Kreuter M, Rosewich M, Corbacioglu S, Beck J, Schwarz M, Bittenbring J, Radsak MP, Wilk CM, Koschmieder S, Begemann M, Kurth I, Schemionek M, Brümmendorf TH, Beier F.

Leukemia. 2018 Aug;32(8):1762-1767. doi: 10.1038/s41375-018-0125-x. Epub 2018 Apr 2.

PMID:
29749397
27.

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring.

Begemann M, Rezwan FI, Beygo J, Docherty LE, Kolarova J, Schroeder C, Buiting K, Chokkalingam K, Degenhardt F, Wakeling EL, Kleinle S, González Fassrainer D, Oehl-Jaschkowitz B, Turner CLS, Patalan M, Gizewska M, Binder G, Bich Ngoc CT, Chi Dung V, Mehta SG, Baynam G, Hamilton-Shield JP, Aljareh S, Lokulo-Sodipe O, Horton R, Siebert R, Elbracht M, Temple IK, Eggermann T, Mackay DJG.

J Med Genet. 2018 Jul;55(7):497-504. doi: 10.1136/jmedgenet-2017-105190. Epub 2018 Mar 24.

28.

Uncoupling the widespread occurrence of anti-NMDAR1 autoantibodies from neuropsychiatric disease in a novel autoimmune model.

Pan H, Oliveira B, Saher G, Dere E, Tapken D, Mitjans M, Seidel J, Wesolowski J, Wakhloo D, Klein-Schmidt C, Ronnenberg A, Schwabe K, Trippe R, Mätz-Rensing K, Berghoff S, Al-Krinawe Y, Martens H, Begemann M, Stöcker W, Kaup FJ, Mischke R, Boretius S, Nave KA, Krauss JK, Hollmann M, Lühder F, Ehrenreich H.

Mol Psychiatry. 2018 Feb 9. doi: 10.1038/s41380-017-0011-3. [Epub ahead of print]

PMID:
29426955
29.

The effect of raloxifene augmentation in men and women with a schizophrenia spectrum disorder: a systematic review and meta-analysis.

de Boer J, Prikken M, Lei WU, Begemann M, Sommer I.

NPJ Schizophr. 2018 Jan 10;4(1):1. doi: 10.1038/s41537-017-0043-3. Review.

30.

Rapid and Scalable Characterization of CRISPR Technologies Using an E. coli Cell-Free Transcription-Translation System.

Marshall R, Maxwell CS, Collins SP, Jacobsen T, Luo ML, Begemann MB, Gray BN, January E, Singer A, He Y, Beisel CL, Noireaux V.

Mol Cell. 2018 Jan 4;69(1):146-157.e3. doi: 10.1016/j.molcel.2017.12.007.

31.

Microglia ablation alleviates myelin-associated catatonic signs in mice.

Janova H, Arinrad S, Balmuth E, Mitjans M, Hertel J, Habes M, Bittner RA, Pan H, Goebbels S, Begemann M, Gerwig UC, Langner S, Werner HB, Kittel-Schneider S, Homuth G, Davatzikos C, Völzke H, West BL, Reif A, Grabe HJ, Boretius S, Ehrenreich H, Nave KA.

J Clin Invest. 2018 Feb 1;128(2):734-745. doi: 10.1172/JCI97032. Epub 2017 Dec 18.

32.

The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?

Eggermann T, Oehl-Jaschkowitz B, Dicks S, Thomas W, Kanber D, Albrecht B, Begemann M, Kurth I, Beygo J, Buiting K.

Mol Genet Genomic Med. 2017 Nov;5(6):668-677. doi: 10.1002/mgg3.324. Epub 2017 Sep 22.

33.

Sexual dimorphism of AMBRA1-related autistic features in human and mouse.

Mitjans M, Begemann M, Ju A, Dere E, Wüstefeld L, Hofer S, Hassouna I, Balkenhol J, Oliveira B, van der Auwera S, Tammer R, Hammerschmidt K, Völzke H, Homuth G, Cecconi F, Chowdhury K, Grabe H, Frahm J, Boretius S, Dandekar T, Ehrenreich H.

Transl Psychiatry. 2017 Oct 10;7(10):e1247. doi: 10.1038/tp.2017.213.

34.

Auditory hallucinations across the lifespan: a systematic review and meta-analysis.

Maijer K, Begemann MJH, Palmen SJMC, Leucht S, Sommer IEC.

Psychol Med. 2018 Apr;48(6):879-888. doi: 10.1017/S0033291717002367. Epub 2017 Sep 28.

PMID:
28956518
35.

Precise insertion and guided editing of higher plant genomes using Cpf1 CRISPR nucleases.

Begemann MB, Gray BN, January E, Gordon GC, He Y, Liu H, Wu X, Brutnell TP, Mockler TC, Oufattole M.

Sci Rep. 2017 Sep 14;7(1):11606. doi: 10.1038/s41598-017-11760-6.

36.

Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction.

Chantot-Bastaraud S, Stratmann S, Brioude F, Begemann M, Elbracht M, Graul-Neumann L, Harbison M, Netchine I, Eggermann T.

Mol Cytogenet. 2017 Jul 25;10:28. doi: 10.1186/s13039-017-0329-1. eCollection 2017.

37.

NLRP genes and their role in preeclampsia and multi-locus imprinting disorders.

Soellner L, Kopp KM, Mütze S, Meyer R, Begemann M, Rudnik S, Rath W, Eggermann T, Zerres K.

J Perinat Med. 2018 Feb 23;46(2):169-173. doi: 10.1515/jpm-2016-0405.

PMID:
28753543
38.

A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms.

Lepeta K, Purzycka KJ, Pachulska-Wieczorek K, Mitjans M, Begemann M, Vafadari B, Bijata K, Adamiak RW, Ehrenreich H, Dziembowska M, Kaczmarek L.

EMBO Mol Med. 2017 Aug;9(8):1100-1116. doi: 10.15252/emmm.201707723.

39.

Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring.

Soellner L, Begemann M, Degenhardt F, Geipel A, Eggermann T, Mangold E.

Eur J Hum Genet. 2017 Aug;25(8):924-929. doi: 10.1038/ejhg.2017.94. Epub 2017 May 31.

40.

Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management.

Meyer R, Soellner L, Begemann M, Dicks S, Fekete G, Rahner N, Zerres K, Elbracht M, Eggermann T.

J Pediatr. 2017 Aug;187:206-212.e1. doi: 10.1016/j.jpeds.2017.04.018. Epub 2017 May 19.

PMID:
28529015
41.

Letter to the Editor: Beyond childhood trauma - stressful events early and later in life in relation to psychotic experiences.

Begemann MJH, Stotijn E, Schutte MJL, Heringa SM, Sommer IEC.

Psychol Med. 2017 Nov;47(15):2731-2736. doi: 10.1017/S0033291717000538. Epub 2017 Apr 17. No abstract available.

PMID:
28414010
42.

Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself.

Scheuvens R, Begemann M, Soellner L, Meschede D, Raabe-Meyer G, Elbracht M, Schubert R, Eggermann T.

Clin Genet. 2017 Jul;92(1):45-51. doi: 10.1111/cge.12958. Epub 2017 Mar 8.

PMID:
28032339
43.

OTTO: a new strategy to extract mental disease-relevant combinations of GWAS hits from individuals.

Ehrenreich H, Mitjans M, Van der Auwera S, Centeno TP, Begemann M, Grabe HJ, Bonn S, Nave KA.

Mol Psychiatry. 2018 Feb;23(2):476-486. doi: 10.1038/mp.2016.208. Epub 2016 Dec 6.

44.

CRISPR interference as a titratable, trans-acting regulatory tool for metabolic engineering in the cyanobacterium Synechococcus sp. strain PCC 7002.

Gordon GC, Korosh TC, Cameron JC, Markley AL, Begemann MB, Pfleger BF.

Metab Eng. 2016 Nov;38:170-179. doi: 10.1016/j.ymben.2016.07.007. Epub 2016 Jul 29.

45.

Relationship between neuroticism, childhood trauma and cognitive-affective responses to auditory verbal hallucinations.

So SH, Begemann MJ, Gong X, Sommer IE.

Sci Rep. 2016 Oct 4;6:34401. doi: 10.1038/srep34401.

46.

Recent Advances in Imprinting Disorders.

Soellner L, Begemann M, Mackay DJ, Grønskov K, Tümer Z, Maher ER, Temple IK, Monk D, Riccio A, Linglart A, Netchine I, Eggermann T.

Clin Genet. 2017 Jan;91(1):3-13. doi: 10.1111/cge.12827. Epub 2016 Aug 4. Review.

PMID:
27363536
47.

Childhood Trauma as a Neglected Factor in Psychotic Experiences and Cognitive Functioning.

Begemann MJ, Heringa SM, Sommer IE.

JAMA Psychiatry. 2016 Aug 1;73(8):875-6. doi: 10.1001/jamapsychiatry.2016.0924. No abstract available.

PMID:
27331876
48.

Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.

Bens S, Kolarova J, Beygo J, Buiting K, Caliebe A, Eggermann T, Gillessen-Kaesbach G, Prawitt D, Thiele-Schmitz S, Begemann M, Enklaar T, Gutwein J, Haake A, Paul U, Richter J, Soellner L, Vater I, Monk D, Horsthemke B, Ammerpohl O, Siebert R.

Epigenomics. 2016 Jun;8(6):801-16. doi: 10.2217/epi-2016-0007. Epub 2016 Jun 20.

PMID:
27323310
49.

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.

Eggermann K, Bliek J, Brioude F, Algar E, Buiting K, Russo S, Tümer Z, Monk D, Moore G, Antoniadi T, Macdonald F, Netchine I, Lombardi P, Soellner L, Begemann M, Prawitt D, Maher ER, Mannens M, Riccio A, Weksberg R, Lapunzina P, Grønskov K, Mackay DJ, Eggermann T.

Eur J Hum Genet. 2016 Oct;24(10):1377-87. doi: 10.1038/ejhg.2016.45. Epub 2016 May 11.

50.

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation.

Bohne F, Langer D, Martiné U, Eider CS, Cencic R, Begemann M, Elbracht M, Bülow L, Eggermann T, Zechner U, Pelletier J, Zabel BU, Enklaar T, Prawitt D.

Clin Epigenetics. 2016 May 4;8:47. doi: 10.1186/s13148-016-0215-4. eCollection 2016.

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