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Alle Publikationen des Instituts finden Sie in der linken Leiste nach Veröffentlichungsjahr sortiert bzw. gruppiert.
Ausgewählte Publikationen ab 2020
- Byun J, Han Y, Li Y, Xia J, Long E, Choi J, Xiao X, Zhu M, Zhou W, Sun R, Bossé Y, Song Z, Schwartz A, Lusk C, Rafnar T, Stefansson K, Zhang T, Zhao W, Pettit RW, Liu Y, Li X, Zhou H, Walsh KM, Gorlov I, Gorlova O, Zhu D, Rosenberg SM, Pinney S, Bailey-Wilson JE, Mandal D, de Andrade M, Gaba C, Willey JC, You M, Anderson M, Wiencke JK, Albanes D, Lam S, Tardon A, Chen C, Goodman G, Bojeson S, Brenner H, Landi MT, Chanock SJ, Johansson M, Muley T, Risch A, Wichmann HE, Bickeböller H, Christiani DC, Rennert G, Arnold S, Field JK, Shete S, Le Marchand L, Melander O, Brunnstrom H, Liu G, Andrew AS, Kiemeney LA, Shen H, Zienolddiny S, Grankvist K, Johansson M, Caporaso N, Cox A, Hong YC, Yuan JM, Lazarus P, Schabath MB, Aldrich MC, Patel A, Lan Q, Rothman N, Taylor F, Kachuri L, Witte JS, Sakoda LC, Spitz M, Brennan P, Lin X, McKay J, Hung RJ, Amos CI (2022) Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. NAT GENET 54(8): 1167, doi: 10.1038/s41588-022-01115-x
- Rosenberger A, Muttray N, Hung RJ, Christiani DC, Caporaso NE, Liu G, Bojesen SE, Le Marchand L, Albanes D, Aldrich MC, Tardon A, Fernández-Tardón G, Rennert G, Field JK, Davies MPA, Liloglou T, Kiemeney LA, Lazarus P, Wendel B, Haugen A, Zienolddiny S, Lam S, Schabath MB, Andrew AS, Duell EJ, Arnold SM, Goodman GE, Chen C, Doherty JA, Taylor F, Cox A, Woll PJ, Risch A, Muley TR, Johansson M, Brennan P, Landi MT, Shete SS, Amos CI, Bickeböller H, INTEGRAL-ILCCO Consortium (2022) Gene-gene interaction of AhRwith and within the Wntcascade affects susceptibility to lung cancer. EUR J MED RES 27(1): 14, doi: 10.1186/s40001-022-00638-7
- Rosenberger A, Tozzi V, Bickeböller H, INTEGRAL-ILCCO consortium (2022) Iam hiQ-a novel pair of accuracy indices for imputed genotypes. BMC BIOINFORMATICS 23(1): 50, doi: 10.1186/s12859-022-04568-3
- Stahl K, Adorjan K, Anderson-Schmidt H, Budde M, Comes AL, Gade K, Heilbronner M, Kalman JL, Klöhn-Saghatolislam F, Oraki Kohshour M, Papiol S, Reich-Erkelenz D, Schaupp SK, Schulte EC, Senner F, Vogl T, Wiltfang J, Reininghaus E, Falkai P, Schulze TG, Bickeböller H, Heilbronner U (2022) Stability over time of scores on psychiatric rating scales, questionnaires and cognitive tests in healthy controls. BJPSYCH OPEN 8(2): e55, doi: 10.1192/bjo.2022.17
- Wendel B, Heidenreich M, Budde M, Heilbronner M, Oraki Kohshour M, Papiol S, Falkai P, Schulze TG, Heilbronner U, Bickeböller H (2022) Kalpra: A kernel approach for longitudinal pathway regression analysis integrating network information with an application to the longitudinal PsyCourse Study. FRONT GENET 13: 1015885, doi: 10.3389/fgene.2022.1015885
- Hung RJ, Warkentin MT, Brhane Y, Chatterjee N, Christiani DC, Landi MT, Caporaso NE, Liu G, Johansson M, Albanes D, Le Marchand L, Tardon A, Rennert G, Bojesen SE, Chen C, Field JK, Kiemeney LA, Lazarus P, Zienolddiny S, Lam S, Andrew AS, Arnold SM, Aldrich MC, Bickeböller H, Risch A, Schabath MB, McKay JD, Brennan P, Amos CI (2021) Assessing Lung Cancer Absolute Risk Trajectory based on a Polygenic Risk Model. CANCER RES 2021 Mar 15;81(6):1607-1615, doi: 10.1158/0008-5472.CAN-20-1237
- Sun R, Xu M, Li X, Gaynor S, Zhou H, Li Z, Bossé Y, Lam S, Tsao MS, Tardon A, Chen C, Doherty J, Goodman G, Bojesen SE, Landi MT, Johansson M, Field JK, Bickeböller H, Wichmann HE, Risch A, Rennert G, Arnold S, Wu X, Melander O, Brunnström H, Le Marchand L, Liu G, Andrew A, Duell E, Kiemeney LA, Shen H, Haugen A, Johansson M, Grankvist K, Caporaso N, Woll P, Dawn Teare M, Scelo G, Hong YC, Yuan JM, Lazarus P, Schabath MB, Aldrich MC, Albanes D, Mak R, Barbie D, Brennan P, Hung RJ, Amos CI, Christiani DC, Lin X (2021) Integration of multiomic annotation data to prioritize and characterize inflammation and immune-related risk variants in squamous cell lung cancer. GENET EPIDEMIOL 45(1): 99-114, doi: 10.1002/gepi.22358
- 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. TRANSL PSYCHIAT 11(1): 386, doi: 10.1038/s41398-021-01510-8
- Stahl K, Gola D, König IR (2021) Assessment of Imputation Quality: Comparison of Phasing and Imputation Algorithms in Real Data. FRONT GENET 2021 Sep 22;12:724037, DOI: 10.3389/fgene.2021.724037
- Kachuri L, Johansson M, Rashkin SR, Graff RE, Bossé Y, Manem V, Caporaso NE, Landi MT, Christiani DC, Vineis P, Liu G, Scelo G, Zaridz e D, Shete SS, Albanes D, Aldrich MC, Tardón A, Rennert G, Chen C, Goodman GE, Doherty JA, Bickeböller H, Field JK, Davies MP, Dawn Teare M, Kiemeney LA, Bojesen SE, Haugen A, Zienolddiny S, Lam S, Le Marchand L, Cheng I, Schabath MB, Duell EJ, Andrew AS, Manjer J, Lazarus P, Arnold S, McKay JD, Emami NC, Warkentin MT, Brhane Y, Obeidat M, Martin RM, Relton C, Davey Smith G, Haycock PC, Amos CI, Brennan P, Witte JS, Hung RJ (2020) Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility. NAT COMMUN 11(1): 27, doi: 10.1038/s41467-019-13855-2
- Partanen J, Hyvärinen K, Bickeböller H, Bogunia-Kubik K, Crossland RE, Ivanova M, Perutelli F, Dressel R (2020) Review of Genetic Variation as a Predictive Biomarker for Chronic Graft-Versus-Host-Disease After Allogeneic Stem Cell Transplantation. FRONT IMMUNOL 11: 575492, doi: 10.3389/fimmu.2020.575492
Ausgewählte Publikationen bis 2019 inklusive
- Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, Forstner AJ, Frank J, Gershon ES, Goes FS, Greenwood TA, Guo Y, Hipolito M, Hood L, Keating BJ, Koller DL, Lawson WB, Liu C, Mahon PB, McInnis MG, McMahon FJ, Meier SM, Mühleisen TW, Murray SS, Nievergelt CM, Nurnberger JI, Nwulia EA, Potash JB, Quarless D, Rice J, Roach JC, Scheftner WA, Schork NJ, Shekhtman T, Shilling PD, Smith EN, Streit F, Strohmaier J, Szelinger S, Treutlein J, Witt SH, Zandi PP, Zhang P, Zöllner S, Bickeböller H, Falkai PG, Kelsoe JR, Nöthen MM, Rietschel M, Schulze TG, Malzahn D (2019) Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. EUR NEUROPSYCHOPHARM 29(1): 156-170, doi: 10.1016/j.euroneuro.2018.10.005
- McKay JD, Hung RJ, Han Y, Zong X, Carreras-Torres R, Christiani DC, Caporaso NE, Johansson M, Xiao X, Li Y, Byun J, Dunning A, Pooley KA, Qian DC, Ji X, Liu G, Timofeeva MN, Bojesen SE, Wu X, Le Marchand L, Albanes D, Bickeböller H, Aldrich MC, Bush WS, Tardon A, Rennert G, Teare MD, Field JK, Kiemeney LA, Lazarus P, Haugen A, Lam S, Schabath MB, Andrew AS, Shen H, Hong YC, Yuan JM, Bertazzi PA, Pesatori AC, Ye Y, Diao N, Su L, Zhang R, Brhane Y, Leighl N, Johansen JS, Mellemgaard A, Saliba W, Haiman CA, Wilkens LR, Fernandez-Somoano A, Fernandez-Tardon G, van der Heijden HFM, Kim JH, Dai J, Hu Z, Davies MPA, Marcus MW, Brunnström H, Manjer J, Melander O, Muller DC, Overvad K, Trichopoulou A, Tumino R, Doherty JA, Barnett MP, Chen C, Goodman GE, Cox A, Taylor F, Woll P, Brüske I, Wichmann HE, Manz J, Muley TR, Risch A, Rosenberger A, Grankvist K, Johansson M, Shepherd FA, Tsao MS, Arnold SM, Haura EB, Bolca C, Holcatova I, Janout V, Kontic M, Lissowska J, Mukeria A, Ognjanovic S, Orlowski TM, Scelo G, Swiatkowska B, Zaridze D, Bakke P, Skaug V, Zienolddiny S, Duell EJ, Butler LM, Koh WP, Gao YT, Houlston RS, McLaughlin J, Stevens VL, Joubert P, Lamontagne M, Nickle DC, Obeidat M, Timens W, Zhu B, Song L, Kachuri L, Artigas MS, Tobin MD, Wain LV, SpiroMeta Consortium, Rafnar T, Thorgeirsson TE, Reginsson GW, Stefansson K, Hancock DB, Bierut LJ, Spitz MR, Gaddis NC, Lutz SM, Gu F, Johnson EO, Kamal A, Pikielny C, Zhu D, Lindströem S, Jiang X, Tyndale RF, Chenevix-Trench G, Beesley J, Bossé Y, Chanock S, Brennan P, Landi MT, Amos CI (2017) Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. NAT GENET 49(7): 1126-1132, doi: 10.1038/ng.3892
- Friedrichs S, Manitz J, Burger P, Amos CI, Risch A, Chang-Claude J, Wichmann HE, Kneib T, Bickeböller H, Hofner B (2017) Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies. COMPUT MATH METHOD M 2017: 6742763, doi: 10.1155/2017/6742763
- Papiol S, Popovic D, Keeser D, Hasan A, Schneider-Axmann T, Degenhardt F, Rossner M J, Bickeböller H, Schmitt A, Falkai P, and Malchow B (2017) Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia. Transl Psychiatry (2017) 7, e1159; doi:10.1038/tp.2017.131
- Rosenberger A, Sohns M, Friedrichs S, Hung RJ, Fehringer G, McLaughlin J, Amos CI, Brennan P, Risch A, Brüske I, Caporaso NE, Landi MT, Christiani DC, Wei Y, Bickeböller H (2017) Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus. PLOS ONE 12(3): e0173339, doi: 10.1371/journal.pone.0173339
- Pearce KF, Balavarca Y, Norden J, Jackson G, Holler E, Dressel R, Greinix H, Toubert A, Gluckman E, Hromadnikova I, Sedlacek P, Wolff D, Holtick U, Bickeböller H, Dickinson AM (2016) Impact of genomic risk factors on survival after haematopoietic stem cell transplantation for patients with acute leukaemia. INT J IMMUNOGENET 43(6): 404-412, doi: 10.1111/iji.12295
- Bickeböller H, Bailey JN, Beyene J, Cantor RM, Cordell HJ, Culverhouse RC, Engelman CD, Fardo DW, Ghosh S, König IR, Bermejo JL, Melton PE, Santorico SA, Satten GA, Sun L, Tintle NL, Ziegler A, MacCluer JW, Almasy L (2014). Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees. BMC Proceedings 2014, 8(Suppl 1):S1 (17 June 2014)
- Ha NT, Freytag S, Bickeböller H (2014) Coverage and efficiency in current SNP chips. EUR J HUM GENET, doi:10.1038/ejhg.2013.304
- Freytag S, Manitz J, Schlather M, Kneib T, Amos CI, Risch A, Chang-Claude J, Heinrich J, Bickeböller H (2013) A network-based kernel machine test for the identification of risk pathways in genome-wide association studies. HUM HERED, 76(2): 64-75.
- Sohns M, Viktorova E, Amos CI, Brennan P, Fehringer G, Gaborieau V, Han Y, Heinrich J, Chang-Claude J, Hung RJ, Müller-Nurasyid M, Risch A, Lewinger JP, Thomas DC, Bickeböller H (2013) Empirical Hierarchical Bayes Approach to Gene-Environment Interactions: Development and Application to Genome-Wide Association Studies of Lung Cancer in TRICL. GENET EPIDEMIOL, 37(6): 551-9.
- Bickeböller H (2022) Genetisch-molekulare Grundlagen von Gesundheit und Krankheit. In: Haring R. (eds) Gesundheitswissenschaften. Springer Reference Pflege – Therapie – Gesundheit. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-54179-1_6-2
- Bickeböller H, Thomas DC (2014), III.14. Statistical Methods in Genetic Epidemiology in "Handbook of Epidemiology" in Pigeot I, Ahrens W (Hrsg.), "Handbook of Epidemiology", Springer, 2nd edition, Pgs 1447 – 1480, ISBN-13: 978-0387098333
- Bickeböller H, Fischer C (2007), Einführung in die Genetische Epidemiologie, Lehrbuch (344 S.), Springer: Heidelberg
