Publications

2019

  • 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), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease 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, https://doi.org/10.1007/s00401-019-02026-8
    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 a
    ttention in healthy subjects.
    Schizophrenia Research 7 May 2019.
    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 9:77
    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 2019 Jan 3; https://doi.org/10.1016/j.schres.2018.12.025.
    View abstract at Pubmed
  • Two 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 at Pubmed
    • Identification of common genetic risk variants for autism spectrum disorder.
      Nature Genetics 51, 431–444
      View abstract at Pubmed

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 at Cell
  • 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 2018 Oct 31;13(10):e0205895.
    View abstract at Pubmed
  • 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 2018 Aug 2. doi: 10.1002/ajmg.b.32639.
    View abstract at Pubmed
  • 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 at Pubmed
  • 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 at Pubmed
  • 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 at Oxford University Press
  • 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 at Cell Reports
  • 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 at Pubmed
  • 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 at Pubmed
  • Four 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 2018 Dec 20;13(12):e0209160
      View abstract at Pubmed
    • Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder.
      Commun Biol. 2018 Oct 8;1:163
      View abstract at Pubmed
    • Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank
      Biol Psychiatry Cogn Neurosci Neuroimaging. 2018 Jul 31. S2451-9022(18)30181-2
      View abstract at Pubmed
    • Brainstorm Consortium (2018):
      Analysis of shared heritability in common disorders of the brain
      Science 360(6395), eaap8757, doi: 10.1126/science.aap8757.
      View abstract at Pubmed

2017

  • Four 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
      View abstract at Pubmed
    • Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes
      View abstract at Pubmed
    • Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium
      View abstract at Pubmed
    • Genetic effects influencing risk for major depressive disorder in China and Europe
      View abstract at Pubmed

2016

  • Mühlau M, Andlauer TFM, Hemmer B (2016):
    HLA Genetic Risk Burden in Multiple Sclerosis
    JAMA Neurology 73(12):1500-1501
    View abstract at Pubmed
  • 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 at Pubmed
  • 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 at Pubmed
  • 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 at Science Advances
    …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 at Pubmed
  • 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 at Pubmed
  • 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 at Pubmed
  • 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 at Pubmed

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 at eLife
    …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 at Pubmed
    (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 at Pubmed
    (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 at Pubmed
    (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 at Pubmed
    (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 at Pubmed
  • 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 at Pubmed
  • 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 at Pubmed
  • Sigrist SJ, Andlauer TFM (2011):
    Fighting the famine with an amine: synaptic strategies for smart search.
    Nature Neuroscience 14(2):124-6
    View abstract at Pubmed

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 at Pubmed
  • 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 at CSHL Press

2009

  • Andlauer TFM, Sigrist SJ (2009):
    Intravitale Bildgebung in Drosophila-Larven. Biospektrum 6/2009:632-635
    Download the pdf-file
    or visit the
    BIOspektrum-Homepage
  • 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 at Pubmed

2008

  • MARCM images in:
    Fischbach KF, Hiesinger PR (2008):
    Optic lobe development.
    Adv Exp Med Biol. 628:115-36
    View abstract at Pubmed

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.
    J Bacteriol. 188(4):1643-7
    View abstract at Pubmed