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Valentina Escott‐Price

ResearcherPublications, citations & collaboration network

Valentina Escott‐Price is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Valentina Escott‐Price have?

ScholarIQindexed works

Valentina Escott‐Price has 402 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Valentina Escott‐Price have?

ScholarIQcitation count

Valentina Escott‐Price has 52,905 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Valentina Escott‐Price?

ScholarIQh-index

Valentina Escott‐Price has an h-index of 86 in OpenAlex.

What is the i10-index of Valentina Escott‐Price?

ScholarIQi10-index

Valentina Escott‐Price has an i10-index of 201 in OpenAlex.

What is the ORCID of Valentina Escott‐Price?

ScholarIQorcid

The ORCID for Valentina Escott‐Price is on the source record.

What is the OpenAlex record for Valentina Escott‐Price?

ScholarIQopenalex

The OpenAlex for Valentina Escott‐Price is on the source record.

What are the most-cited papers on Valentina Escott‐Price?

ScholarIQmost cited works
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke, B M Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, H Huang, Menachem Fromer, Jacqueline I. Goldstein, Mark J. Daly, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberly D. Chambert, Giulio Genovese, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Steven A. McCarroll, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Tune H. Pers, J. N. Hirschhorn, Alkes Price, Eli Stahl, Esko T, Aiden Corvin, Paul Cormican, Gary Donohoe, Derek W. Morris, Michael Gill, James T. R. Walters, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Michael O‘Donovan, David A. Collier, Younes Mokrab, Ingrid Agartz, Erik Söderman, Erik G. Jönsson, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Esben Agerbo, Preben Bo Mortensen, Ditte Demontis, Thomas Folkmann Hansen, Manuel Mattheisen, Ole Mors, Line Olsen, H Kruuse Rasmussen, Anders D. Børglum, Werge Tm, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, S Bacanu, Tim B. Bigdeli, Bradley T. Webb, Brandon K. Wormley, Martin Begemann, Christian Hammer, Sergi Papiol, Hannelore Ehrenreich, Béné Jj, Béla Melegh, Anna K. Kähler, Patrik K. E. Magnusson, Christina M. Hultman, Patrick F. Sullivan, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Joshua L. Roffman, William Byerley, Wiepke Cahn, René S. Kahn, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Buxbaum Jn, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman
Nature. 20148,164 CitationsOPEN ACCESS
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen, Naomi R. Wray, 23andMe, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M. Byrne, Abdel Abdellaoui, Mark J. Adams, Esben Agerbo, Tracy Air, Till F. M. Andlauer, Silviu‐Alin Bacanu, Marie Bækvad‐Hansen, Aartjan T.F. Beekman, Tim B. Bigdeli, Elisabeth B. Binder, Douglas Blackwood, Julien Bryois, Henriette N. Buttenschøn, Jonas Bybjerg‐Grauholm, Na Cai, Enrique Castelao, Jane Christensen, Toni‐Kim Clarke, Jonathan R. I. Coleman, Lucía Colodro‐Conde, Baptiste Couvy‐Duchesne, Nick Craddock, Gregory E. Crawford, Cheynna Crowley, Hassan S. Dashti, Gail Davies, Ian J. Deary, Franziska Degenhardt, Eske M. Derks, Neşe Direk, Conor V. Dolan, Erin C. Dunn, Thalia C. Eley, Nicholas Eriksson, Valentina Escott‐Price, Farnush Hassan Farhadi Kiadeh, Hilary K. Finucane, Andreas J. Forstner, Josef Frank, Héléna A. Gaspar, Michael Gill, Paola Giusti‐Rodríguez, Fernando S. Goes, Scott D. Gordon, Jakob Grove, Lynsey S. Hall, Eilís Hannon, Christine Søholm Hansen, Thomas Folkmann Hansen, Stefan Herms, Ian B. Hickie, Per Hoffmann, Georg Homuth, Carsten Horn, Jouke‐Jan Hottenga, David M. Hougaard, Ming Hu, Craig Hyde, Marcus Ising, Rick Jansen, Fulai Jin, Eric Jorgenson, James A. Knowles, Isaac S. Kohane, Julia Kraft, Warren W. Kretzschmar, Jesper Krogh, Zoltán Kutalik, Jacqueline M. Lane, Yihan Li, Yun Li, Penelope A. Lind, Xiaoxiao Liu, Leina Lu, Donald J. MacIntyre, Dean F. MacKinnon, Robert Maier, Wolfgang Maier, Jonathan Marchini, Hamdi Mbarek, Patrick J. McGrath, Peter McGuffin, Sarah E. Medland, Divya Mehta, Christel M. Middeldorp, Evelin Mihailov, Yuri Milaneschi, Lili Milani, Jonathan Mill, Francis M. Mondimore, Grant W. Montgomery, Sara Mostafavi, Niamh Mullins
Nature Genetics. 20183,337 CitationsOPEN ACCESS
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela Tan, Demis A. Kia, Alastair J. Noyce, Angli Xue, José Brás, Emily Young, Rainer von Coelln, Javier Simón-Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Lasse Pihlstrøm, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Faraz Faghri, J Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Juan A. Botía, María Martínez, Jean‐Christophe Corvol, Suzanne Lesage, Joseph Jankovic, Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew B Singleton, Astrid Adarmes‐Gómez, Miquel Aguilar, Akbota Aitkulova, Vadim Akhmetzhanov, Roy N. Alcalay, Ignacio Álvarez, Victoria Álvarez, Sara Bandrés‐Ciga, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Kimberley J. Billingsley, Cornelis Blauwendraat, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, José Brás, Alexis Brice, Kathrin Brockmann, Vivien J. Bubb, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Viorica Chelban, Jordi Clarimón, Carl E Clarke, Yaroslau Compta, Mark Cookson, Jean‐Christophe Corvol, David W. Craig, Fabrice Danjou, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, Raquel Durán, Francisco Escamilla‐Sevilla, Valentina Escott‐Price, Mario Ezquerra, Faraz Faghri, Cici Feliz, Manel Fernández, Rubén Fernández‐Santiago, Steven Finkbeiner, Thomas Foltynie, Ziv Gan‐Or, Ciara García
The Lancet Neurology. 20192,577 CitationsOPEN ACCESS
Analysis of shared heritability in common disorders of the brain
Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Raymond K. Walters, José Brás, Laramie E. Duncan, Valentina Escott‐Price, Guido J. Falcone, Padhraig Gormley, Rainer Malik, Nikolaos A. Patsopoulos, Stephan Ripke, Zhi Wei, Dongmei Yu, Phil H. Lee, Patrick Turley, Benjamin Grenier‐Boley, Vincent Chouraki, Yoichiro Kamatani, Claudine Berr, Luc Letenneur, Didier Hannequin, Philippe Amouyel, Anne Boland, Jean‐François Deleuze, Emmanuelle Duron, Badri N. Vardarajan, Christiane Reitz, Alison Goate, Matthew J. Huentelman, M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte
Science. 20182,047 CitationsOPEN ACCESS
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Antonio F. Pardiñas, Peter Holmans, Andrew Pocklington, Valentina Escott‐Price, Stephan Ripke, Noa Carrera, Sophie E. Legge, Sophie Bishop, Darren Cameron, Marian L. Hamshere, Jun Han, Leon Hubbard, Amy Lynham, Kiran K. Mantripragada, Elliott Rees, James H. MacCabe, Steven A. McCarroll, Bernhard T. Baune, Gerome Breen, Enda M. Byrne, Udo Dannlowski, Thalia C. Eley, Caroline Hayward, Nicholas G. Martin, Andrew M. McIntosh, Robert Plomin, David J. Porteous, Naomi R. Wray, Armando Caballero, Daniel H. Geschwind, Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O‘Donovan, James Walters
Nature Genetics. 20181,745 CitationsOPEN ACCESS

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