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Anders D. Børglum

center for genomics and personalized medicine

101H指数
703论文数
5.9W被引数
收录论文 326
发表时间
A novel method to disentangle tightly linked risk and resilience genes for brain disorders: application to Alzheimer’s disease一种解耦紧密关联的脑部疾病风险与抗性基因的新方法:在阿尔茨海默病中的应用
err2026-08-12
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PREAI
errEric J. Barnett; Jonathan L. Hess; Jiahui Hou; Valentina Escott-Price; Christine Fennema-Notestine; William Kremen; Shu-Ju Lin; Chunling Zhang; Ditte Demontis; Anders D. Børglum; Chris Gaiteri; Jeremy Elman; Peter Holmans; Stephen V. Faraone; Stephen J. Glatt
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Common and rare variant contributions to discontinuation of stimulant treatment in ADHD常见和罕见变异对ADHD兴奋剂治疗中断的贡献
err2026-02-28
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errOAAI
errJanne Pia Thirstrup; Jinjie Duan; Marta Ribases Haro; Maria Soler Artigas; Clara Albiñana; Søren Dalsgaard; Stephen V. Faraone; Thomas Werge; Jonas Bybjerg-Grauholm; Anders D. Børglum; Esben Agerbo; Honghui Yao; Zheng Chang; Isabell Brikell; Ditte Demontis
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Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling122,341例欧洲血统病例中主要焦虑疾病的全基因组关联研究确定了58个基因座并突出了gaba能信号传导
err2026-02-03
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errOAAI
errNora I. Strom; Brad Verhulst; Silviu-Alin Bacanu; Rosa Cheesman; Kirstin L. Purves; Hüseyin Gedik; Brittany L. Mitchell; Alex S. Kwong; Annika B. Faucon; Kritika Singh; Sarah Medland; Lucia Colodro-Conde; Kristi Krebs; Per Hoffmann; Stefan Herms; Jan Gehlen; Stephan Ripke; Swapnil Awasthi; Teemu Palviainen; Elisa M. Tasanko; Roseann E. Peterson; Daniel E. Adkins; Andrey A. Shabalin; Mark J. Adams; Matthew H. Iveson; Archie Campbell; Laurent F. Thomas; Bendik S. Winsvold; Ole Kristian Drange; Sigrid Børte; Abigail R. ter Kuile; Joonas Naamanka; Tan-Hoang Nguyen; Sandra M. Meier; Elizabeth C. Corfield; Laurie Hannigan; Daniel F. Levey; Darina Czamara; Heike Weber; Karmel W. Choi; Giorgio Pistis; Baptiste Couvy-Duchesne; Sandra Van der Auwera; Alexander Teumer; Robert Karlsson; Miguel Garcia-Argibay; Donghyung Lee; Rujia Wang; Ottar Bjerkeset; Eystein Stordal; Julia Bäckman; Giovanni A. Salum; Clement C. Zai; James L. Kennedy; Gwyneth Zai; Arun K. Tiwari; Stefanie Heilmann-Heimbach; Börge Schmidt; Jaakko Kaprio; Martin M. Kennedy; Joseph Boden; Alexandra Havdahl; Christel M. Middeldorp; Fabiana L. Lopes; Nirmala Akula; Francis J. McMahon; Elisabeth B. Binder; Lydia Fehm; Andreas Ströhle; Enrique Castelao; Henning Tiemeier; Dan J. Stein; David Whiteman; Catherine Olsen; Zachary Fuller; Xin Wang; Naomi R. Wray; Enda M. Byrne; Glyn Lewis; Nicholas J. Timpson; Lea K. Davis; Ian B. Hickie; Nathan A. Gillespie; Lili Milani; Johannes Schumacher; David P. Woldbye; Andreas J. Forstner; Markus M. Nöthen; Iiris Hovatta; John Horwood; William E. Copeland; Hermine H. Maes; Andrew M. McIntosh; Ole A. Andreassen; John-Anker Zwart; Ole Mors; Anders D. Børglum; Preben B. Mortensen; Helga Ask; Ted Reichborn-Kjennerud; Jackob M. Najman; Murray B. Stein; Joel Gelernter; Yuri Milaneschi; Brenda W. Penninx; Dorret I. Boomsma; Eduard Maron; Angelika Erhardt-Lehmann; Christian Rück; Tilo T. Kircher; Christiane A. Melzig; Georg W. Alpers; Volker Arolt; Katharina Domschke; Jordan W. Smoller; Martin Preisig; Nicholas G. Martin; Michelle K. Lupton; Annemarie I. Luik; Andreas Reif; Hans J. Grabe; Henrik Larsson; Patrik K. Magnusson; Albertine J. Oldehinkel; Catharina A. Hartman; Gerome Breen; Anna R. Docherty; Hilary Coon; Rupert Conrad; Kelli Lehto; Jürgen Deckert; Thalia C. Eley; Manuel Mattheisen; John M. Hettema
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Mapping the genetic landscape across 14 psychiatric disorders绘制14种精神疾病的遗传图谱
errNature
IF48.5
err2025-12-10
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errOAAI
errAndrew D. Grotzinger; Josefin Werme; Wouter J. Peyrot; Oleksandr Frei; Christiaan de Leeuw; Lucy K. Bicks; Qiuyu Guo; Michael P. Margolis; Brandon J. Coombes; Anthony Batzler; Vanessa Pazdernik; Joanna M. Biernacka; Ole A. Andreassen; Verneri Anttila; Anders D. Børglum; Gerome Breen; Na Cai; Ditte Demontis; Howard J. Edenberg; Stephen V. Faraone; Barbara Franke; Michael J. Gandal; Joel Gelernter; Alexander S. Hatoum; John M. Hettema; Emma C. Johnson; Katherine G. Jonas; James A. Knowles; Karestan C. Koenen; Adam X. Maihofer; Travis T. Mallard; Manuel Mattheisen; Karen S. Mitchell; Benjamin M. Neale; Caroline M. Nievergelt; John I. Nurnberger; Kevin S. O’Connell; Roseann E. Peterson; Elise B. Robinson; Sandra S. Sanchez-Roige; Susan L. Santangelo; Jeremiah M. Scharf; Hreinn Stefansson; Kari Stefansson; Murray B. Stein; Nora I. Strom; Laura M. Thornton; Elliot M. Tucker-Drob; Brad Verhulst; Irwin D. Waldman; G. Bragi Walters; Naomi R. Wray; Dongmei Yu; Phil H. Lee; Kenneth S. Kendler; Jordan W. Smoller
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Rare genetic variants confer a high risk of ADHD and implicate neuronal biology稀有遗传变异会增加ADHD的风险,并涉及神经元生物学。
errNature
IF48.5
err2025-11-12
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errOAAI
errDitte Demontis; Jinjie Duan; Yu-Han H. Hsu; Greta Pintacuda; Jakob Grove; Trine Tollerup Nielsen; Janne Thirstrup; Makayla Martorana; Travis Botts; F. Kyle Satterstrom; Jonas Bybjerg-Grauholm; Jason H. Y. Tsai; Simon Glerup; Martine Hoogman; Jan Buitelaar; Marieke Klein; Georg C. Ziegler; Christian Jacob; Oliver Grimm; Maximilian Bayas; Nene F. Kobayashi; Sarah Kittel-Schneider; Klaus-Peter Lesch; Barbara Franke; Andreas Reif; Esben Agerbo; Thomas Werge; Merete Nordentoft; Ole Mors; Preben Bo Mortensen; Kasper Lage; Mark J. Daly; Benjamin M. Neale; Anders D. Børglum
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Polygenic and developmental profiles of autism differ by age at diagnosis自闭症的多基因和发育特征因诊断年龄而异
errNature
IF48.5
err2025-10-01
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errOAAI
errXinhe Zhang; Jakob Grove; Yuanjun Gu; Cornelia K. Buus; Lea K. Nielsen; Sharon A. S. Neufeld; Mahmoud Koko; Daniel S. Malawsky; Emma M. Wade; Ellen Verhoef; Anna Gui; Laura Hegemann; Daniel H. Geschwind; Naomi R. Wray; Alexandra Havdahl; Angelica Ronald; Beate St Pourcain; Elise B. Robinson; Thomas Bourgeron; Simon Baron-Cohen; Anders D. Børglum; Hilary C. Martin; Varun Warrier
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A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activity在一个ADHD家庭中鉴定出的低频有害SORCS2变异体破坏了受体稳定性并抑制了其活性。
err2025-09-18
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errOAAI
errMathias Kaas; Sarah Broholt Dinesen; Ole Ahlgreen; Peder Madsen; Simon Mølgaard; Anders Dalby; Camilla Gustafsen; Ditte Olsen; Jinjie Duan; Joachim Vilstrup; Jonas Lende; Sanne Nordestgaard; Tetyana Zayats; Per Morten Knappskog; Stefan Johansson; Gesche Neckelmann; Barbara Franke; Søren Thirup; Anders Børglum; Andreas Reif; Christian Vægter; Ditte Demontis; Jan Haavik; Simon Glerup; Sune Skeldal
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Multi-site, multi-ancestry, genome-wide association study meta-analysis of functional seizure disorder in a hospital sample of 675,680 patients多中心、多祖先背景的医院样本功能性癫痫障碍全基因组关联研究荟萃分析(样本量为675,680例患者)
err2025-09-02
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errOAAI
errSlavina B. Goleva; Costin Leu; Yen-Chen Anne Feng; David Burstein; Sanan Venkatesh; Rebecca Birnbaum; Veera M. Rajagopal; Peter Straub; Jakob Christensen; Jocelyn F. Bautista; Robyn M. Busch; Imad M. Najm; Jakob Grove; Anders D. Børglum; Georgios Voloudakis; Panos Roussos; Jordan Smoller; Dennis Lal; Lea K. Davis
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Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses遗传结构及5种精神科诊断下的童年虐待风险
err2025-05-09
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PREAI
errNielsen, Trine Tollerup; Bali, Paraskevi; Grove, Jakob; Mohr-Jensen, Christina; Werge, Thomas; Dalsgaard, Soren; Borglum, Anders D.; Sonuga-Barke, Edmund; Minnis, Helen; Demontis, Ditte
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Polygenic scores for autism are associated with reduced neurite density in adults and children from the general population自闭症的多基因评分与普通人群中成人和儿童的树突密度降低相关
err2025-02-24
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errOAAI
errGu, Yuanjun; Maria-Stauffer, Eva; Bedford, Saashi A.; Adhya, Deep; Allison, Carrie; Ayeung, Bonnie; Bamford, Rosie; Bethlehem, Richard; Biron-Shental, Tal; Burton, Graham; Davies, Jonathan; Davis, Joanna; Floris, Dori; Franklin, Alice; Gabis, Lidia; Geschwind, Daniel; Greenberg, David M.; Havdahl, Alexandra; Heazell, Alexander; Holt, Rosemary; Hurles, Matthew; Khan, Yumnah; Lai, Meng-Chuan; Lancaster, Madeline; Lombardo, Michael; Martinez, Jose Gonzalez; Mill, Jonathan; Musa, Mahmoud Koko; Niakan, Kathy; Pavlinek, Adam; Polit, Lucia Dutan; Radecki, Marcin; Rowitch, David; Sichlinger, Laura; Srivastava, Deepak; Tsompanidis, Alexandros; Uzefovsky, Florina; Weir, Elizabeth; Zhang, Xinhe; Borglum, Anders; Bybjerg-Grauholm, Jonas; Hougaard, David M.; Mors, Ole; Mortensen, Preben Bo; Nordentoft, Merete; Werge, Thomas; Romero-Garcia, Rafael; Grove, Jakob; Borglum, Anders D.; Martin, Hilary; Baron-Cohen, Simon; Bethlehem, Richard A. I.; Warrier, Varun
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High level of immunoglobulin G targeting mycoplasma or cytomegalovirus in the newborn increases risk of ADHD高水平的免疫球蛋白G靶向支原体或巨细胞病毒在新生儿增加ADHD的风险
err2025-01-01
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errOAAI
errBorbye-Lorenzen, Nis; Holmgaard, Solveig; Ottosson, Filip; Nudel, Ron; Appadurai, Vivek; Laursen, Thomas Munk; Baekvad-Hansen, Marie; Bybjerg-Grauholm, Jonas; Nordentoft, Merete; Borglum, Anders D.; Mortensen, Preben Bo; Werge, Thomas; Benros, Michael E.; Hougaard, David Michael; Skogstrand, Kristin
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Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort
err2025-01-01
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errOAAI
errAkter, Hosneara; Rahaman, Md. Atikur; Eshaque, Tamannyat Binte; Mohamed, Nesrin; Islam, Amirul; Morshed, Mehzabin; Shahin, Zaha; Muhaimin, Al; Foyzullah, Arif Md.; Mim, Rabeya Akter; Omar, Farjana Binta; Hasan, Md. Nahid; Satsangi, Dharana; Ahmed, Nahid; Al Saba, Abdullah; Jahan, Nargis; Hossen, Md. Arif; Mondol, Md. Ashadujjaman; Sakib, Ahammad Sharif; Kabir, Rezwana; Chowdhury, Mohammod Shah Jahan; Shams, Nusrat; Afroz, Shireen; Kanta, Shayla Imam; Bhuiyan, Sarwar Jahan; Biswas, Rabi; Hanif, Shehzad; Tambi, Richa; Nassir, Nasna; Rahman, Muhammad Mizanur; Duan, Jinjie; Borglum, Anders D.; Amin, Robed; Basiruzzaman, Mohammed; Kamruzzaman, Md.; Sarker, Shaoli; Woodbury-Smith, Marc; Uddin, K. M. Furkan; Nabi, A. H. M. Nurun; Uddin, Mohammed
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Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study
err2024-12-01
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PREAI
errBreinbjerg, Anders; Jorgensen, Cecilie Siggaard; Walters, G. Bragi; Grove, Jakob; Als, Thomas D.; Kamperis, Konstantinos; Stefansdottir, Lilja; Thirstrup, Janne P.; Borg, Britt; Albinana, Clara; Vilhjalmsson, Bjarni J.; Eovarosson, Vioar O.; Stefansson, Hreinn; Mortensen, Preben B.; Agerbo, Esben; Werge, Thomas; Borglum, Anders; Demontis, Ditte; Stefansson, Kari; Rittig, Soren; Christensen, Jane Hvarregaard
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Sex differences in shared genetic determinants between severe mental disorders and metabolic traits
err2024-12-01
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errOAAI
errPisanu, Claudia; Congiu, Donatella; Meloni, Anna; Paribello, Pasquale; Severino, Giovanni; Ardau, Raffaella; Chillotti, Caterina; Als, Thomas D.; Borglum, Anders D.; Del Zompo, Maria; Manchia, Mirko; Squassina, Alessio
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The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder共同发生的条件和遗传学在进食障碍与注意力缺陷/多动障碍和自闭症谱系障碍的关联中的作用
err2024-11-14
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errOAAI
errChristiansen, Gitte Bundgaard; Petersen, Liselotte Vogdrup; Chatwin, Hannah; Yilmaz, Zeynep; Schendel, Diana; Bulik, Cynthia M.; Grove, Jakob; Brikell, Isabell; Semark, Birgitte Dige; Holde, Katrine; Abdulkadir, Mohamed; Hubel, Christopher; Albinana, Clara; Vilhjalmsson, Bjarni Johann; Borglum, Anders D.; Demontis, Ditte; Mortensen, Preben Bo; Larsen, Janne Tidselbak
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Polygenic liabilities and treatment trajectories in early-onset depression: a Danish register-based study早发性抑郁症的多基因责任和治疗轨迹: 一项基于丹麦注册的研究
err2024-10-14
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errOAAI
errMundy, Jessica; Hall, Alisha S. M.; Steinbach, Jette; Albinana, Clara; Agerbo, Esben; Als, Thomas D.; Thapar, Anita; McGrath, John J.; Vilhjalmsson, Bjarni J.; Nordentoft, Merete; Werge, Thomas; Borglum, Anders; Mortensen, Preben B.; Musliner, Katherine L.
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BEYOND DIAGNOSTICS: A DIMENSIONAL APPROACH TO MENTAL HEALTH PROFILING
err2024-10-01
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PREAI
errQvist, Per; Morch, Niels; Calderon, Andres Barrena; Kvamme, Timo; Donskov, Julie; Durand, Simon; Ottoson, Filip; Ernst, Madeleine; Sandberg, Kristian; Borglum, Anders
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UNRAVELING THE EVOLUTIONARY NATURE OF AUTISM SPECTRUM DISORDER FROM A GENOMIC PERSPECTIVE
err2024-10-01
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PREAI
errBada-Navarro, Ariadna; Casanova, Carla; Aranda, Selena; Koller, Dora; Ganau, Francesc; Demontis, Ditte; Borglum, Anders; Lao, Oscar; Mitjans, Marina; Cormand, Bru
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