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1
Modification of kidney barrier function by the urokinase receptor
Modification of kidney barrier function by the urokinase receptor
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Modification of kidney barrier function by the urokinase receptor

Zacchigna, Serena ; Xie, Liang ; Schmid, Holger ; Bendayan, Moïse ; Mundel, Peter ; Li, Jing ; Rastaldi, Maria P ; Kretzler, Matthias ; Henger, Anna ; Altintas, Mehmet M ; Nikolic, Boris ; Reiser, Jochen ; Schwarz, Karin ; Cowan, Peter ; Parrilla, Roberto ; Möller, Clemens C ; Wei, Changli ; Carmeliet, Peter ; Gupta, Vineet ; Kalluri, Raghu

Nature medicine, 2008-01, Vol.14 (1), p.55-63 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Frequency combs induced by phase turbulence
Frequency combs induced by phase turbulence
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Frequency combs induced by phase turbulence

Piccardo, Marco ; Schwarz, Benedikt ; Kazakov, Dmitry ; Beiser, Maximilian ; Opačak, Nikola ; Wang, Yongrui ; Jha, Shantanu ; Hillbrand, Johannes ; Tamagnone, Michele ; Chen, Wei Ting ; Zhu, Alexander Y ; Columbo, Lorenzo L ; Belyanin, Alexey ; Capasso, Federico

Nature (London), 2020-06, Vol.582 (7812), p.360-364 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Epidemiology and causes of preterm birth
Epidemiology and causes of preterm birth
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Epidemiology and causes of preterm birth

Goldenberg, Robert L, Prof ; Culhane, Jennifer F, PhD ; Iams, Jay D, Prof ; Romero, Roberto, Prof

The Lancet (British edition), 2008-01, Vol.371 (9606), p.75-84 [Periódico revisado por pares]

England: Elsevier Ltd

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4
A Spanish pillbox app for elderly patients taking multiple medications: randomized controlled trial
A Spanish pillbox app for elderly patients taking multiple medications: randomized controlled trial
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A Spanish pillbox app for elderly patients taking multiple medications: randomized controlled trial

Mira, José Joaquín ; Navarro, Isabel ; Botella, Federico ; Borrás, Fernando ; Nuño-Solinís, Roberto ; Orozco, Domingo ; Iglesias-Alonso, Fuencisla ; Pérez-Pérez, Pastora ; Lorenzo, Susana ; Toro, Nuria

Journal of medical Internet research, 2014-04, Vol.16 (4), p.e99-e99 [Periódico revisado por pares]

Canada: Journal of Medical Internet Research

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5
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

van Rheenen, Wouter ; Bakker, Mark K ; van Vugt, Joke J F A ; de Klein, Niek ; Westra, Harm-Jan ; Bakker, Olivier B ; Deelen, Patrick ; Hannon, Eilis ; Dolzhenko, Egor ; Gawor, Klara ; Westeneng, Henk-Jan ; Kooyman, Maarten ; Heverin, Mark ; Shatunov, Aleksey ; Ticozzi, Nicola ; Cooper-Knock, Johnathan ; Gromicho, Marta ; Chandran, Siddharthan ; Pal, Suvankar ; Shaw, Pamela J ; Hardy, John ; Orrell, Richard W ; Meyer, Thomas ; Lauria, Giuseppe ; Cereda, Cristina ; Sproviero, Daisy ; D'Alfonso, Sandra ; Sorarù, Gianni ; Siciliano, Gabriele ; Filosto, Massimiliano ; Padovani, Alessandro ; Calvo, Andrea ; Canosa, Antonio ; Grassano, Maurizio ; Beghi, Ettore ; Logroscino, Giancarlo ; Nefussy, Beatrice ; Lerner, Yossef ; Gotkine, Marc ; Baloh, Robert H ; Bell, Shaughn ; Vourc'h, Patrick ; Couratier, Philippe ; Salachas, François ; Assialioui, Abdelilah ; Dion, Patrick A ; Ross, Jay P ; Brenner, David ; Freischmidt, Axel ; Bensimon, Gilbert ; Brice, Alexis ; Saker-Delye, Safa ; Wood, Nicholas W ; Topp, Simon ; Lieb, Wolfgang ; Franke, Andre ; Ripke, Stephan ; Braun, Alice ; Hofman, Albert ; Cichon, Sven ; Nöthen, Markus M ; Traynor, Bryan J ; Singleton, Andrew B ; Mitne Neto, Miguel ; Ophoff, Roel A ; Wiedau-Pazos, Martina ; Lomen-Hoerth, Catherine ; Grosskreutz, Julian ; Gaur, Nayana ; Ilse, Benjamin ; Stubendorff, Beatrice ; Hübner, Christian A ; Graff, Caroline ; Fominykh, Vera ; Demeshonok, Vera ; Rogelj, Boris ; Zidar, Janez ; Ravnik-Glavač, Metka ; Drory, Vivian ; Povedano, Monica ; Blair, Ian P ; Kiernan, Matthew C ; McCombe, Pamela A ; Pamphlett, Roger ; Steyn, Frederik J ; de Carvalho, Mamede ; Petri, Susanne ; Weber, Markus ; Brown, Jr, Robert H ; Shaw, Christopher E ; Andersen, Peter M ; Groen, Ewout J N ; Garton, Fleur C ; Mill, Jonathan ; Hardiman, Orla ; Tsai, Ellen ; Runz, Heiko ; Al-Chalabi, Ammar ; van den Berg, Leonard H ; Veldink, Jan H

Nature genetics, 2021-12, Vol.53 (12), p.1636-1648 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Preterm Birth 1 Epidemiology and causes of preterm birth
Preterm Birth 1 Epidemiology and causes of preterm birth
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Preterm Birth 1 Epidemiology and causes of preterm birth

GOLDENBERG, Robert L ; CULHANE, Jennifer F ; LAMS, Jay D ; ROMERO, Roberto

The Lancet (British edition), 2008-01, Vol.371 (9606), p.75-84 [Periódico revisado por pares]

London: Lancet

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7
Geospatial immune variability illuminates differential evolution of lung adenocarcinoma
Geospatial immune variability illuminates differential evolution of lung adenocarcinoma
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Geospatial immune variability illuminates differential evolution of lung adenocarcinoma

AbdulJabbar, Khalid ; Raza, Shan E Ahmed ; Rosenthal, Rachel ; Jamal-Hanjani, Mariam ; Veeriah, Selvaraju ; Akarca, Ayse ; Lund, Tom ; Moore, David A ; Salgado, Roberto ; Al Bakir, Maise ; Zapata, Luis ; Hiley, Crispin T ; Officer, Leah ; Sereno, Marco ; Smith, Claire Rachel ; Loi, Sherene ; Hackshaw, Allan ; Marafioti, Teresa ; Quezada, Sergio A ; McGranahan, Nicholas ; Le Quesne, John ; Swanton, Charles ; Yuan, Yinyin

Nature medicine, 2020-07, Vol.26 (7), p.1054-1062 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
The evolution of lung cancer and impact of subclonal selection in TRACERx
The evolution of lung cancer and impact of subclonal selection in TRACERx
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The evolution of lung cancer and impact of subclonal selection in TRACERx

Frankell, Alexander M ; Dietzen, Michelle ; Al Bakir, Maise ; Lim, Emilia L ; Karasaki, Takahiro ; Ward, Sophia ; Veeriah, Selvaraju ; Colliver, Emma ; Huebner, Ariana ; Bunkum, Abigail ; Hill, Mark S ; Grigoriadis, Kristiana ; Moore, David A ; Black, James R M ; Liu, Wing Kin ; Thol, Kerstin ; Pich, Oriol ; Watkins, Thomas B K ; Naceur-Lombardelli, Cristina ; Cook, Daniel E ; Salgado, Roberto ; Wilson, Gareth A ; Bailey, Chris ; Angelova, Mihaela ; Bentham, Robert ; Martínez-Ruiz, Carlos ; Abbosh, Christopher ; Nicholson, Andrew G ; Le Quesne, John ; Biswas, Dhruva ; Rosenthal, Rachel ; Puttick, Clare ; Hessey, Sonya ; Lee, Claudia ; Prymas, Paulina ; Toncheva, Antonia ; Smith, Jon ; Xing, Wei ; Nicod, Jerome ; Price, Gillian ; Kerr, Keith M ; Naidu, Babu ; Middleton, Gary ; Blyth, Kevin G ; Fennell, Dean A ; Forster, Martin D ; Lee, Siow Ming ; Falzon, Mary ; Hewish, Madeleine ; Shackcloth, Michael J ; Lim, Eric ; Benafif, Sarah ; Russell, Peter ; Boleti, Ekaterini ; Krebs, Matthew G ; Lester, Jason F ; Papadatos-Pastos, Dionysis ; Ahmad, Tanya ; Thakrar, Ricky M ; Lawrence, David ; Navani, Neal ; Janes, Sam M ; Dive, Caroline ; Blackhall, Fiona H ; Summers, Yvonne ; Cave, Judith ; Marafioti, Teresa ; Herrero, Javier ; Quezada, Sergio A ; Peggs, Karl S ; Schwarz, Roland F ; Van Loo, Peter ; Miedema, Daniël M ; Birkbak, Nicolai J ; Hiley, Crispin T ; Hackshaw, Allan ; Zaccaria, Simone ; Jamal-Hanjani, Mariam ; McGranahan, Nicholas ; Swanton, Charles

Nature (London), 2023-04, Vol.616 (7957), p.525-533 [Periódico revisado por pares]

England: Nature Publishing Group

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9
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

Muona, Mikko ; Berkovic, Samuel F ; Dibbens, Leanne M ; Oliver, Karen L ; Maljevic, Snezana ; Bayly, Marta A ; Joensuu, Tarja ; Canafoglia, Laura ; Franceschetti, Silvana ; Michelucci, Roberto ; Markkinen, Salla ; Heron, Sarah E ; Hildebrand, Michael S ; Andermann, Eva ; Andermann, Frederick ; Gambardella, Antonio ; Tinuper, Paolo ; Licchetta, Laura ; Scheffer, Ingrid E ; Criscuolo, Chiara ; Filla, Alessandro ; Ferlazzo, Edoardo ; Ahmad, Jamil ; Ahmad, Adeel ; Baykan, Betul ; Said, Edith ; Topcu, Meral ; Riguzzi, Patrizia ; King, Mary D ; Ozkara, Cigdem ; Andrade, Danielle M ; Engelsen, Bernt A ; Crespel, Arielle ; Lindenau, Matthias ; Lohmann, Ebba ; Saletti, Veronica ; Massano, João ; Privitera, Michael ; Espay, Alberto J ; Kauffmann, Birgit ; Duchowny, Michael ; Møller, Rikke S ; Straussberg, Rachel ; Afawi, Zaid ; Ben-Zeev, Bruria ; Samocha, Kaitlin E ; Daly, Mark J ; Petrou, Steven ; Lerche, Holger ; Palotie, Aarno ; Lehesjoki, Anna-Elina

Nature genetics, 2015-01, Vol.47 (1), p.39-46 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Genome-wide analyses identify common variants associated with macular telangiectasia type 2
Genome-wide analyses identify common variants associated with macular telangiectasia type 2
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Genome-wide analyses identify common variants associated with macular telangiectasia type 2

Scerri, Thomas S ; Quaglieri, Anna ; Cai, Carolyn ; Zernant, Jana ; Matsunami, Nori ; Baird, Lisa ; Scheppke, Lea ; Bonelli, Roberto ; Yannuzzi, Lawrence A ; Friedlander, Martin ; Egan, Catherine A ; Fruttiger, Marcus ; Leppert, Mark ; Allikmets, Rando ; Bahlo, Melanie

Nature genetics, 2017-04, Vol.49 (4), p.559-567 [Periódico revisado por pares]

United States: Nature Publishing Group

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