Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Simone M. Cross"'
Autor:
Rosalie B. T. M. Sterenborg, Inga Steinbrenner, Yong Li, Melissa N. Bujnis, Tatsuhiko Naito, Eirini Marouli, Tessel E. Galesloot, Oladapo Babajide, Laura Andreasen, Arne Astrup, Bjørn Olav Åsvold, Stefania Bandinelli, Marian Beekman, John P. Beilby, Jette Bork-Jensen, Thibaud Boutin, Jennifer A. Brody, Suzanne J. Brown, Ben Brumpton, Purdey J. Campbell, Anne R. Cappola, Graziano Ceresini, Layal Chaker, Daniel I. Chasman, Maria Pina Concas, Rodrigo Coutinho de Almeida, Simone M. Cross, Francesco Cucca, Ian J. Deary, Alisa Devedzic Kjaergaard, Justin B. Echouffo Tcheugui, Christina Ellervik, Johan G. Eriksson, Luigi Ferrucci, Jan Freudenberg, GHS DiscovEHR, Regeneron Genetics Center, Christian Fuchsberger, Christian Gieger, Franco Giulianini, Martin Gögele, Sarah E. Graham, Niels Grarup, Ivana Gunjača, Torben Hansen, Barbara N. Harding, Sarah E. Harris, Stig Haunsø, Caroline Hayward, Jennie Hui, Till Ittermann, J. Wouter Jukema, Eero Kajantie, Jørgen K. Kanters, Line L. Kårhus, Lambertus A. L. M. Kiemeney, Margreet Kloppenburg, Brigitte Kühnel, Jari Lahti, Claudia Langenberg, Bruno Lapauw, Graham Leese, Shuo Li, David C. M. Liewald, Allan Linneberg, Jesus V. T. Lominchar, Jian’an Luan, Nicholas G. Martin, Antonela Matana, Marcel E. Meima, Thomas Meitinger, Ingrid Meulenbelt, Braxton D. Mitchell, Line T. Møllehave, Samia Mora, Silvia Naitza, Matthias Nauck, Romana T. Netea-Maier, Raymond Noordam, Casia Nursyifa, Yukinori Okada, Stefano Onano, Areti Papadopoulou, Colin N. A. Palmer, Cristian Pattaro, Oluf Pedersen, Annette Peters, Maik Pietzner, Ozren Polašek, Peter P. Pramstaller, Bruce M. Psaty, Ante Punda, Debashree Ray, Paul Redmond, J. Brent Richards, Paul M. Ridker, Tom C. Russ, Kathleen A. Ryan, Morten Salling Olesen, Ulla T. Schultheiss, Elizabeth Selvin, Moneeza K. Siddiqui, Carlo Sidore, P. Eline Slagboom, Thorkild I. A. Sørensen, Enrique Soto-Pedre, Tim D. Spector, Beatrice Spedicati, Sundararajan Srinivasan, John M. Starr, David J. Stott, Toshiko Tanaka, Vesela Torlak, Stella Trompet, Johanna Tuhkanen, André G. Uitterlinden, Erik B. van den Akker, Tibbert van den Eynde, Melanie M. van der Klauw, Diana van Heemst, Charlotte Verroken, W. Edward Visser, Dina Vojinovic, Henry Völzke, Melanie Waldenberger, John P. Walsh, Nicholas J. Wareham, Stefan Weiss, Cristen J. Willer, Scott G. Wilson, Bruce H. R. Wolffenbuttel, Hanneke J. C. M. Wouters, Margaret J. Wright, Qiong Yang, Tatijana Zemunik, Wei Zhou, Gu Zhu, Sebastian Zöllner, Johannes W. A. Smit, Robin P. Peeters, Anna Köttgen, Alexander Teumer, Marco Medici
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract To date only a fraction of the genetic footprint of thyroid function has been clarified. We report a genome-wide association study meta-analysis of thyroid function in up to 271,040 individuals of European ancestry, including reference range
Externí odkaz:
https://doaj.org/article/87582eb11e3e4880b14ffaaf73048c8f
Autor:
Phillip E. Melton, Scott Wilson, Carol A. Wang, Trevor A. Mori, Gu Zhu, Frank Dudbridge, Suzanne J. Brown, Sarah E. Medland, Scott D. Gordon, Ee Mun Lim, Nicholas G. Martin, Purdey J Campbell, Craig E. Pennell, John Joseph, John P. Walsh, Lawrence J. Beilin, James Nolan, Simone M. Cross, Benjamin H. Mullin, Vijay Panicker
Publikováno v:
European journal of endocrinology. 185(5)
Objective Genetic factors underpin the narrow intraindividual variability of thyroid function, although precise contributions of environmental vs genetic factors remain uncertain. We sought to clarify the heritability of thyroid function traits and t
Autor:
Danuta Z. Loesch, Miguel E. Rentería, Clemens R. Scherzer, Gratten J, Aoibhe Mulcahy, Philip E. Mosley, Poortvliet Pc, N. G. Martin, Adrian I. Campos, Luis M. García-Marín, George D. Mellick, Brittany L. Mitchell, Penelope A. Lind, Ferguson M, Bivol S, Simone M. Cross, Richard Parker, Peter M. Visscher, Sarah E. Medland
PurposeParkinson’s disease (PD) is a neurodegenerative disorder associated with progressive disability. While the precise aetiology is unknown, there is evidence of significant genetic and environmental influences on individual risk. The Australian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0a27c29f63b939103bf72ec7e30b0d
https://doi.org/10.1101/2021.04.02.21254825
https://doi.org/10.1101/2021.04.02.21254825
Autor:
Lenore Sullivan, Simone M. Cross, Katherine M. Kirk, Nicholas G. Martin, Ian B. Hickie, Enda M. Byrne, Dixie J. Statham, Naomi R. Wray, Julio Licinio, Richard Parker, John J. McGrath, Sarah E. Medland, Douglas F. Levinson
ObjectivesDepression is the most common psychiatric disorder and the largest contributor to global disability. The Australian Genetics of Depression study was established to recruit a large cohort of individuals who have been diagnosed with depressio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d695640788dab3620c8fbdb806001b2
Autor:
Lavinia Paternoster, Simone M. Cross, Merete Lund Maegbaek, Trine Munk-Olsen, Jodie N. Painter, Penelope A. Lind, Annika Gunst, Ada Johansson, Margaret J. Wright, Sarah E. Medland, Juan F. Sánchez-Romera, Juan R. Ordoñana, Dale R. Nyholt, Lucía Colodro-Conde, Patrick Jern
Publikováno v:
Colodro-Conde, L, Cross, S M, Lind, P A, Painter, J N, Gunst, A, Jern, P, Johansson, A, Lund Maegbaek, M, Munk-Olsen, T, Nyholt, D R, Ordoñana, J R, Paternoster, L, Sánchez-Romera, J F, Wright, M J & Medland, S E 2017, ' Cohort Profile : Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium) ', International Journal of Epidemiology, vol. 46, no. 2 . https://doi.org/10.1093/ije/dyv360
ResearcherID
International Journal of Epidemiology
Colodro-Conde, L, Cross, S M, Lind, P A, Painter, J N, Gunst, A, Jern, P, Johansson, A, Maegbaek, M L, Munk-Olsen, T, Nyholt, D R, Ordoñana, J R, Paternoster, L, Sánchez-Romera, J F, Wright, M J & Medland, S E 2017, ' Cohort Profile : Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium) ', International Journal of Epidemiology, vol. 46, no. 2, e17 . https://doi.org/10.1093/ije/dyv360
ResearcherID
International Journal of Epidemiology
Colodro-Conde, L, Cross, S M, Lind, P A, Painter, J N, Gunst, A, Jern, P, Johansson, A, Maegbaek, M L, Munk-Olsen, T, Nyholt, D R, Ordoñana, J R, Paternoster, L, Sánchez-Romera, J F, Wright, M J & Medland, S E 2017, ' Cohort Profile : Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium) ', International Journal of Epidemiology, vol. 46, no. 2, e17 . https://doi.org/10.1093/ije/dyv360
Nausea and vomiting during pregnancy (NVP), commonly known as morning sickness, is very common and is typically self-limiting. However, more severe forms and the development of hyperemesis gravidarum (HG), defined as persistent and excessive vomiting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3202868c72e72c8dc11718e7350136a1
https://pure.au.dk/ws/files/136135028/Cohort_profile_nausea_and_vomiting_during_pregnancy_VOR17.pdf
https://pure.au.dk/ws/files/136135028/Cohort_profile_nausea_and_vomiting_during_pregnancy_VOR17.pdf
Publikováno v:
Intervirology. 43:55-60
Cytokines and chemokines play important roles in both autoimmune and infectious arthritides. Here we describe the cytokines and chemokines induced by Ross River (RR) virus infection of synovial fibroblasts and macrophages in vitro. RR virus is the ae
Autor:
Naomi Kondo, Hideo Kaneko, Toshiyuki Fukao, Martin F. Lavin, I. S. Misko, Dianne Watters, Padmini Kedar, Toko Yoshida, H Tashita, Simone M. Cross, Kum Kum Khana, Geoff W. Birrell, Magtouf Gatei
Publikováno v:
Blood. 94:1998-2006
Patients with the human genetic disorder ataxia-telangiectasia (A-T) are characterized by immunodeficiency and a predisposition to develop lymphoid malignancies. The gene mutated in A-T patients, ATM, codes for a high molecular weight protein that is
Publikováno v:
International Journal of Cancer. 77:755-762
Burkitt's lymphoma cells that vary in their phenotypic characteristics show significantly different degrees of susceptibility to radiation-induced apoptosis. Propensity to undergo apoptosis is reflected in the degradation of substrates such as DNA-de
Autor:
Simone M. Cross, Sharon L. Silins, I. S. Misko, Suzanne L. Elliott, Denis J. Moss, Stephanie J. Pye, Jacqueline M. Burrows
Publikováno v:
International Immunology. 9:1745-1755
We investigated the CD8+ cytotoxic T lymphocyte (CTL) repertoire to an HLA B8-restricted peptide, RAKFKQLLQ, located in the Epstein-Barr virus (EBV) immediate-early protein, BZLF1. Repertoire selection was monitored by determining the TCR beta chain
Autor:
Suzanne L. Elliott, Sharon L. Silins, Jacqueline M. Burrows, Maureen Rischmueller, Scott R. Burrows, Simone M. Cross, Chen Au Peh, James McCluskey
Publikováno v:
European Journal of Immunology. 27:178-182
The memory response to the immunodominant Epstein-Barr virus (EBV) epitope FLRGRAYGL, which associates with HLA B8, is exceptionally restricted, being dominated by cytotoxic T lymphocytes (CTL) with a single, public T cell receptor (TCR). CTL clones