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Tytuł:
Association of Factor V Leiden With Subsequent Atherothrombotic Events : a GENIUS-CHD Study of Individual Participant Data
Autorzy:
Delgado, Graciela
Pilbrow, Anna
Wallentin, Lars
Lang, Chim
Nikus, Kjell
Patel, Riyaz
Simon, Tabassome
Gong, Yan
Pare, Guillaume
Deloukas, Panos
James, Stefan
Laurikka, Jari
Szczeklik, Wojciech
Holmes, Michael
Muehlschlegel, Jochen
Stewart, Alexandre
Hartiala, Jaana
Hovingh, G.
Dudbridge, Frank
Richards, A.
Baranova, Ekaterina
Scholz, Markus
Cresci, Sharon
Gijsberts, Crystel
McPherson, Ruth
Tang, W.H.
Danchin, Nicolas
Burkhardt, Ralph
McCubrey, Raymond
Mahmoodi, Bakhtawar
Pepine, Carl
Grobbee, Diederick
Kleber, Marcus
Direk, Kenan
ten Berg, Jurriën
Johnson, Julie
Levin, Daniel
Bots, Michiel
Kaczor, Marcin
Doughty, Robert
Schmidt, Amand
van Setten, Jessica
Sanak, Marek
Lenzini, Petra
Klungel, Olaf
Cooper-DeHoff, Rhonda
Body, Simon
Hingorani, Aroon
van der Laan, Sander
Tragante, Vinicius
Nelson, Christopher
Deanfield, John
Spertus, John
Held, Claes
Kähönen, Mika
Sattar, Naveed
Lehtimäki, Terho
Visseren, Frank
Teren, Andrej
Allayee, Hooman
Waltenberger, Johannes
Hoefer, Imo
Maitland-van der Zee, Anke
Akerblom, Axel
Kraaijeveld, Adriaan
Palmer, Colin
Kuukasjarvi, Pekka
Eriksson, Niclas
Mordi, Ify
Hazen, Stanley
Heydarpour, Mahyar
Pasterkamp, Gerard
März, Winfried
Hagström, Emil
Asselbergs, Folkert
Bergmeijer, Thomas
Cameron, Vicky
Lyytikäinen, Leo-Pekka
Thiery, Joachim
Braund, Peter
Samani, Nilesh
Vilmundarson, Ragnar
Howe, Laurence
Kotti, Salma
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Contribution of common genetic variants to risk of early-onset ischemic stroke
Autorzy:
Jimenez-Conde, Jordi
Ryan, Kathleen A.
Luke, Sothear
Gieger, Christian
Pera, Joanna
Thijs, Vincent
Smith, Jennifer A.
Mitchell, Braxton D.
Chong, Michael
Rexrode, Kathryn
Cruchaga, Carlos
Torres-Aguila, Nuria P.
Markus, Hugh S.
Heitsch, Laura
Walters, Robin G.
Li, Jiang
Rosand, Jonathan
Jaworek, Thomas
Kamatani, Yoichiro
Meschia, James F.
Holliday, Elizabeth
Mcardle, Patrick F.
Anderson, Christopher D.
Ilinca, Andreea
Bell, Steven
Cushman, Mary
Gaynor, Brady J.
Muller-Nurasyid, Martina
Putaala, Jukka
Cole, John W.
Engstrom, Gunnar
Grittner, Ulrike
Strbian, Daniel
Kardia, Sharon L.R.
Levi, Christopher R.
Hong, Charles C.
O'Donnell, Martin
Pare, Guillaume
Zand, Ramin
Tuladhar, Anil M.
Faul, Jessica D.
Havulinna, Aki S.
Sacco, Ralph L.
Mcdonough, Caitrin W.
Jern, Christina
Boncoraglio, Giorgio B.
Hu, Jie
Rothwell, Peter M.
Metso, Tiina
Lin, Kuang
Giese, Anne-Katrin
Fecteau, Natalie S.
Jackson, Rebecca D.
Johnson, Julie A.
Ribases, Marta
Attia, John
Veldink, Jan H.
de Leeuw, Frank-Erik
Lemmens, Robin
O'Connor, Timothy D.
Danesh, John
Irvin, Marguerite R.
Perry, James A.
Hochberg, Marc C.
Stine, O. Colin
Fernandez-Cadenas, Israel
Tomppo, Liisa
Abedi, Vida
Grewal, Raji P.
Li, Liming
Sanchez-Mora, Cristina
Lange, Leslie
Ross, Owen A.
Chen, Zhengming
Debette, Stephanie
Wassertheil-Smoller, Sylvia
Stanne, Tara M.
Jacob, Mina A.
Smith, Nicholas L.
Dichgans, Martin
Sudlow, Cathie L.M.
Kittner, Steven J.
Rannikmae, Kristiina
Peddareddygari, Leema R.
Lopez, Haley
Peters, Annette
Benavente, Oscar R.
Weir, David R.
Salomaa, Veikko
Enzinger, Chris
Lindgren, Arne G.
Tatlisumak, Turgut
Durda, Jon Peter
Ray, Debashree
Xu, Huichun
Lee, Jin-Moo
Worrall, Bradford B.
Butterworth, Adam
Słowik, Agnieszka
Soderholm, Martin
Woo, Daniel
Carcel-Marquez, Jara
Duggan, David J.
Maguire, Jane
Koido, Masaru
Sharma, Pankaj
Terao, Chikashi
Malik, Rainer
Schmidt, Reinhold
Amouyel, Philippe
Kubo, Michiaki
Rabionet, Raquel
Tregouet, David-Alexandre
Armstrong, Nicole D.
Rundek, Tatjana
Opis:
Background and Objectives:Current genome-wide association studies of ischemic stroke have focused primarily on late-onset disease. As a complement to these studies, we sought to identify the contribution of common genetic variants to risk of early-onset ischemic stroke: Methods: We performed a meta-analysis of genome-wide association studies of early-onset stroke (EOS), ages 18–59 years, using individual-level data or summary statistics in 16,730 cases and 599,237 nonstroke controls obtained across 48 different studies. We further compared effect sizes at associated loci between EOS and late-onset stroke (LOS) and compared polygenic risk scores (PRS) for venous thromboembolism (VTE) between EOS and LOS. Results: We observed genome-wide significant associations of EOS with 2 variants in ABO, a known stroke locus. These variants tag blood subgroups O1 and A1, and the effect sizes of both variants were significantly larger in EOS compared with LOS. The odds ratio (OR) for rs529565, tagging O1, was 0.88 (95% confidence interval [CI]: 0.85–0.91) in EOS vs 0.96 (95% CI: 0.92–1.00) in LOS, and the OR for rs635634, tagging A1, was 1.16 (1.11–1.21) for EOS vs 1.05 (0.99–1.11) in LOS; p-values for interaction = 0.001 and 0.005, respectively. Using PRSs, we observed that greater genetic risk for VTE, another prothrombotic condition, was more strongly associated with EOS compared with LOS (p = 0.008). Discussion: The ABO locus, genetically predicted blood group A, and higher genetic propensity for venous thrombosis are more strongly associated with EOS than with LOS, supporting a stronger role of prothrombotic factors in EOS.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
PCSK9 genetic variants and risk of type 2 diabetes : a mendelian randomisation study
Autorzy:
Bots, Michiel L.
Froguel, Philippe
Hypponen, Elina
Price, Jackie F.
Smart, Melissa
van Iperen, Erik
Hakonarson, Hakon
Lange, Leslie A.
Ridker, Paul M.
Moldovan, Max
Kiechl, Stefan
Kumari, Meena
Husemoen, Lise Lotte Nystrup
Liu, Tian
Patel, Riyaz S.
Mahajan, Anubha
Larson, Eric B.
Sanchez-Galvez, Adelaida
Ritchie, Marylyn D.
Pikhart, Hynek
Kitchner, Terrie
Willeit, Karin
Demuth, Juri
Verweij, Niek
Balkau, Beverley
Cariou, Bertrand
de Andrade, Mariz
Sacerdote, Carlotta
Morris, Richard
Matullo, Giuseppe
Young, Robin
Lerch, Markus M.
Kubinova, Ruzena
Christen, Tim
Malyutina, Sofia
Wareham, Nicholas J.
Chasman, Daniel I.
O' Donnell, Martin
Fairhurst-Hunter, Zammy
Uitterlinden, Andre
Scott, Robert
Hingorani, Aroon D.
Whincup, Peter
Power, Christine
Hancock, Stephen
Grarup, Niels
van der Schouw, Yvonne T.
Mason, Dan
Pająk, Andrzej
Tamosiunas, Abdonas
Guarrera, Simonetta
Mook-Kanamori, Dennis O.
Dorr, Marcus
Ward, Joey
Pare, Guillaume
Bobak, Martin
Pell, Jill P.
Hovingh, G. Kees
Bertram, Lars
Pedersen, Oluf
Kirchner, H. Lester
Gustafsson, Stefan
Linneberg, Allan
Carrell, David S.
Snieder, Harold
Baumeister, Sebastian
Hartwig, Fernando Pires
Ford, Ian
Casas, Juan-Pablo
Preiss, David
Ben-Shlomo, Yoav
Swerdlow, Daniel I.
Willeit, Johann
Fiorito, Giovanni
Holmes, Michael V.
Yusuf, Salim
Volker, Uwe
Denny, Joshua C.
Meade, Tom
Maitland-van der Zee, Anke H.
Panayiotou, Andrie G.
McLachlan, Stela
Lyall, Donald M.
Grobbee, Diederick E.
Coassin, Stefan
Wanamethee, Goya
Volzke, Henry
Kivimaki, Mika
Wright, John
Carty, Cara
Nicolaides, Andrew
Asselbergs, Folkert W.
Eppinga, Ruben N.
Langenberg, Claudia
Attia, John
Welch, Catherine
Padmanabhan, Sandosh
Brilliant, Murray
Marques-Vidal, Pedro
Bonnefond, Amélie
Franco, Oscar
Baranova, Ekaterina V.
Reiner, Alex P.
Teumer, Alexander
Keating, Brendan J.
Thuillier, Dorothee
Horta, Bernardo Lessa
Ingelsson, Erik
Humphries, Steve E.
Smith, Daniel J.
Lind, Lars
Hansen, Torben
Holliday, Elizabeth
van der Harst, Pim
Schmidt, Amand F.
Cooper, Jackie
Steinhagen-Thiessen, Elisabeth
Hofman, Albert
Dehghan, Abbas
Onland-Moret, N. Charlotte
Demuth, Ilja
Chong, Michael
Roden, Dan M.
Said, M. Abdullah
McCarty, Catherine A.
Crosslin, David R.
Campbell, Archie
Simonsen, Kenneth Starup
Luan, Jian'an
Bao, Yanchun
Sattar, Naveed
Pazoki, Raha
Norman, Kristina
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
Autorzy:
Denaxas, Spiros
Lester, Kirchner H.
Bondy, Melissa
Casas, Juan P.
Kitchner, Terrie
Fiorito, Giovanni
Roden, Dan M.
Hovingh, Kees
Swerdlow, Daniel I.
Hemminki, Kari
Nicolaides, Andrew
Mahajan, Anubha
Linneberg, Allan
Lill, Christina M.
Pazoki, Raha
Wright, John
Morris, Richard
Pare, Guillaume
Law, Philip
Price, Jackie F.
Welch, Catherine
Hakonarson, Hakon
Campbell, Archie
Panayiotou, Andrie G.
Eppinga, Ruben N.
Uitterlinden, Andre
Wareham, Nicholas J.
Cooper, Jackie
Malyutina, Sofia
Valentine, Dennis
Fairhurst-Hunter, Zammy
Christen, Tim
Ingelsson, Erik
Hopewell, Jemma C.
Lerch, Markus M.
Franco, Oscar
Costa, Rui Providencia E.
Sanchez-Galvez, Adelaida
Guarrera, Simonetta
Kiechl, Stefan
Asselbergs, Folkert W.
Hancock, Stephen
Speedy, Helen
Scott, Robert A.
Hansen, Torben
Goldschmidt, Hartmut
Meade, Tom
Froguel, Philippe
Brilliant, Murray
Lange, Leslie A.
Demuth, Ilja
McLachlan, Stela
Faraway, Rupert
Grobbee, Diederick E.
Bao, Yanchun
Engert, Andreas
Mason, Dan
ODonnell, Martin
Bertram, Lars
Roussel, Ronan
Luan, Jianan
Crosslin, David R.
Ward, Joey
Hansson, Markus
Hartwig, Fernando Pires
Chong, Michael
Dorr, Marcus
Ritchie, Marylyn D.
Pikhart, Hynek
Holliday, Elizabeth
Li, Ni
Padmanabhan, Sandosh
Houlston, Richard
McCarty, Catherine A.
Moldovan, Max
Langenberg, Claudia
Smart, Melissa
Snieder, Harold
Kinnersley, Ben
Cornish, Alex J.
Chasman, Daniel I.
van Iperen, Erik
Pell, Jill P.
Schmidt, Amand F.
Willeit, Johann
Morgan, Gareth
Humphries, Steve E.
Young, Robin
Whincup, Peter
Bonnefond, Amelie
Labreche, Karim
Volzke, Henry
Finan, Chris
Ridker, Paul M.
Wanamethee, Goya
Dale, Caroline
Went, Molly
Attia, John
Ben-Shlomo, Yoav
Hingorani, Aroon D.
Tamosiunas, Abdonas
van der Schouw, Yvonne T.
Seshadri, Sudha
Kumari, Meena
Carrell, David S.
Denny, Joshua C.
Maitland-van der Zee, Anke H.
Matullo, Giuseppe
Patel, Riyaz S.
Sacerdote, Carlotta
Sattar, Naveed
Norman, Kristina
Power, Christine
Ford, Ian
Pająk, Andrzej
Lind, Lars
Schofield, Peter
Yusuf6, Salim
Holmes, Michael V.
Baumeister, Sebastian
Volker, Uwe
Christophersen, Ingrid E.
Scott, Rodney
Onland-Moret, N. Charlotte
Allan, James
Weinhold, Niels
Nilsson, Bjorn
Steinhagen-Thiessen, Elisabeth
Preiss, David
Verweij, Niek
Coassin, Stefan
Cariou, Bertrand
Bobak, Martin
Sanson, Marc
Jess, Tine
Baranova, Ekaterina V.
Bots, Michiel L.
Kivimaki, Mika
Willeit, Karin
Thuillier, Dorothee
Sonneveld, Pieter
Hofman, Albert
Teumer, Alexander
Hypponen, Elina
Simon, Matthias
Sud, Amit
de Andrade, Mariza
Larson, Eric B.
Carty, Cara
Grarup, Niels
Reiner, Alex P.
Said, M. Abdullah
Marques-Vidal, Pedro
Demuth, Juri
Fatemifar, Ghazaleh
Keating, Brendan J.
Hemingway, Harry
van der Harst, Pim
Mook-Kanamori, D. O.
Dobbins, Sara E.
Kubinova, Ruzena
Horta, Bernardo Lessa
Dehghan, Abbas
Pedersen, Oluf
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Subsequent event risk in individuals with established coronary heart disease : design and rationale of the GENIUS-CHD consortium
Autorzy:
Sun, Yan
Delgado, Graciela
Carpeggiani, Clara
Pilbrow, Anna
Lee, Vei-Vei
Kofink, Daniel
Wallentin, Lars
Fox, Keith
Lang, Chim
Nikus, Kjell
Patel, Riyaz
Mahmoodi, B.
Simon, Tabassome
Gong, Yan
Pare, Guillaume
Al Ali, Lawien
Deloukas, Panos
Mons, Ute
James, Stefan
Laurikka, Jari
Szczeklik, Wojciech
ten Berg, Jurrien
Holmes, Michael
Kaminski, Karol
van der Graaf, Yolanda
Quyyumi, Arshed
Muehlschlegel, Jochen
Stender, Steen
Dube, Marie-Pierre
Stewart, Alexandre
Brenner, Hermann
Hartiala, Jaana
Hovingh, G.
Brugts, Jasper
Jukema, J.
Dudbridge, Frank
Richards, A.
Baranova, Ekaterina
Van de Werf, Frans
Scholz, Markus
Fitzpatrick, Natalie
Cresci, Sharon
Gijsberts, Crystel
Niemcunowicz-Janica, Anna
McPherson, Ruth
Lotufo, Paulo
Tang, W.H.
Drexel, Heinz
Alver, Maris
Danchin, Nicolas
Burkhardt, Ralph
Wilde, Arthur
Anderson, Jeffrey
McCubrey, Raymond
Marziliano, Nicola
Pereira, Alexandre
Pepine, Carl
Pilote, Louise
Saely, Christoph
Carlquist, John
Grobbee, Diederick
Kleber, Marcus
Direk, Kenan
Lindholm, Daniel
Martinelli, Nicola
Sandesara, Pratik
Ardissino, Diego
Girelli, Domenico
Leiherer, Andreas
Johnson, Julie
Bogaty, Peter
Lagerqvist, Bo
Lehtimaki, Terho
Arsenault, Benoit
Levin, Daniel
Bots, Michiel
Kaczor, Marcin
Doughty, Robert
Virani, Salim
Sinisalo, Juha
Siegbahn, Agneta
Boersma, Eric
Wauters, Els
Algra, Ale
Duarte, Nubia
Lokki, Marja-Liisa
Engert, James
Smith, J.
Schmidt, Amand
Trompet, Stella
Marz, Winfried
Kettner, Jiri
van Setten, Jessica
Hagstrom, Emil
Sanak, Marek
Boeckx, Bram
Lenzini, Petra
Klungel, Olaf
Cooper-DeHoff, Rhonda
Body, Simon
Kahonen, Mika
Hingorani, Aroon
Breitling, Lutz
van der Laan, Sander
Tragante, Vinicius
Pitha, Jan
Samman-Tahhan, Ayman
Szpakowicz, Anna
Nelson, Christopher
Tanck, Michael
Deanfield, John
Spertus, John
Held, Claes
Tfelt-Hansen, Jacob
Condorelli, Gianluigi
Horne, Benjamin
Ballantyne, Christie
Sattar, Naveed
Melander, Olle
Metspalu, Andres
Tardif, Jean-Claude
Visseren, Frank
Ford, Ian
Teren, Andrej
Allayee, Hooman
Waltenberger, Johannes
Foco, Luisa
Hoefer, Imo
Maitland-van der Zee, Anke
Jabbari, Reza
Muhlestein, Joseph
Akerblom, Axel
Kuukasjarvi, Pekka
Palmer, Colin
Stott, David
Engstrom, Thomas
Thanassoulis, George
Eriksson, Niclas
de Faire, Ulf
Hubacek, Jaroslav
Lambrechts, Diether
Hazen, Stanley
Boerwinkle, Eric
Glinge, Charlotte
Heydarpour, Mahyar
Pasterkamp, Gerard
Dufresne, Line
Bezzina, Connie
Newton-Cheh, Christopher
Behlouli, Hassan
Anselmi, Chiara
Casu, Gavino
Lyytikainen, Leo-Pekka
Leander, Karin
Vlachopoulou, Efthymia
Gigante, Bruna
Andreassi, Maria
Bergmeijer, Thomas
Cameron, Vicky
Asselbergs, Folkert
Kiliszek, Marek
Carruthers, Kathryn
Thiery, Joachim
Brophy, James
Braund, Peter
Fox, Kim
Almgren, Peter
Hemingway, Harry
Briguori, Carlo
Timmis, Adam
van der Harst, Pim
Opolski, Grzegorz
Samani, Nilesh
Vilmundarson, Ragnar
Howe, Laurence
Ploski, Rafal
Torp-Pedersen, Christian
Olivieri, Oliviero
Kotti, Salma
Opis:
BACKGROUND: The Genetics of Subsequent Coronary Heart Disease (GENIUS-CHD) consortium was established to facilitate discovery and validation of genetic variants and biomarkers for risk of subsequent CHD events, in individuals with established CHD. METHODS: The consortium currently includes 57 studies from 18 countries, recruiting 185 614 participants with either acute coronary syndrome, stable CHD, or a mixture of both at baseline. All studies collected biological samples and followed-up study participants prospectively for subsequent events. RESULTS: Enrollment into the individual studies took place between 1985 to present day with a duration of follow-up ranging from 9 months to 15 years. Within each study, participants with CHD are predominantly of self-reported European descent (38%-100%), mostly male (44%–91%) with mean ages at recruitment ranging from 40 to 75 years. Initial feasibility analyses, using a federated analysis approach, yielded expected associations between age (hazard ratio, 1.15; 95% CI, 1.14-1.16) per 5-year increase, male sex (hazard ratio, 1.17; 95% CI, 1.13-1.21) and smoking (hazard ratio, 1.43; 95% CI, 1.35-1.51) with risk of subsequent CHD death or myocardial infarction and differing associations with other individual and composite cardiovascular endpoints. CONCLUSIONS: GENIUS-CHD is a global collaboration seeking to elucidate genetic and nongenetic determinants of subsequent event risk in individuals with established CHD, to improve residual risk prediction and identify novel drug targets for secondary prevention. Initial analyses demonstrate the feasibility and reliability of a federated analysis approach. The consortium now plans to initiate and test novel hypotheses as well as supporting replication and validation analyses for other investigators.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Association of chromosome 9p21 with subsequent coronary heart disease events : a GENIUS-CHD study of individual participant data
Autorzy:
Kaminski, Karol A.
Allayee, Hooman
Boeckx, Bram
Kuukasjarvi, Pekka
Gijsberts, Crystel M.
Carlquist, John F.
Dube, Marie-Pierre
Leander, Karin
Hemingway, Harry
Hoefer, Imo E.
Stewart, Alexandre F.R.
Thanassoulis, George
Saely, Christoph H.
Held, Claes
Olivieri, Oliviero
Nelson, Christopher P.
Cresci, Sharon
Lee, Vei-Vei
Cooper-DeHoff, Rhonda M.
Kaczor, Marcin
Briguori, Carlo
Thiery, Joachim
Anderson, Jeffrey L.
Kleber, Marcus
Smith, J. Gustav
Burkhardt, Ralph
de Faire, Ulf
Leiherer, Andreas
Nikus, Kjell
Ford, Ian
Vlachopoulou, Efthymia
Almgren, Peter
Pilbrow, Anna P.
Body, Simon C.
Lang, Chim C.
Gigante, Bruna
ten Berg, Jurrien M.
Algra, Ale
Pitha, Jan
James, Stefan
Hartiala, Jaana
Eriksson, Niclas
Howe, Laurence J.
Direk, Kenan
Drexel, Heinz
Szpakowicz, Anna
Pare, Guillaume
Akerblom, Axel
Schmidt, Amand F.
Hubacek, Jaroslav A.
Sanak, Marek
Virani, Salim S.
Vilmundarson, Ragnar O.
Wilde, Arthur A.M.
Van de Werf, Frans J.
Pepinski, Witold
Waltenberger, Johannes
Arsenault, Benoit J.
Maitland-van der Zee, Anke H.
McPherson, Ruth
McCubrey, Raymond O.
Stott, David J.
Sattar, Naveed
Breitling, Lutz P.
Ploski, Rafal
Wauters, Els
Boerwinkle, Eric
Hazen, Stanley L.
Muhlestein, Joseph B.
Johnson, Julie A.
Kofink, Daniel
Spertus, John A.
Wallentin, Lars
Cheh, Chris Newton
Pereira, Alexandre C.
Lotufo, Paulo A.
Pilote, Louise
Gong, Yan
Bezzina, Connie R.
Melander, Olle
Condorelli, Gianluigi
Hovingh, G. Kees
Carpeggiani, Clara
Horne, Benjamin D.
Casu, Gavino
Hingorani, Aroon D.
Patel, Riyaz S.
Deloukas, Panos
Samman-Tahhan, Ayman
Dufresne, Line
Lyytikainen, Leo-Pekka
Ardissino, Diego
Brenner, Hermann
Ballantyne, Christie M.
Mordi, Ify R.
Sinisalo, Juha
Alver, Maris
Pasterkamp, Gerard
Holmes, Michael V.
Heydarpour, Mahyar
Opolski, Grzegorz
Carruthers, Kathryn F.
Laurikka, Jari O.
Siegbahn, Agneta
Girelli, Domenico
Mahmoodi, Bakhtawar K.
Marziliano, Nicola
Marz, Winfried
Behlouli, Hassan
Duarte, Nubia E.
Foco, Luisa
Fox, Keith A.A.
Trompet, Stella
van der Graaf, Yolanda
Visseren, Frank L.J.
Lagerqvist, Bo
Metspalu, Andres
Scholz, Markus
van der Harst, Pim
Cameron, Vicky A.
Wilson Tang, W.H.
de Borst, Gert J.
Mons, Ute
Tragante, Vinicius
Quyyumi, Arshed A.
Samani, Nilesh J.
Bergmeijer, Thomas O.
Palmer, Colin N.
Braund, Peter S.
Asselbergs, Folkert W.
Fitzpatrick, Natalie
Tardif, Jean-Claude
Pepine, Carl J.
Levin, Daniel
Richards, A. Mark
Doughty, Robert N.
Tanck, Michael W.T.
Lindholm, Daniel
de Jong, Pim A.
Brophy, James M.
Lambrechts, Diether
van der Laan, Sander W.
Anselmi, Chiara Viviani
Lenzini, Petra A.
Timmis, Adam
Muehlschlegel, Jochen D.
Jukema, J. Wouter
Hagstrom, Emil
van Setten, Jessica
Dudbridge, Frank
Baranova, Ekaterina V.
Lokki, Marja-Liisa
Sandesara, Pratik B.
Bogaty, Peter
Andreassi, Maria G.
Teren, Andrej
Deanfield, John
Martinelli, Nicola
Engert, James C.
Kahonen, Mika
Klungel, Olaf H.
Kiliszek, Marek
Delgado, Graciela
Kettner, Jiri
Lehtimaki, Terho
Szczeklik, Wojciech
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Wyświetlanie 1-10 z 12

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