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Items: 1 to 50 of 156

1.

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. 2018 Sep 14. doi: 10.1038/s41431-018-0269-1. [Epub ahead of print]

PMID:
30218098
2.

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 Aug 11. doi: 10.1002/mgg3.426. [Epub ahead of print]

3.

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. 2018 Aug 7. pii: S0920-9964(18)30479-1. doi: 10.1016/j.schres.2018.07.034. [Epub ahead of print]

PMID:
30097278
4.

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.

5.

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
6.

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. Review.

PMID:
29890179
7.

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
8.

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
9.

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
10.

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 Apr 2. doi: 10.1038/s41375-018-0125-x. [Epub ahead of print]

PMID:
29749397
11.

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.

12.

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
13.

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.

14.

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.

PMID:
29304331
15.

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.

16.

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.

17.

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.

18.

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
19.

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.

20.

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.

21.

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
22.

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.

23.

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.

24.

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
25.

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
26.

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
27.

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.

28.

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.

29.

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.

30.

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
31.

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
32.

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
33.

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.

34.

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.

35.

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes.

Sachwitz J, Strobl-Wildemann G, Fekete G, Ambrozaitytė L, Kučinskas V, Soellner L, Begemann M, Eggermann T.

BMC Med Genet. 2016 Mar 11;17:20. doi: 10.1186/s12881-016-0280-8.

36.

Letter to the Editor: Childhood trauma as a risk factor for psychosis: the confounding role of cognitive functioning.

Begemann MJ, Daalman K, Heringa SM, Schutte MJ, Sommer IE.

Psychol Med. 2016 Apr;46(5):1115-8. doi: 10.1017/S003329171500255X. Epub 2015 Dec 22. No abstract available.

PMID:
26694255
37.

First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation.

Riess A, Binder G, Ziegler J, Begemann M, Soellner L, Eggermann T.

Eur J Med Genet. 2016 Jan;59(1):1-4. doi: 10.1016/j.ejmg.2015.12.003. Epub 2015 Dec 10.

PMID:
26691664
38.

Simvastatin augmentation for recent-onset psychotic disorder: A study protocol.

Begemann MJ, Schutte MJ, Slot MI, Doorduin J, Bakker PR, van Haren NE, Sommer IE.

BBA Clin. 2015 Jul 3;4:52-58. eCollection 2015 Dec.

39.

Microdeletions of the 7q32.2 imprinted region are associated with Silver-Russell syndrome features.

Carrera IA, de Zaldívar MS, Martín R, Begemann M, Soellner L, Eggermann T.

Am J Med Genet A. 2016 Mar;170(3):743-9. doi: 10.1002/ajmg.a.37492. Epub 2015 Dec 10.

PMID:
26663145
40.

Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.

Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, Fischer U, Dityatev A, Grabe HJ, Rujescu D, Fischer A, Ehrenreich H.

EMBO Mol Med. 2015 Dec;7(12):1565-79. doi: 10.15252/emmm.201505696.

41.

Exercise Improves Clinical Symptoms, Quality of Life, Global Functioning, and Depression in Schizophrenia: A Systematic Review and Meta-analysis.

Dauwan M, Begemann MJ, Heringa SM, Sommer IE.

Schizophr Bull. 2016 May;42(3):588-99. doi: 10.1093/schbul/sbv164. Epub 2015 Nov 7. Review.

42.

Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling.

Eggermann T, Brioude F, Russo S, Lombardi MP, Bliek J, Maher ER, Larizza L, Prawitt D, Netchine I, Gonzales M, Grønskov K, Tümer Z, Monk D, Mannens M, Chrzanowska K, Walasek MK, Begemann M, Soellner L, Eggermann K, Tenorio J, Nevado J, Moore GE, Mackay DJ, Temple K, Gillessen-Kaesbach G, Ogata T, Weksberg R, Algar E, Lapunzina P.

Eur J Hum Genet. 2016 Jun;24(6):784-93. doi: 10.1038/ejhg.2015.224. Epub 2015 Oct 28. Review.

43.

Amino Acid Variation in HLA Class II Proteins Is a Major Determinant of Humoral Response to Common Viruses.

Hammer C, Begemann M, McLaren PJ, Bartha I, Michel A, Klose B, Schmitt C, Waterboer T, Pawlita M, Schulz TF, Ehrenreich H, Fellay J.

Am J Hum Genet. 2015 Nov 5;97(5):738-43. doi: 10.1016/j.ajhg.2015.09.008. Epub 2015 Oct 8.

44.

No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.

Müller A, Soellner L, Binder G, Begemann M, Eggermann T.

Am J Med Genet A. 2016 Jan;170A(1):283-4. doi: 10.1002/ajmg.a.37416. Epub 2015 Oct 8. No abstract available.

PMID:
26447000
45.

Accumulated environmental risk determining age at schizophrenia onset: a deep phenotyping-based study.

Stepniak B, Papiol S, Hammer C, Ramin A, Everts S, Hennig L, Begemann M, Ehrenreich H.

Lancet Psychiatry. 2014 Nov;1(6):444-53. doi: 10.1016/S2215-0366(14)70379-7. Epub 2014 Nov 5.

PMID:
26361199
46.

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.

Docherty LE, Rezwan FI, Poole RL, Turner CL, Kivuva E, Maher ER, Smithson SF, Hamilton-Shield JP, Patalan M, Gizewska M, Peregud-Pogorzelski J, Beygo J, Buiting K, Horsthemke B, Soellner L, Begemann M, Eggermann T, Baple E, Mansour S, Temple IK, Mackay DJ.

Nat Commun. 2015 Sep 1;6:8086. doi: 10.1038/ncomms9086.

47.

Construction of new synthetic biology tools for the control of gene expression in the cyanobacterium Synechococcus sp. strain PCC 7002.

Zess EK, Begemann MB, Pfleger BF.

Biotechnol Bioeng. 2016 Feb;113(2):424-32. doi: 10.1002/bit.25713. Epub 2015 Sep 3.

PMID:
26192329
48.

Paternally Inherited IGF2 Mutation and Growth Restriction.

Begemann M, Zirn B, Santen G, Wirthgen E, Soellner L, Büttel HM, Schweizer R, van Workum W, Binder G, Eggermann T.

N Engl J Med. 2015 Jul 23;373(4):349-56. doi: 10.1056/NEJMoa1415227. Epub 2015 Jul 8.

49.

Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management.

Soellner L, Monk D, Rezwan FI, Begemann M, Mackay D, Eggermann T.

Mol Cell Probes. 2015 Oct;29(5):282-90. doi: 10.1016/j.mcp.2015.05.003. Epub 2015 Jun 10. Review.

PMID:
26070988
50.

Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing.

Knopp C, Rudnik-Schöneborn S, Eggermann T, Bergmann C, Begemann M, Schoner K, Zerres K, Ortiz Brüchle N.

Mol Cell Probes. 2015 Oct;29(5):299-307. doi: 10.1016/j.mcp.2015.05.008. Epub 2015 May 21.

PMID:
26003401

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