% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Junker:272821,
      author       = {Junker, Johanna and Lange, Lara Mariah and Vollstedt,
                      Eva-Juliane and Roopnarain, Karisha and Doquenia, Maria
                      Leila M and Annuar, Azlina Ahmad and Avenali, Micol and
                      Bardien, Soraya and Bahr, Natascha and Ellis, Melina and
                      Galandra, Caterina and Gasser, Thomas and Heutink, Peter and
                      Illarionova, Anastasia and Kanana, Yuliia and Keller
                      Sarmiento, Ignacio J and Kumar, Kishore R and Lim, Shen-Yang
                      and Madoev, Harutyun and Mata, Ignacio F and Mencacci,
                      Niccolò E and Nalls, Mike A and Padmanabhan, Shalini and
                      Shambetova, Cholpon and Solle, J. C. and Tan, Ai-Huey and
                      Trinh, Joanne and Valente, Enza Maria and Singleton, Andrew
                      and Blauwendraat, Cornelis and Lohmann, Katja and Fang,
                      Zih-Hua and Klein, Christine},
      collaboration = {Program, Global Parkinson's Genetics},
      othercontributors = {Junker, Johanna and Lange, Lara Mariah and Vollstedt,
                          Eva-Juliane and Roopnarain, Karisha and Doquenia, Maria
                          Leila M and Annuar, Azlina Ahmad and Avenali, Micol and
                          Bardien, Soraya and Bahr, Natascha and Ellis, Melina and
                          Galandra, Caterina and Gasser, Thomas and Heutink, Peter and
                          Illarionova, Anastasia and Kanana, Yuliia and Keller,
                          Ignacio J and Kumar, Kishore R and Lim, Shen-Yang and
                          Madoev, Harutyun and Mata, Ignacio F and Mencacci, Niccolò
                          E and Nalls's, Mike A and Padmanabhan, Shalini and
                          Shambetova, Cholpon and Solle, J. and Tan, Ai-Huey and
                          Trinh, Joanne and Valente, Enza Maria and Singleton, Andrew
                          and Blauwendraat, Cornelis and Lohmann, Katja and Fang,
                          Zih-Hua and Klein, Christine},
      title        = {{T}eam {S}cience {A}pproaches to {U}nravel {M}onogenic
                      {P}arkinson's {D}isease on a {G}lobal {S}cale.},
      journal      = {Movement disorders},
      volume       = {39},
      number       = {10},
      issn         = {0885-3185},
      address      = {New York, NY},
      publisher    = {Wiley},
      reportid     = {DZNE-2024-01239},
      pages        = {1868 - 1873},
      year         = {2024},
      abstract     = {Until recently, about three-quarters of all monogenic
                      Parkinson's disease (PD) studies were performed in
                      European/White ancestry, thereby severely limiting our
                      insights into genotype-phenotype relationships at a global
                      scale.To identify the multi-ancestry spectrum of monogenic
                      PD.The first systematic approach to embrace monogenic PD
                      worldwide, The Michael J. Fox Foundation Global Monogenic PD
                      Project, contacted authors of publications reporting
                      individuals carrying pathogenic variants in known PD-causing
                      genes. In contrast, the Global Parkinson's Genetics
                      Program's Monogenic Network took a different approach by
                      targeting PD centers underrepresented or not yet represented
                      in the medical literature.In this article, we describe
                      combining both efforts in a merger project resulting in a
                      global monogenic PD cohort with the buildup of a sustainable
                      infrastructure to identify the multi-ancestry spectrum of
                      monogenic PD and enable studies of factors modifying
                      penetrance and expressivity of monogenic PD.This effort
                      demonstrates the value of future research based on team
                      science approaches to generate comprehensive and globally
                      relevant results. © 2024 The Author(s). Movement Disorders
                      published by Wiley Periodicals LLC on behalf of
                      International Parkinson and Movement Disorder Society.},
      keywords     = {Humans / Parkinson Disease: genetics / Parkinson Disease:
                      therapy / Genetic Predisposition to Disease / Genetic
                      Association Studies: methods / GP2 (Other) / MJFF GMPD
                      (Other) / Parkinson's disease (Other) / monogenic
                      Parkinson's disease (Other) / parkinsonism (Other)},
      cin          = {AG Gasser / AG Heutink / ICRU},
      ddc          = {610},
      cid          = {I:(DE-2719)1210000 / I:(DE-2719)1210002 /
                      I:(DE-2719)1240005},
      pnm          = {353 - Clinical and Health Care Research (POF4-353) / 354 -
                      Disease Prevention and Healthy Aging (POF4-354) / 899 - ohne
                      Topic (POF4-899)},
      pid          = {G:(DE-HGF)POF4-353 / G:(DE-HGF)POF4-354 /
                      G:(DE-HGF)POF4-899},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:39076159},
      doi          = {10.1002/mds.29925},
      url          = {https://pub.dzne.de/record/272821},
}