ScholarIQanswers from OpenAlex & ORCID
Elvira Bramon
ResearcherPublications, citations & collaboration network
Elvira Bramon is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Elvira Bramon have?
ScholarIQindexed works
Elvira Bramon has 341 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Elvira Bramon have?
ScholarIQcitation count
Elvira Bramon has 37,751 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Elvira Bramon?
ScholarIQh-index
Elvira Bramon has an h-index of 72 in OpenAlex.
What is the i10-index of Elvira Bramon?
ScholarIQi10-index
Elvira Bramon has an i10-index of 179 in OpenAlex.
What is the ORCID of Elvira Bramon?
ScholarIQorcid
The ORCID for Elvira Bramon is on the source record.
What is the OpenAlex record for Elvira Bramon?
ScholarIQopenalex
The OpenAlex for Elvira Bramon is on the source record.
What are the most-cited papers on Elvira Bramon?
ScholarIQmost cited works
Large recurrent microdeletions associated with schizophrenia
GROUP, Hreinn Stefánsson, Dan Rujescu, Sven Cichon, Olli Pietiläinen, Andrés Ingason, Stacy Steinberg, Ragnheiður Fossdal, Engilbert Sigurðsson, Thordur Sigmundsson, Jacobine E. Buizer‐Voskamp, Thomas Folkmann Hansen, Klaus D. Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M. Matthews, Arnaldur Gylfason, Bjarni V. Halldórsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Björnsson, Sigurborg Mattiasdottir, Thórarinn Blöndal, Magnús Haraldsson, Brynja B. Magnúsdóttir, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Stephan Ripke, Colm Ó'Dúshláine, Kimberly Chambert, Jennifer L. Moran, Anna K. Kähler, Susanne Akterin, Sarah E. Bergen, Ann L. Collins, James J Crowley, Menachem Fromer, Yunjung Kim, Sang Lee, Patrik K. E. Magnusson, Nick Sanchez, Eli A. Stahl, Stephanie Williams, Naomi R. Wray, Kai Xia, Francesco Bettella, Anders D. Børglum, Brendan Bulik‐Sullivan, Paul Cormican, Nick Craddock, Christiaan de Leeuw, Naser Durmishi, Michael Gill, В. Е. Голимбет, Marian L. Hamshere, Peter Holmans, David M Hougaard, Kenneth S. Kendler, Kuang Lin, Derek W. Morris, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, F. Anthony O’Neill, Michael J. Owen, Milica Pejovic Milovancevic, Daniëlle Posthuma, John Powell, Alexander Richards, Brien P. Riley, Douglas M. Ruderfer, Dan Rujescu, Engilbert Sigurðsson, Teimuraz Silagadze, August B. Smit, Hreinn Stefánsson, Stacy Steinberg, Jaana Suvisaari, Sarah Tosato, Matthijs Verhage, James Walters, Elvira Bramon, Aiden Corvin, Michael O‘Donovan, Kari Stefansson, Edward M. Scolnick, Shaun Purcell, Steven A. McCarroll, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Amy Strange, Chris C. A. Spencer, Gavin Band, Céline Bellenguez, Colin L. Freeman, Matti Pirinen, Anna Rautanen, Zhan Su, Peter Donnelly, Francesca Capon, Jo Knight, Michael E. Weale, Michael H. Allen, Christopher G. Mathew, Frank O. Nestlé, Alexandros Onoufriadis, Catherine Smith, Jonathan N Barker, Richard C. Trembath, Anne Barton, Jane Worthington, Judith G.M. Bergboer, Joost Schalkwijk, Patrick L.J.M. Zeeuwen, Jenefer M. Blackwell, Elvira Bramon, Suzannah J. Bumpstead, Panos Deloukas, Sarah Edkins, Emma Gray, Sarah Hunt, Cordelia Langford, Simon Potter, Leena Peltonen, Juan P. Casas, Michael J. Cork, Rachid Tazi‐Ahnini, Aiden Corvin, Alexander Dilthey, Stephen Leslie, Loukas Moutsianas, Gilean McVean, Audrey Duncanson, Xavier Estivill, Eva Riveira‐Muñoz, Oliver FitzGerald, Brian Kirby, Emiliano Giardina, Giuseppe Novelli, Angelika Hofer, Wolfgang Salmhofer, Wolfgang Weger, Ulrike Hüffmeier, André Reis, Alan D. Irvine, Janusz Jankowski, Jesús Lascorz, Joyce Leman, A. David Burden, Lotus Mallbris, Mona Ståhle, Katarina Wolk, Hugh S. Markus, W.H. Irwin McLean, Ross McManus, Anthony W. Ryan, Rotraut Mößner, Åsa Torinsson Naluai, Lena Samuelsson, Colin N A Palmer, Carlo Perricone, R Plomin, Ramón M. Pujol, Stephen Sawcer, Adrian Hayday, Heiko Traupe, Ananth C. Viswanathan, Richard B Warren, Helen Young, Christopher E M Griffiths, Nicholas Wood, Juha Kere, David M. Evans, Matthew A. Brown
Disruption of the neurexin 1 gene is associated with schizophrenia
Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Folkmann Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, GROUP Investigators, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Folkmann Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, GROUP Investigators, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, Laura‐Maria Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair