Bibliografia UJ CM

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Amand F. Schmidt, Michael V. Holmes, David Preiss, Daniel I. Swerdlow, Spiros Denaxas, Ghazaleh Fatemifar, Rupert Faraway, Chris Finan, Dennis Valentine, Zammy Fairhurst-Hunter, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hypponen, Christine Power, Max Moldovan, Erik van Iperen, Kees Hovingh, Ilja Demuth, Kristina Norman, Elisabeth Steinhagen-Thiessen, Juri Demuth, Lars Bertram, Christina M. Lill, Stefan Coassin, Johann Willeit, Stefan Kiechl, Karin Willeit, Dan Mason, John Wright, Richard Morris, Goya Wanamethee, Peter Whincup, Yoav Ben-Shlomo, Stela McLachlan, Jackie F. Price, Mika Kivimaki, Catherine Welch, Adelaida Sanchez-Galvez, Pedro Marques-Vidal, Andrew Nicolaides, Andrie G. Panayiotou, N. Charlotte Onland-Moret, Yvonne T. van der Schouw, Giuseppe Matullo, Giovanni Fiorito, Simonetta Guarrera, Carlotta Sacerdote, Nicholas J. Wareham, Claudia Langenberg, Robert A. Scott, Jian'an Luan, Martin Bobak, Sofia Malyutina, Andrzej Pająk, Ruzena Kubinova, Abdonas Tamosiunas, Hynek Pikhart, Niels Grarup, Oluf Pedersen, Torben Hansen, Allan Linneberg, Tine Jess, Jackie Cooper, Steve E. Humphries, Murray Brilliant, Terrie Kitchner, Hakon Hakonarson, David S. Carrell, Catherine A. McCarty, Kirchner H. Lester, Eric B. Larson, David R. Crosslin, Mariza de Andrade, Dan M. Roden, Joshua C. Denny, Cara Carty, Stephen Hancock, John Attia, Elizabeth Holliday, Rodney Scott, Peter Schofield, Martin O'Donnell, Salim Yusuf6, Michael Chong, Guillaume Pare, Pim van der Harst, M. Abdullah Said, Ruben N. Eppinga, Niek Verweij, Harold Snieder, Tim Christen, D. O. Mook-Kanamori, Lars Lind, Erik Ingelsson, Raha Pazoki, Oscar Franco, Albert Hofman, Andre Uitterlinden, Abbas Dehghan, Alexander Teumer, Sebastian Baumeister, Marcus Dorr, Markus M. Lerch, Uwe Volker, Henry Volzke, Joey Ward, Jill P. Pell, Tom Meade, Ingrid E. Christophersen, Anke H. Maitland-van der Zee, Ekaterina V. Baranova, Robin Young, Ian Ford, Archie Campbell, Sandosh Padmanabhan, Michiel L. Bots, Diederick E. Grobbee, Philippe Froguel, Dorothee Thuillier, Ronan Roussel, Amelie Bonnefond, Bertrand Cariou, Melissa Smart, Yanchun Bao, Meena Kumari, Anubha Mahajan, Jemma C. Hopewell, Sudha Seshadri, Caroline Dale, Rui Providencia E. Costa, Paul M. Ridker, Daniel I. Chasman, Alex P. Reiner, Marylyn D. Ritchie, Leslie A. Lange, Alex J. Cornish, Sara E. Dobbins, Kari Hemminki, Ben Kinnersley, Marc Sanson, Karim Labreche, Matthias Simon, Melissa Bondy, Philip Law, Helen Speedy, James Allan, Ni Li, Molly Went, Niels Weinhold, Gareth Morgan, Pieter Sonneveld, Bjorn Nilsson, Hartmut Goldschmidt, Amit Sud, Andreas Engert, Markus Hansson, Harry Hemingway, Folkert W. Asselbergs, Riyaz S. Patel, Brendan J. Keating, Naveed Sattar, Richard Houlston, Juan P. Casas, Aroon D. Hingorani.
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9.
BMC Cardiovascular Disorders
2019 : Vol. 19, il., bibliogr. 38 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 4.0.
Autor korespondencyjny: Amand F. Schmidt.
p-ISSN: 1471-2261
AZ
ORG
AIF
IF: 2.078
Adres url:
Streszczenie w PubMed:
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Amand F. Schmidt, Daniel I. Swerdlow, Michael V. Holmes, Riyaz S. Patel, Zammy Fairhurst-Hunter, Donald M. Lyall, Fernando Pires Hartwig, Bernardo Lessa Horta, Elina Hypponen, Christine Power, Max Moldovan, Erik van Iperen, G. Kees Hovingh, Ilja Demuth, Kristina Norman, Elisabeth Steinhagen-Thiessen, Juri Demuth, Lars Bertram, Tian Liu, Stefan Coassin, Johann Willeit, Stefan Kiechl, Karin Willeit, Dan Mason, John Wright, Richard Morris, Goya Wanamethee, Peter Whincup, Yoav Ben-Shlomo, Stela McLachlan, Jackie F. Price, Mika Kivimaki, Catherine Welch, Adelaida Sanchez-Galvez, Pedro Marques-Vidal, Andrew Nicolaides, Andrie G. Panayiotou, N. Charlotte Onland-Moret, Yvonne T. van der Schouw, Giuseppe Matullo, Giovanni Fiorito, Simonetta Guarrera, Carlotta Sacerdote, Nicholas J. Wareham, Claudia Langenberg, Robert Scott, Jian'an Luan, Martin Bobak, Sofia Malyutina, Andrzej Pająk, Ruzena Kubinova, Abdonas Tamosiunas, Hynek Pikhart, Lise Lotte Nystrup Husemoen, Niels Grarup, Oluf Pedersen, Torben Hansen, Allan Linneberg, Kenneth Starup Simonsen, Jackie Cooper, Steve E. Humphries, Murray Brilliant, Terrie Kitchner, Hakon Hakonarson, David S. Carrell, Catherine A. McCarty, H. Lester Kirchner, Eric B. Larson, David R. Crosslin, Mariz de Andrade, Dan M. Roden, Joshua C. Denny, Cara Carty, Stephen Hancock, John Attia, Elizabeth Holliday, Martin O' Donnell, Salim Yusuf, Michael Chong, Guillaume Pare, Pim van der Harst, M. Abdullah Said, Ruben N. Eppinga, Niek Verweij, Harold Snieder, Tim Christen, Dennis O. Mook-Kanamori, Stefan Gustafsson, Lars Lind, Erik Ingelsson, Raha Pazoki, Oscar Franco, Albert Hofman, Andre Uitterlinden, Abbas Dehghan, Alexander Teumer, Sebastian Baumeister, Marcus Dorr, Markus M. Lerch, Uwe Volker, Henry Volzke, Joey Ward, Jill P. Pell, Daniel J. Smith, Tom Meade, Anke H. Maitland-van der Zee, Ekaterina V. Baranova, Robin Young, Ian Ford, Archie Campbell, Sandosh Padmanabhan, Michiel L. Bots, Diederick E. Grobbee, Philippe Froguel, Dorothee Thuillier, Beverley Balkau, Amélie Bonnefond, Bertrand Cariou, Melissa Smart, Yanchun Bao, Meena Kumari, Anubha Mahajan, Paul M. Ridker, Daniel I. Chasman, Alex P. Reiner, Leslie A. Lange, Marylyn D. Ritchie, Folkert W. Asselbergs, Juan-Pablo Casas, Brendan J. Keating, David Preiss, Aroon D. Hingorani, Naveed Sattar.
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.
Lancet. Diabetes & Endocrinology
2017 : Vol. 5, nr 2, s. 97-105, il., bibliogr. 41 poz., summ.
Autor korespondencyjny: Amand F. Schmidt.
p-ISSN: 2213-8587
AZ
ORG
AIF
IF: 19.313
Adres url:
Streszczenie w PubMed:
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Gaya Thanabalasingham, Neha Shah, Martine Vaxillaire, Torben Hansen, Juraj Stanik, Magdalena Szopa, Erling Tjora, Timothy J. James, Paula Kokko, Francois Loiseleur, Mark I. McCarthy, Philippe Froguel, Oluf B. Pedersen, Leif Groop, Daniela Gasperikova, Maciej T. Malecki, Pal R. Njolstad, Anna L. Gloyn, Katharine R. Owen.
A large multi-centre european validation study confirms that highly sensitive c-reactive protein (hsCRP) is a clinically useful biomarker for maturity onset diabetes of the young (MODY) due to HNF1A mutations.
Diabetes
2011 : Vol. 60, suppl. 1, s. A389, abstr. 1412-P
71st Scientific Sessions, San Diego, CA, June 24-June 28, 2011
p-ISSN: 0012-1797
SZZ
SIF
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Takafumi Tsuchiya, Peter E.H. Schwarz, Laura Bosque-Plata, del, M. Geoffrey Hayes, Christian Dina, Philippe Froguel, G. Wayne Towers, Sabine Fischer, Theodora Temelkova-Kurktschiev, Hannes Rietzsch, Juergen Graessler, Josef Vcelák, Daniela Palyzová, Thomas Selisko, Bela Bendlová, Jan Schulze, Ulrich Julius, Markolf Hanefeld, Michael N. Weedon, Julie C. Evans, Timothy M. Frayling, Andrew T. Hattersley, Marju Orho-Melander, Leif Groop, Maciej T. Malecki, Torben Hansen, Oluf Pedersen, Tasha E. Fingerlin, Michael Boehnke, Craig L. Hanis, Nancy J. Cox, Graeme I. Bell.
Association of the calpain-10 gene with type 2 diabetes in Europeans : results of pooled and meta-analyses.
Molecular Genetics and Metabolism
2006 : Vol. 89, nr 1-2, s. 174-184, bibliogr., abstr.
AZ
ORG
AIF
IF: 2.371
Adres url:
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