Kalman JL, Papiol S, Grigoroiu-Serbanescu M, Adorjan K, Anderson-Schmidt H, Brosch K, Budde M, Comes AL, Gade K, Forstner A, Grotegerd D, Hahn T, Heilbronner M, Heilbronner U, Heilmann-Heimbach S, Klöhn-Saghatolislam F, Kohshour MO, Meinert S, Meller T, Mullins N, Nenadić I, Nöthen MM, Pfarr JK, Reich-Erkelenz D, Rietschel M, Ringwald KG, Schaupp S, Schulte EC, Senner F, Stein F, Streit F, Vogl T, Falkai P, Dannlowski U, Kircher T, Schulze TG, Andlauer TFM (2021): Genetic risk for psychiatric illness is associated with the number of hospitalizations of bipolar disorder patients. Journal of Affective Disorders doi:10.1016/j.jad.2021.09.073 View article
Gergei I*, Zheng J*, Andlauer TFM* (shared first), Brandenburg V, Mirza-Schreiber N, Müller-Myhsok B, Krämer BK, Richard D, Falk L, Movérare-Skrtic S, Ohlsson C, Smith GD, März W, Voelkl J, Tobias JH (2021): GWAS meta-analysis followed by Mendelian randomisation revealed potential control mechanisms for circulating α-klotho levels. Human Molecular Genetics doi:10.1093/hmg/ddab263 View article
Bussas M, Grahl S, Pongratz V, Berthele A, Gasperi C, Andlauer TFM, Gaser C, Kirschke JS, Wiestler B, Zimmer C, Hemmer B, Mühlau M (2021): Gray matter atrophy in relapsing-remitting multiple sclerosis is associated with white matter lesions in connecting fibers. Multiple Sclerosis doi:10.1177/13524585211044957 View article
Kalman JL, Olde Loohuis LM, Vreeker A, …, …, Andlauer TFM*, Schulze TG*, Ophoff RA* (shared last) (2021): Characterisation of age and polarity at onset in bipolar disorder. The British Journal of Psychiatry doi:10.1192/bjp.2021.102 View article
Cirac A, Tsaktanis T, Beyer T, Linnerbauer M, Andlauer TFM, Grummel V, Nirschl L, Loesslein L, Quintana FJ, Hemmer B, Rothhammer V (2021): The Aryl Hydrocarbon Receptor-Dependent TGF-α/VEGF-B Ratio Correlates With Disease Subtype and Prognosis in Multiple Sclerosis. Neurology Neuroimmunology & Neuroinflammation 8(5):e1043 View article
Wendel B, Papiol S, Andlauer TFM, Zimmermann J, Wiltfang J, Spitzer C, Senner F, Schulte EC, Schmauß M, Schaupp SK, Repple J, Reininghaus E, Reimer J, Reich-Erkelenz D, Opel N, Nenadić I, Meinert S, Konrad C, Klöhn-Saghatolislam F, Kircher T, Kalman JL, Juckel G, Jansen A, Jäger M, Heilbronner M, von Hagen M, Gade K, Figge C, Fallgatter AJ, Dietrich DE, Dannlowski U, Comes AL, Budde M, Baune BT, Arolt V, Anghelescu IG, Anderson-Schmidt H, Adorjan K, Falkai P, Schulze TG, Bickeböller H, Heilbronner U (2021): A genome-wide association study of the longitudinal course of executive functions. Translational Psychiatry 11(1):386 View article
Ringwald KG, Meller T, Schmitt S, Andlauer TFM, Stein F, Brosch K, Pfarr JK, Steinsträter O, Meinert S, Lemke H, Waltemate L, Thiel K, Grotegerd D, Enneking V, Klug M, Jansen A, Forstner AJ, Streit F, Witt SH, Rietschel M, Müller-Myhsok B, Nöthen MM, Dannlowski U, Krug A, Nenadić I, Kircher T (2021): Interaction of developmental factors and ordinary stressful life events on brain structure in adults. NeuroImage: Clinical 30:102683 View article
Pelin H, Ising M, Stein F, Meinert S, Meller T, Brosch K, Winter NR, Krug A, Leenings R, Lemke H, Nenadić I, Heilmann-Heimbach S, Forstner AJ, Nöthen MM, Opel N, Repple J, Pfarr J, Ringwald K, Schmitt S, Thiel K, Waltemate L, Winter A, Streit F, Witt S, Rietschel M, Dannlowski U, Kircher T, Hahn T, Müller-Myhsok B, Andlauer TFM (2021): Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning. Neuropsychopharmacology doi: 10.1038/s41386-021-01051-0 View article
Morneau-Vaillancourt G, Andlauer TFM, Ouellet-Morin I, Paquin S, Brendgen MR, Vitaro F, Gouin JP, Séguin JR, Gagnon É, Cheesman R, Forget-Dubois N, Rouleau GA, Turecki G, Tremblay RE, Côté SM, Dionne G, Boivin M (2021): Polygenic scores differentially predict developmental trajectories of subtypes of social withdrawal in childhood. The Journal of Child Psychology and Psychiatry doi: 10.1111/jcpp.13459 View article
Zeng L, Moser S, Mirza-Schreiber N, Lamina C, Coassin S, Nelson CP, Annilo T, Franzén O, Kleber ME, Mack S, Andlauer TFM, Jiang B, Stiller B, Li L, Willenborg C, Munz M, Kessler T, Kastrati A, Laugwitz KL, Erdmann J, Moebus S, Nöthen MM, Peters A, Strauch K, Müller-Nurasyid M, Gieger C, Meitinger T, Steinhagen-Thiessen E, März W, Metspalu A, Björkegren JLM, Samani NJ, Kronenberg F, Müller-Myhsok B, Schunkert H (2021): Cis-epistasis at the LPA locus and risk of cardiovascular diseases. Cardiovascular Research doi: 10.1093/cvr/cvab136 View article
Andlauer TFM, Mühleisen TW, Hoffstaedter F, Teumer A, Wittfeld K, Teuber A, Reinbold CS, Grotegerd D, Bülow R, Caspers S, Dannlowski U, Herms S, Hoffmann P, Kircher T, Minnerup H, Moebus S, Nenadić I, Teismann H, Völker U, Etkin A, Berger K, Grabe HJ, Nöthen MM, Amunts K, Eickhoff SB, Sämann PG, Müller-Myhsok B, Cichon S (2021): Genetic factors influencing a neurobiological substrate for psychiatric disorders. Translational Psychiatry 11(1):192 View article
Vandebergh M, Andlauer TFM, Zhou Y, Mallants K, Held F, Aly L, Taylor BV, Hemmer B, Dubois B, Goris A (2021): Genetic variation in WNT9B increases relapse hazard in multiple sclerosis. Annals of Neurology doi: 10.1002/ana.26061 View article
Kendall KM, van Assche E, Andlauer TFM, Choi KW, Luykx JJ, Schulte EC, Lu Y (2021): The genetic basis of major depression. Psychological Medicine doi: 10.1017/S0033291721000441 View article
Heilbronner U, Papiol S, Budde M, Andlauer TFM, Strohmaier J, Streit F, Frank J, Degenhardt F, Heilmann-Heimbach S, Witt SH, Forstner AJ, Loerbroks A, Amelang M, Stürmer T, Müller-Myhsok B, Nöthen MM, Rietschel M, Schulze TG (2021): “The Heidelberg Five” personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Med Genet B Neuropsychiatr Genet doi: 10.1002/ajmg.b.32837 View article
Guzman-Parra J, Streit F, Forstner AJ, Strohmaier J, González MJ, Gil Flores S, Cabaleiro Fabeiro FJ, del Río Noriega F, Perez Perez F, Haro González J, Orozco Diaz G, de Diego-Otero Y, Moreno-Kuestner B, Auburger G, Degenhardt F, Heilmann-Heimbach S, Herms S, Hoffmann P, Frank J, Foo JC, Sirignano L, Witt SH, Cichon C, Rivas F, Mayoral F, Nöthen MM, Andlauer TFM*, Rietschel M* (shared last) (2021): Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families. Translational Psychiatry 11(1):31 View article
Ostkamp P, Salmen A, Pignolet B, Görlich D, Andlauer TFM, Schulte-Mecklenbeck A, Gonzalez-Escamilla G, Bucciarelli F, Gennero I, Breuer J, Antony G, Schneider-Hohendorf T, Mykicki N, Bayas A, Then Bergh F, Bittner S, Hartung HP, Friese MA, Linker RA, Luessi F, Lehmann-Horn K, Mühlau M, Paul F, Stangel M, Tackenberg B, Tumani H, Warnke C, Weber F, Wildemann B, Zettl UK, Ziemann U, Müller-Myhsok B, Kümpfel T, Klotz L, Meuth SG, Zipp F, Hemmer B, Hohlfeld R, Brassat D, Gold R, Gross CC, Lukas C, Groppa S, Loser K, Wiendl H, Schwab N; German Competence Network Multiple Sclerosis (KKNMS) and the BIONAT Network (2021): Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity. PNAS 118(1):e2018457118 View article
Three additional publications as part of the MDD Working Group of the Psychiatric Genomics Consortium:
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. JAMA Psychiatry e212099 View abstract
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts. Biological Psychiatry S0006-3223(21)01263-4 View abstract
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biological Psychiatry S0006-3223(21)01139-2 View abstract
2020
Heitmann H, Andlauer TFM, Korn T, Mühlau M, Henningsen P, Hemmer B, Ploner M. (2020): Fatigue, depression, and pain in multiple sclerosis: How neuroinflammation translates into dysfunctional reward processing and anhedonic symptoms. Multiple Sclerosis Journal doi:10.1177/1352458520972279 View article
Andlauer TFM, Link J, Martin D, Ryner M, Hermanrud C, Grummel V, Auer M, Hegen H, Aly L, Gasperi C, Knier B, Müller-Myhsok B, Jensen PEH, Sellebjerg F, Kockum I, Olsson T, Pallardy M, Spindeldreher S, Deisenhammer F, Fogdell-Hahn A, Hemmer B & on behalf of the ABIRISK consortium (2020): Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. BMC Medicine 18:298 View article
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, Demonet J, Morris AP, Hulslander J, Willcutt EJ, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Kirsten H, Müller B, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B & Schulte-Körne B (2020): Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry doi:10.1038/s41380-020-00898-x View article
Faber H, Kurtoic D, Krishnamoorthy G, Weber P, Pütz P, Müller-Myhsok B, Weber F, Andlauer TFM (2020): Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes. Frontiers in Immunology 11:2165 View article
Goltermann J, Redlich R, Grotegerd D, Dohm K, Leehr EJ, Böhnlein J, Förster K, Meinert S, Enneking V, Richter M, Repple J, DeVillers I, Kloecker M, Jansen A, Krug A, Nenadić I, Brosch K, Meller T, Stein F, Schmitt S, Rietschel M, Streit F, Witt SH, Forstner AJ, Nöthen MM, Baune BT, Andlauer TFM, Kircher T, Opel N, Dannlowski U (2020): Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition. Neuropsychopharmacology doi:10.1038/s41386-020-00794-6 View article
Andlauer TFM, Nöthen MM (2020): Polygenic scores for psychiatric disease: from research tool to clinical application. medizinische genetik 32(1) 39-45 View article
Nenadić I, Meller T, Schmitt S, Stein F, Brosch K, Mosebach J, Ettinger U, Grant P, Meinert S, Opel N, Lemke H, Fingas S, Förster K, Hahn T, Jansen A, Andlauer TFM, Forstner AJ, Heilmann-Heimbach S, Hall ASM, Awasthi S, Ripke S, Witt SH, Rietschel M, Müller-Myhsok B, Nöthen MM, Dannlowski U, Krug A, Streit F, Kircher T (2020): Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects. Psychological Medicine doi:10.1017/S0033291720002822 View abstract
Gasperi C, Andlauer TFM, Keating A, Knier B, Klein A, Pernpeintner V, Lichtner P, Gold R, Zipp F, Then Bergh F, Stangel M, Tumani H, Wildemann B, Wiendl H, Bayas A, Kümpfel T, Zettl UK, Linker RA, Ziemann U, Knop M, Warnke C, Friese MA, Paul F, Tackenberg B, Berthele A, Hemmer B (2020): Genetic determinants of the humoral immune response in MS. Neurology Neuroimmunology & Neuroinflammation 7(5):e827 View abstract
Hagenaars SP, Coleman JRI, Choi SW, Gaspar H, Adams MJ, Howard DM, Hodgson K, Traylor M, Air TM, Andlauer TFM, Arolt V, Baune BT, Binder EB, Blackwood DHR, Boomsma DI, Campbell A, Cearns M, Czamara D, Dannlowski U, Domschke K, de Geus EJC, Hamilton SP, Hayward C, Hickie IB, Hottenga JJ, Ising M, Jones I, Jones L, Kutalik Z, Lucae S, Martin NG, Milaneschi Y, Mueller-Myhsok B, Owen MJ, Padmanabhan S, Penninx BWJH, Pistis G, Porteous DJ, Preisig M, Ripke S, Shyn SI, Sullivan PF, Whitfield JB, Wray NR, McIntosh AM, Deary IJ, Breen G, Lewis CM (2020): Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics doi:10.1002/ajmg.b.32807 View abstract
Aly L, Havla J, Lepennetier G, Andlauer TFM, Sie C, Strauß EM, Hoshi MM, Kümpfel T, Hiltensperger M, Mitsdoerffer M, Mühlau M, Zimmer C, Hemmer B, Korn T, Knier B (2020): Inner retinal layer thinning in radiologically isolated syndrome predicts conversion to multiple sclerosis. European Journal of Neurology doi:10.1111/ene.14416 View abstract
Krug A, Wöhr M, Seffer D, Rippberger H, Sungur AÖ, Dietsche B, Stein F, Sivalingam S, Forstner AJ, Witt SH, Dukal H, Streit F, Maaser A, Heilmann-Heimbach S, Andlauer TFM, Herms S, Hoffmann P, Rietschel M, Nöthen MM, Lackinger M, Schratt G, Koch M, Schwarting RKW, Kircher T (2020): Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study. Molecular Autism 11(1):54 View abstract
Cai N, Revez JA, Adams MJ, Andlauer TFM, Breen G, Byrne EM, Clarke TK, Forstner AJ, Grabe HJ, Hamilton SP, Levinson DF, Lewis CM, Lewis G, Martin NG, Milaneschi Y, Mors O, Müller-Myhsok B, Penninx BWJH, Perlis RH, Pistis G, Potash JB, Preisig M, Shi J, Smoller JW, Streit F, Tiemeier H, Uher R, Van der Auwera S, Viktorin A, Weissman MM, MDD Working Group of the Psychiatric Genomics Consortium, Kendler KS, Flint J (2020): Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nature Genetics 52(4):437-447 View abstract
Dwyer DB, Kalman JL, Budde M, Kambeitz J, Ruef A, Antonucci LA, Kambeitz-Ilankovic L, Hasan A, Kondofersky I, Anderson-Schmidt H, Gade K, Reich-Erkelenz D, Adorjan K, Senner F, Schaupp S, Andlauer TFM, Comes AL, Schulte EC, Klöhn-Saghatolislam F, Gryaznova A, Hake M, Bartholdi K, Flatau-Nagel L, Reitt M, Quast S, Stegmaier S, Meyers M, Emons B, Haußleiter IS, Juckel G, Nieratschker V, Dannlowski U, Yoshida T, Schmauß M, Zimmermann J, Reimer J, Wiltfang J, Reininghaus E, Anghelescu IG, Arolt V, Baune BT, Konrad C, Thiel A, Fallgatter AJ, Figge C, von Hagen M, Koller M, Lang FU, Wigand ME, Becker T, Jäger M, Dietrich DE, Scherk H, Spitzer C, Folkerts H, Witt SH, Degenhardt F, Forstner AJ, Rietschel M, Nöthen MM, Mueller N, Papiol S, Heilbronner U, Falkai P, Schulze TG, Koutsouleris N (2020): An Investigation of Psychosis Subgroups With Prognostic Validation and Exploration of Genetic Underpinnings: The PsyCourse Study. JAMA Psychiatry 77(5):523-533 View abstract
Comes AL, Czamara D, Adorjan K, Anderson-Schmidt H, Andlauer TFM, Budde M, Gade K, Hake M, Kalman JL, Papiol S, Reich-Erkelenz D, Klöhn-Saghatolislam F, Schaupp SK, Schulte EC, Senner F, Juckel G, Schmauß M, Zimmermann J, Reimer J, Reininghaus E, Anghelescu IG, Konrad C, Thiel A, Figge C, von Hagen M, Koller M, Dietrich DE, Stierl S, Scherk H, Witt SH, Sivalingam S, Degenhardt F, Forstner AJ, Rietschel M, Nöthen MM, Wiltfang J, Falkai P, Schulze TG, Heilbronner U (2020): The Role of Environmental Stress and DNA Methylation in the Longitudinal Course of Bipolar Disorder International Journal of Bipolar Disorders 8(1):9 View abstract
Arloth J, Eraslan G, Andlauer TFM, Martins J, Iurato S, Kühnel B, Waldenberger M, Frank J, Gold R, Hemmer B, Luessi F, Nischwitz S, Paul F, Wiendl H, Gieger C, Heilmann-Heimbach S, Kacprowski T, Laudes M, Meitinger T, Peters A, Rawal S, Strauch K, Lucae S, Müller-Myhsok B, Rietschel M, Theis FJ, Binder EB, Mueller NS (2020): DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. PLOS Computational Biology, doi:10.1371/journal.pcbi.1007616 View abstract
Three additional publications as part of the MDD Working Group of the Psychiatric Genomics Consortium:
Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry doi:10.1038/s41380-020-0689-5 View abstract
Genome-wide Gene-Environment Analyses of Major Depressive Disorder and Reported Lifetime Traumatic Experiences in UK Biobank. Molecular Psychiatry 25(7):1430-1446 View abstract
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank. Nature Communications 11(1):2301 View abstract
2019
Cross-Disorder Group of the Psychiatric Genomics Consortium: Lee PH, Anttila V, Won H, Feng YA, Rosenthal J, Zhu Z, Tucker-Drob EM, Nivard MG, Grotzinger AD, Posthuma D, Wang MM, Yu D, Stahl EA, …, …, Andlauer TFM, …, …, Smoller JW (2019): Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell 179(7):P1469-1482.e11 View abstract
Andlauer TFM, Guzman-Parra J, Streit F, Strohmaier J, González MJ, Gil Flores S, Cabaleiro Fabeiro FJ, del Río Noriega F, Perez Perez F, Haro González J, Orozco Diaz G, de Diego-Otero Y, Moreno-Kuestner B, Auburger G, Degenhardt F, Heilmann-Heimbach S, Herms S, Hoffmann P, Frank J, Foo JC, Treutlein J, Witt SH, Cichon C, Kogevinas M, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Rivas F, Mayoral F, Müller-Myhsok B, Forstner AJ, Nöthen MM, Rietschel M (2019): Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. Molecular Psychiatry 26:1286-1298 (2021) View abstract …or read the German press release
International Multiple Sclerosis Genetics Consortium: Patsopoulos NA, Baranzini SE, Santaniello A, Shoostari P, Cotsapas C, Wong G, Beecham AH, James T, Replogle J, Vlachos IS, McCabe C, Pers TH, Brandes A, White C, Keenan B, Cimpean M, Winn P, Panteliadis IP, Robbins A, Andlauer TFM, …, …, De Jager PL (2019): Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility. Science 365(6460):eaav7188 View abstract
Adorjan K, Mekonnen Z, Tessema F, Ayana M, Degenhardt F, Hoffmann P, Fricker N, Widmann M, Riedke H, Toennes S, Soboka M, Suleman S, Andlauer TFM, Tesfaye M, Rietschel M, Susser E, Odenwald M, Schulze TG, Mattheisen M (2019): Genotype-phenotype feasibility studies on khat abuse, traumatic experiences and psychosis in Ethiopia. Psychiatric Genetics 30(1):34-38 View abstract
Comes AL, Senner F, Budde M, Adorjan K, Anderson-Schmidt H, Andlauer TFM, Gade K, Hake M, Heilbronner U, Kalman JL, Reich-Erkelenz D, Klöhn-Saghatolislam F, Schaupp SK, Schulte EC, Juckel G, Dannlowski U, Schmauß M, Zimmermann J, Reimer J, Reininghaus E, Anghelescu IG, Arolt V, Baune BT, Konrad C, Thiel A, Fallgatter AJ, Nieratschker V, Figge C, von Hagen M, Koller M, Becker T, Wigand ME, Jäger M, Dietrich DE, Stierl S, Scherk H, Spitzer C, Folkerts H, Witt SH, Degenhardt F, Forstner AJ, Rietschel M, Nöthen MM, Wiltfang J, Falkai P, Schulze TG, Papiol S (2019): The genetic relationship between educational attainment and cognitive performance in major psychiatric disorders. Translational Psychiatry 9(1):210 View abstract
Glanville KP, Coleman JRI, Hanscombe KB, Euesden J, Choi SW, Purves KL, Breen G, Air TM, Andlauer TFM, Baune BT, Binder EB, Blackwood DHR, Boomsma DI, Buttenschøn HN, Colodro-Conde L, Dannlowski U, Direk N, Dunn EC, Forstner AJ, Geus EJd, Grabe HJ, Hamilton SP, Jones I, Jones LA, Knowles JA, Kutalik Z, Levinson DF, Lewis G, Lind PA, Lucae S, Magnusson PK, McGuffin P, McIntosh AM, Milaneschi Y, Mors O, Mostafavi S, Müller-Myhsok B, Pedersen NL, Penninx BW, Potash JB, Preisig M, Ripke S, Shi J, Shyn SI, Smoller JW, Streit F, Sullivan PF, Tiemeier H, Uher R, Auwera SVd, Weissman MM, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, O’Reilly PF, Lewis CM (2019): Classical HLA alleles and C4 haplotypes are not significantly associated with depression. Biological Psychiatry 87(5):419–430 View abstract
Paul R, Andlauer TFM, Czamara D, Hoehn D, Lucae S, Pütz B, Lewis CM, Uher R, Müller-Myhsok B, Ising M, Sämann PG (2019): Treatment response classes in major depressive disorder identified by model-based clustering and validated by clinical prediction models. Translational Psychiatry 9:187 View abstract
van der Lee SJ, Conway OJ, Jansen I, Carrasquillo MM, Kleineidam L, van den Akker E, Hernández I, van Eijk KR, Stringa N, Chen JA, Zettergren A, Andlauer TFM, Diez-Fairen M, Simon-Sanchez J, Lleó A, Zetterberg H, Nygaard M, Blauwendraat C, Savage JE, Mengel-From J, Moreno-Grau S, Wagner M, Fortea J, Keogh MJ, Blennow K, Skoog I, Friese MA, Pletnikova O, Zulaica M, Lage C, de Rojas I, Riedel-Heller S, Illán-Gala I, Wei W, Jeune B, Orellana A, Then Bergh F, Wang X, Hulsman M, Beker N, Tesi N, Morris CM, Indakoetxea B, Collij LE, Scherer M, Morenas-Rodríguez E, Ironside JW, van Berckel BNM, Alcolea D, Wiendl H, Strickland SL, Pastor P, Rodríguez Rodríguez E, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), Boeve BF, Petersen RC, Ferman TJ, van Gerpen JA, Reinders MJT, Uitti RJ, Tárraga L, Maier W, Dols-Icardo O, Kawalia A, Dalmasso MC, Boada M, Zettl UK, van Schoor NM, Beekman M, Allen M, Masliah E, de Munain AL, Pantelyat A, Wszolek ZK, Ross OA, Dickson DW, Graff-Radford NR, Knopman D, Rademakers R, Lemstra AW, Pijnenburg YAL, Scheltens P, Gasser T, Chinnery PF, Hemmer B, Huisman MA, Troncoso J, Moreno F, Nohr EA, Sørensen TIA, Heutink P, Sánchez-Juan P, Posthuma D; GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Clarimón J, Christensen K, Ertekin-Taner N, Scholz SW, Ramirez A, Ruiz A, Slagboom E, van der Flier WM, Holstege H (2019): A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity. Acta Neuropathologica 138(2):237-250 View abstract
International Multiple Sclerosis Genetics Consortium: Madireddy L, Patsopoulos NA, Cotsapas C, Bos SD, Beecham A, McCauley J, Kim K, Jia X, Santaniello A, Caillier SJ, Andlauer TFM, Barcellos LF, Berge T, Bernardinelli L, Martinelli-Boneschi F, Booth DR, Briggs F, Celius EG, Comabella M, Comi G, Cree BAC, D’Alfonso S, Dedham K, Duquette P, Efthimios D, Esposito F, Fontaine B, Gasperi C, Goris A, Dubois B, Gourraud PA, Hadjigeorgiou G, Haines J, Hawkins C, Hemmer B, Hintzen R, Horakova D, Isobe N, Kalra S, Kira JI, Khalil M, Kockum I, Lill CM, Lincoln MR, Luessi F, Martin R, Oturai A, Palotie A, Pericak-Vance MA, Henry R, Saarela J, Ivinson A, Olsson T, Taylor BV, Stewart GJ, Harbo HF, Compston A, Hauser SL, Hafler DA, Zipp F, De Jager P, Sawcer S, Oksenberg JR, Baranzini SE (2019): A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis. Nature Communications 10:2236 View abstract
Meller T, Schmitt S, Stein F, Brosch K, Mosebach J, Yüksel D, Zaremba D, Grotegerd D, Dohm K, Meinert S, Förster K, Redlich R, Opel N, Repple J, Hahn T, Jansen A, Andlauer TFM, Forstner AJ, Heilmann-Heimbach S, Streit F, Witt SH, Rietschel M, Müller-Myhsok B, Nöthen MM, Dannlowski U, Krug A, Kircher T, Nenadić I (2019): Associations of schizophrenia risk genes ZNF804A and CACNA1C with schizotypy and modulation of attention in healthy subjects. Schizophrenia Research 208:67-75. View abstract
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G (2019): Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry 9(1):77 View abstract
Anderson-Schmidt H, Gade K, Malzahn D, Papiol S, Budde M, Heilbronner U, Reich-Erkelenz D, Adorjan K, Kalman JL, Senner F, Comes AL, Flatau L, Gryaznova A, Hake M, Reitt M, Schmauß M, Juckel G, Reimer J, Zimmermann J, Figge C, Reininghaus E, Anghelescu IG, Konrad C, Thiel A, von Hagen M, Koller M, Stierl S, Scherk H, Spitzer C, Folkerts H, Becker T, Dietrich DE, Andlauer TFM, Degenhardt F, Nöthen MM, Witt SH, Rietschel M, Wiltfang J, Falkai P, Schulze TG (2019): The influence of religious activity and polygenic schizophrenia risk on religious delusions in schizophrenia. Schizophrenia Research 210, 255-261 View abstract
Six additional publications as part of the MDD Working Group of the Psychiatric Genomics Consortium:
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications 10:2548 View abstract
Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics 51, 431–444 View abstract
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Biological Psychiatry 88(2):169-184 View abstract
Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults: A 2-Sample Mendelian Randomization Study. JAMA Psychiatry 76(4):399-408 View abstract
Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180(1):35-45 View abstract
Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. Psychological Medicine 49(7):1218-1226 View abstract
2018
International Multiple Sclerosis Genetics Consortium: Mitrovič M, Patsopoulos NA, Beecham AH, Dankowski T, Goris A, Dubois B, D’hooghe MB, Lemmens R, Van Damme P, Søndergaard HB, Sellebjerg F, Sorensen PS, Ullum H, Thørner LW, Werge T, Saarela J, Cournu-Rebeix I, Damotte V, Fontaine B, Guillot-Noel L, Lathrop M, Vukusik S, Gourraud PA, Andlauer TFM, Pongratz V, Buck D, Gasperi C, Bayas A, Heesen C, Kümpfel T, Linker R, Paul F, Stangel M, Tackenberg B, Bergh FT, Warnke C, Wiendl H, Wildemann B, Zettl U, Ziemann U, Tumani H, Gold R, Grummel V, Hemmer B, Knier B, Lill CM, Luessi F, Dardiotis E, Agliardi C, Barizzone N, Mascia E, Bernardinelli L, Comi G, Cusi D, Esposito F, Ferrè L, Comi C, Galimberti D, Leone MA, Sorosina M, Mescheriakova J, Hintzen R, van Duijn C, Theunissen CE, Bos SD, Myhr KM, Celius EG, Lie BA, Spurkland A, Comabella M, Montalban X, Alfredsson L, Stridh P, Hillert J, Jagodic M, Piehl F, Jelčić I, Martin R, Sospedra M, Ban M, Hawkins C, Hysi P, Kalra S, Karpe F, Khadake J, Lachance G, Neville M, Santaniello A, Caillier SJ, Calabresi PA, Cree BAC, Cross A, Davis MF, Haines JL, de Bakker PIW, Delgado S, Dembele M, Edwards K, Fitzgerald KC, Hakonarson H, Konidari I, Lathi E, Manrique CP, Pericak-Vance MA, Piccio L, Schaefer C, McCabe C, Weiner H, Goldstein J, Olsson T, Hadjigeorgiou G, Taylor B, Tajouri L, Charlesworth J, Booth DR, Harbo HF, Ivinson AJ, Hauser SL, Compston A, Stewart G, Zipp F, Barcellos LF, Baranzini SE, Martinelli-Boneschi F, D’Alfonso S, Ziegler A, Oturai A, McCauley JL, Sawcer SJ, Oksenberg JR, De Jager PL, Kockum I, Hafler DA, Cotsapas C (2018): Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk Cell, 175(6):1679-87 View abstract
Maaser A, Forstner AJ, Strohmaier J, Hecker J, Ludwig KU, Sivalingam S, Streit F, Degenhardt F, Witt SH, Reinbold CS, Koller AC, Raff R, Heilmann-Heimbach S, Fischer SB, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Herms S, Hoffmann P, Thiele H, Nürnberg P, Löhlein Fier H, Orozco-Díaz G, Carmenate-Naranjo D, Proenza-Barzaga N, Auburger GWJ, Andlauer TFM, Cichon S, Marcheco-Teruel B, Mors O, Rietschel M, Nöthen MM (2018): Exome sequencing in large, multiplex bipolar disorder families from Cuba. PLOS ONE 13(10):e0205895. View abstract
Budde M, Anderson-Schmidt H, Gade K, Reich-Erkelenz D, Adorjan K, Kalman JL, Senner F, Papiol S, Andlauer TFM, Comes AL, Schulte EC, Klöhn-Saghatolislam F, Gryaznova A, Hake M, Bartholdi K, Flatau L, Reitt M, Quast S, Stegmaier S, Meyers M, Emons B, Haußleiter IS, Juckel G, Nieratschker V, Dannlowski U, Schaupp SK, Schmauß M, Zimmermann J, Reimer J, Schulz S, Wiltfang J, Reininghaus E, Anghelescu IG, Arolt V, Baune BT, Konrad C, Thiel A, Fallgatter AJ, Figge C, von Hagen M, Koller M, Lang FU, Wigand ME, Becker T, Jäger M, Dietrich DE, Stierl S, Scherk H, Spitzer C, Folkerts H, Witt SH, Degenhardt F, Forstner AJ, Rietschel M, Nöthen MM, Falkai P, Schulze TG, Heilbronner U (2018): A longitudinal approach to biological psychiatric research: The PsyCourse study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180(2):89-102. View abstract
Kalman JL, Papiol S, Forstner AJ, Heilbronner U, Degenhardt F, Strohmaier J, Adli M, Adorjan K, Akula N, Alda M, Anderson-Schmidt H, Andlauer TFM, Anghelescu IG, Ardau R, Arias B, Arolt V, Aubry JM, Backlund L, Bartholdi K, Bauer M, Baune BT, Becker T, Bellivier F, Benabarre A, Bengesser S, Bhattacharjee AK, Biernacka JM, Birner A, Brichant-Petitjean C, Budde M, Cervantes P, Chillotti C, Cichon S, Clark SR, Colom F, Comes AL, Cruceanu C, Czerski PM, Dannlowski U, Dayer A, Del Zompo M, DePaulo JR, Dietrich DE, Étain B, Ethofer T, Falkai P, Fallgatter A, Figge C, Flatau L, Folkerts H, Frisen L, Frye MA, Fullerton JM, Gade K, Gard S, Garnham JS, Goes FS, Grigoroiu-Serbanescu M, Gryaznova A, Hake M, Hauser J, Herms S, Hoffmann P, Hou L, Jäger M, Jamain S, Jiménez E, Juckel G, Kahn JP, Kassem L, Kelsoe J, Kittel-Schneider S, Kliwicki S, Klohn-Sagatholislam F, Koller M, König B, Konrad C, Lackner N, Laje G, Landén M, Lang FU, Lavebratt C, Leboyer M, Leckband SG, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McMahon FJ, Mitchell PB, Mitjans M, Mondimore FM, Monteleone P, Nieratschker V, Nievergelt CM, Novák T, Ösby U, Pfennig A, Potash JB, Reich-Erkelenz D, Reif A, Reimer J, Reininghaus E, Reitt M, Ripke S, Rouleau GA, Rybakowski JK, Schalling M, Scherk H, Schmauß M, Schofield PR, Schubert KO, Schulte EC, Schulz S, Senner F, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Spitzer C, Squassina A, Stamm T, Stegmaier S, Stierl S, Stopkova P, Thiel A, Tighe SK, Tortorella A, Turecki G, Vieta E, Veeh J, von Hagen M, Wigand ME, Wiltfang J, Witt S, Wright A, Zandi PP, Zimmermann J, Nöthen M, Rietschel M, Schulze TG (2018): Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. Bipolar Disorders 21(1):68-75 View abstract
Brainstorm Consortium: Anttila V, Bulik-Sullivan B, Finucane HK, …, …, Andlauer TFM, …, …, Grigoroiu-Serbanescu M, Edenberg HJ, Murray R (2018): Analysis of shared heritability in common disorders of the brain Science 360(6395):eaap8757 View abstract
Kular L, Liu Y, Ruhrmann S, Zheleznyakova G, Marabita F, Gomez-Cabrero D, James T, Ewing E, Lindén M, Górnikiewicz B, Aeinehband S, Stridh P, Link J, Andlauer TFM, Gasperi C, Wiendl H, Zipp F, Gold R, Tackenberg B, Weber F, Hemmer B, Strauch K, Heilmann-Heimbach S, Rawal R, Schminke U, Schmidt CO, Kacprowski T, Franke A, Laudes M, Dilthey AT, Celius EG, Søndergaard HB, Tegnér J, Harbo HF, Oturai AB, Olafsson S, Eggertsson HP, Halldorsson BV, Hjaltason H, Olafsson E, Jonsdottir I, Stefansson K, Olsson T, Piehl F, Ekström TJ, Kockum I, Feinberg AP, Jagodic M (2018): DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis. Nature Communications 9(1):2397 View abstract
Andlauer TFM, Müller-Myhsok B, Ripke S (2018): Statistical genetics: Genome-wide studies. Chapter 4 in: Psychiatric Genetics – A Primer for Clinical and Basic Scientists Editors: T. Schulze and F. McMahon Oxford University Press; doi:10.1093/med/9780190221973.003.0004. View abstract
Fulterer A*, Andlauer TFM*, Ender A*, Maglione M* (shared first), Eyring K, Woitkuhn J, Lehmann M, Matkovic-Rachid T, Geiger JRP, Walter AM, Nagel KI, Sigrist SJ (2018): Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses Cell Reports 23(5):1259-74 View abstract
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium: Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TFM, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, Blackwood DRH, Bryois J, Buttenschøn HN, Bybjerg-Grauholm J, Cai N, Castelao E, Christensen JH, Clarke TK, Coleman JIR, Colodro-Conde L, Couvy-Duchesne B, Craddock N, Crawford GE, Crowley CA, Dashti HS, Davies G, Deary IJ, Degenhardt F, Derks EM, Direk N, Dolan CV, Dunn EC, Eley TC, Eriksson N, Escott-Price V, Kiadeh FHF, Finucane HK, Forstner AJ, Frank J, Gaspar HA, Gill M, Giusti-Rodríguez P, Goes FS, Gordon SD, Grove J, Hall LS, Hannon E, Hansen CS, Hansen TF, Herms S, Hickie IB, Hoffmann P, Homuth G, Horn C, Hottenga JJ, Hougaard DM, Hu M, Hyde CL, Ising M, Jansen R, Jin F, Jorgenson E, Knowles JA, Kohane IS, Kraft J, Kretzschmar WW, Krogh J, Kutalik Z, Lane JM, Li Y, Li Y, Lind PA, Liu X, Lu L, MacIntyre DJ, MacKinnon DF, Maier RM, Maier W, Marchini J, Mbarek H, McGrath P, McGuffin P, Medland SE, Mehta D, Middeldorp CM, Mihailov E, Milaneschi Y, Milani L, Mill J, Mondimore FM, Montgomery GW, Mostafavi S, Mullins N, Nauck M, Ng B, Nivard MG, Nyholt DR, O’Reilly PF, Oskarsson H, Owen MJ, Painter JN, Pedersen CB, Pedersen MG, Peterson RE, Pettersson E, Peyrot WJ, Pistis G, Posthuma D, Purcell SM, Quiroz JA, Qvist P, Rice JP, Riley BP, Rivera M, Saeed Mirza S, Saxena R, Schoevers R, Schulte EC, Shen L, Shi J, Shyn SI, Sigurdsson E, Sinnamon GBC, Smit JH, Smith DJ, Stefansson H, Steinberg S, Stockmeier CA, Streit F, Strohmaier J, Tansey KE, Teismann H, Teumer A, Thompson W, Thomson PA, Thorgeirsson TE, Tian C, Traylor M, Treutlein J, Trubetskoy V, Uitterlinden AG, Umbricht D, Van der Auwera S, van Hemert AM, Viktorin A, Visscher PM, Wang Y, Webb BT, Weinsheimer SM, Wellmann J, Willemsen G, Witt SH, Wu Y, Xi HS, Yang J, Zhang F; eQTLGen; 23andMe, Arolt V, Baune BT, Berger K, Boomsma DI, Cichon S, Dannlowski U, de Geus ECJ, DePaulo JR, Domenici E, Domschke K, Esko T, Grabe HJ, Hamilton SP, Hayward C, Heath AC, Hinds DA, Kendler KS, Kloiber S, Lewis G, Li QS, Lucae S, Madden PFA, Magnusson PK, Martin NG, McIntosh AM, Metspalu A, Mors O, Mortensen PB, Müller-Myhsok B, Nordentoft M, Nöthen MM, O’Donovan MC, Paciga SA, Pedersen NL, Penninx BWJH, Perlis RH, Porteous DJ, Potash JB, Preisig M, Rietschel M, Schaefer C, Schulze TG, Smoller JW, Stefansson K, Tiemeier H, Uher R, Völzke H, Weissman MM, Werge T, Winslow AR, Lewis CM, Levinson DF, Breen G, Børglum AD, Sullivan PF; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2018): Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression Nature Genetics 50(5):668-681 View abstract
Buck D*, Andlauer TFM*(shared first), Igl W, Wicklein E-M, Mühlau M, Weber F, Köchert K, Pohl C, Arnason B, Comi G, Cook S, Filippi M, Hartung H-P, Jeffery D, Kappos L, Barkhof F, Edan G, Freedman MS, Montalban X, Müller-Myhsok B, Hemmer B, The BEYOND and BENEFIT Study Groups (2018): Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials Multiple Sclerosis Journal 25(4):565-573 View abstract
Three additional publications as part of the MDD Working Group of the Psychiatric Genomics Consortium:
Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder PLOS ONE 13(12):e0209160 View abstract
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder Communications Biology 1:163 View abstract
Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 4(1):91-100 View abstract
2017
Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TFM, Beekman AT, Berger K, Blackwood DH, Boomsma DI, Breen G, Buttenschøn HN, Byrne EM, Cichon S, Clarke TK, Couvy-Duchesne B, Craddock N, de Geus EJ, Degenhardt F, Dunn EC, Edwards AC, Fanous AH, Forstner AJ, Frank J, Gill M, Gordon SD, Grabe HJ, Hamilton SP, Hardiman O, Hayward C, Heath AC, Henders AK, Herms S, Hickie IB, Hoffmann P, Homuth G, Hottenga JJ, Ising M, Jansen R, Kloiber S, Knowles JA, Lang M, Li QS, Lucae S, MacIntyre DJ, Madden PA, Martin NG, McGrath PJ, McGuffin P, McIntosh AM, Medland SE, Mehta D, Middeldorp CM, Milaneschi Y, Montgomery GW, Mors O, Müller-Myhsok B, Nauck M, Nyholt DR, Nöthen MM, Owen MJ, Penninx BW, Pergadia ML, Perlis RH, Peyrot WJ, Porteous DJ, Potash JB, Rice JP, Rietschel M, Riley BP, Rivera M, Schoevers R, Schulze TG, Shi J, Shyn SI, Smit JH, Smoller JW, Streit F, Strohmaier J, Teumer A, Treutlein J, Van der Auwera S, van Grootheest G, van Hemert AM, Völzke H, Webb BT, Weissman MM, Wellmann J, Willemsen G, Witt SH, Levinson DF, Lewis CM, Wray NR, Flint J, Sullivan PF, Kendler KS (2017): Genetic effects influencing risk for major depressive disorder in China and Europe Translational Psychiatry 7(3):e1074 View abstract
Three additional publications as part of the MDD Working Group of the Psychiatric Genomics Consortium:
Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations JAMA Psychiatry 74(12):1214-1225 View abstract
Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes Scientific Reports 7(1):15351 View abstract
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium Biological Psychiatry 4(2):138-147 View abstract
2016
Mühlau M, Andlauer TFM, Hemmer B (2016): HLA Genetic Risk Burden in Multiple Sclerosis JAMA Neurology 73(12):1500-1501 View abstract
Gupta VK, Pech U, Bhukel A, Fulterer A, Ender A, Mauermann SF, Andlauer TFM, Antwi-Adjei E, Beuschel C, Thriene K, Maglione M, Quentin C, Bushow R, Schwärzel M, Mielke T, Madeo F, Dengjel J, Fiala A, Sigrist SJ (2016): Spermidine Suppresses Age-Associated Memory Impairment by Preventing Adverse Increase of Presynaptic Active Zone Size and Release PLoS Biology 14(9):e1002563 View abstract
Schirmer L, Worthington V, Solloch U, Loleit V, Grummel V, Lakdawala N, Grant D, Wassmuth R, Schmidt AH, Gebhardt F, Andlauer TFM, Sauter J, Berthele A, Lunn MP, Hemmer B (2016): Higher frequencies of HLA DQB1*05:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain-Barré syndrome Journal of Neurology 263(10):2105-13 View abstract
Andlauer TFM, Buck D, Antony G, Bayas A, Bechmann L, Berthele A, Chan A, Gasperi C, Gold R, Graetz C, Haas J, Hecker M, Infante-Duarte C, Knop M, Kümpfel T, Limmroth V, Linker RA, Loleit V, Luessi F, Meuth SG, Mühlau M, Nischwitz S, Paul F, Pütz M, Ruck T, Salmen A, Stangel M, Stellmann JP, Stürner KH, Tackenberg B, Then Bergh F, Tumani H, Warnke C, Weber F, Wiendl H, Wildemann B, Zettl UK, Ziemann U, Zipp F, Arloth J, Weber P, Radivojkov-Blagojevic M, Scheinhardt MO, Dankowski T, Bettecken T, Lichtner P, Czamara D, Carrillo-Roa T, Binder EB, Berger K, Bertram L, Franke A, Gieger C, Herms S, Homuth G, Ising M, Jöckel KH, Kacprowski T, Kloiber S, Laudes M, Lieb W, Lill CM, Lucae S, Meitinger T, Moebus S, Müller-Nurasyid M, Nöthen MM, Petersmann A, Rawal R, Schminke U, Strauch K, Völzke H, Waldenberger M, Wellmann J, Porcu E, Mulas A, Pitzalis M, Sidore C, Zara I, Cucca F, Zoledziewska M, Ziegler A, Hemmer B, Müller-Myhsok B (2016): Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation Science Advances 2(6) e1501678 View abstract …or read the press release
2015
Dankowski T, Buck D, Andlauer TFM, Antony G, Bayas A, Bechmann L, Berthele A, Bettecken T, Chan A, Franke A, Gold R, Graetz C, Haas J, Hecker M, Herms S, Infante-Duarte C, Jöckel KH, Kieseier BC, Knier B, Knop M, Kümpfel T, Lichtner P, Lieb W, Lill CM, Limmroth V, Linker RA, Loleit V, Meuth SG, Moebus S, Müller-Myhsok B, Nischwitz S, Nöthen MM, Paul F, Pütz M, Ruck T, Salmen A, Stangel M, Stellmann JP, Strauch K, Stürner KH, Tackenberg B, Then Bergh F, Tumani H, Waldenberger M, Weber F, Wiendl H, Wildemann B, Zettl UK, Ziemann U, Zipp F, Hemmer B, Ziegler A; German Competence Network for Multiple Sclerosis (KKNMS) (2015): Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array Genetic Epidemiology 39(8):601-8 View abstract
Beck K, Ehmann N, Andlauer TFM, Ljaschenko D, Strecker K, Fischer M, Kittel RJ, Raabe T (2015): Loss of the Coffin-Lowry syndrome-associated gene RSK2 alters ERK activity, synaptic function and axonal transport in Drosophila motoneurons Disease Models & Mechanisms 8(11):1389-400 View abstract
Siebert M, Böhme MA, Driller JH, Babikir H, Mampell MM, Rey U, Ramesh N, Matkovic T, Holton N, Reddy-Alla S, Göttfert F, Kamin D, Quentin C, Klinedinst S, Andlauer TFM, Hell SW, Collins CA, Wahl MC, Loll B, Sigrist SJ (2015): A high affinity RIM-binding protein/Aplip1 interaction prevents the formation of ectopic axonal active zones eLife 4.e06935 View abstract
Nischwitz S, Wolf C, Andlauer TFM, Czamara D, Zettl UK, Rieckmann P, Buck D, Ising M, Bettecken T, Mueller-Myhsok B, Weber F (2015) MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. Journal of Neuroimmunology 279:46-9 View abstract
2014
Andlauer TFM, Scholz-Kornehl S, Tian R, Kirchner M, Babikir HA, Depner H, Loll B, Quentin C, Gupta VK, Holt MG, Dipt S, Cressy M, Wahl MC, Fiala A, Selbach M, Schwärzel M, Sigrist SJ (2014): Drep-2 is a novel synaptic protein important for learning and memory eLife 3.e03895 View abstract …or read the press release
2013
Andlauer TFM (2013): Structural and Functional Diversity of Synapses in the Drosophila CNS Doctoral thesis, Graduate School of Life Sciences, Julius-Maximilians-Universität Würzburg Download at OPUS
2012
Andlauer TFM, Sigrist SJ (2012): In vivo imaging of Drosophila larval neuromuscular junctions to study synapse assembly. Cold Spring Harbor Protocols 2012(4):407-13 View abstract (Reissue of a protocol published in Andlauer TFM & Sigrist SJ, 2010)
Andlauer TFM, Sigrist SJ (2012): Building an imaging chamber for in vivo imaging of Drosophila larvae. Cold Spring Harbor Protocols 2012(4):476-80 View abstract (Reissue of a protocol published in Andlauer TFM & Sigrist SJ, 2010)
Andlauer TFM, Sigrist SJ (2012): In vivo imaging of the Drosophila larval neuromuscular junction. Cold Spring Harbor Protocols 2012(4):481-9 View abstract (Reissue of a protocol published in Andlauer TFM & Sigrist SJ, 2010)
Andlauer TFM, Sigrist SJ (2012): Quantitative analysis of Drosophila larval neuromuscular junction morphology. Cold Spring Harbor Protocols 2012(4):490-3 View abstract (Reissue of a protocol published in Andlauer TFM & Sigrist SJ, 2010)
2011
NMJ image on the cover page of the Neuroforum journal issue 2011/4 In addition, images in: Wichmann C, Sigrist SJ (2011): Dem Innenleben der Synapsen auf der Spur. Neuroforum 11(4):144-51 Download as pdf or visit the Neuroforum-Homepage
Park B, Alves CH, Lundvig DM, Tanimoto N, Beck SC, Huber G, Richard F, Klooster J, Andlauer TFM, Swindell EC, Jamrich M, Le Bivic A, Seeliger MW, Wijnholds J. (2011): PALS1 is essential for retinal pigment epithelium structure and neural retina stratification. Journal of Neuroscience 31(47):17230-41 View abstract
Waites CL, Leal-Ortiz SA, Andlauer TFM, Sigrist SJ, Garner CC (2011): Piccolo regulates the dynamic assembly of presynaptic f-actin. Journal of Neuroscience 31(40):14250-63 View abstract
Christiansen F, Zube C, Andlauer TFM, Wichmann C, Fouquet W, Owald D, Mertel S, Leiss F, Tavosanis G, Farca Luna AJ, Fiala A, Sigrist SJ (2011): Presynapses in Kenyon Cell Dendrites in the Mushroom Body Calyx of Drosophila. Journal of Neuroscience 31(26):9696-9707 View abstract
Sigrist SJ, Andlauer TFM (2011): Fighting the famine with an amine: synaptic strategies for smart search. Nature Neuroscience 14(2):124-6 View abstract
2010
Kremer MC, Christiansen F, Leiss F, Paehler M, Knapek S, Andlauer TFM, Förstner F, Kloppenburg P, Sigrist SJ, Tavosanis G (2010): Structural Long-Term Changes at Mushroom Body Input Synapses. Current Biology 20(21):1938-44 View abstract
Andlauer TFM, Sigrist SJ (2010): In Vivo Imaging of Drosophila Larval Neuromuscular Junctions to Study Synapse Assembly. Chapter 21 in: Drosophila Neurobiology, B. Zhang, M.R. Freeman, and S. Waddell, eds. (Cold Spring Harbor Press) View abstract
Fischbach KF, Linneweber GA, Andlauer TFM, Hertenstein A, Bonengel B, Chaudhary K (2009): The irre cell recognition module (IRM) proteins. Journal of Neurogenetics 21(1-2):48-67 View abstract
2008
MARCM images in: Fischbach KF, Hiesinger PR (2008): Optic lobe development. Advances in Experimental Medicine and Biology 628:115-36 View abstract
2007
Andlauer TFM (2007): Rst und kirre exprimierende Zelltypen im optischen Lobus von D. melanogaster Diplomarbeit, Fakultät für Biologie der Albert-Ludwigs-Universität Freiburg im Breisgau Download as pdf
2006
Contributed experiments to: Odegrip R, Nilsson AS, Haggård-Ljungquist E. (2006): Identification of a gene encoding a functional reverse transcriptase within a highly variable locus in the P2-like coliphages. Journal of Bacteriology 188(4):1643-7 View abstract
