ScholarIQanswers from OpenAlex
Centre for Biomedical Network Research on Rare Diseases
InstitutionResearch output, impact & collaborations
Centre for Biomedical Network Research on Rare Diseases is a institution indexed in ScholarIQ from OpenAlex.
What is known about Centre for Biomedical Network Research on Rare Diseases?
ScholarIQrecord summary
Centre for Biomedical Network Research on Rare Diseases is a research organisation in Madrid, ES. OpenAlex records 13,828 works and 1,344,140 citations for it. 2,565 researchers list it as their most recent affiliation.
How many works does Centre for Biomedical Network Research on Rare Diseases have?
ScholarIQindexed works
Centre for Biomedical Network Research on Rare Diseases has 13,828 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Centre for Biomedical Network Research on Rare Diseases have?
ScholarIQcitation count
Centre for Biomedical Network Research on Rare Diseases has 1,344,140 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Centre for Biomedical Network Research on Rare Diseases?
ScholarIQresearcher count
Centre for Biomedical Network Research on Rare Diseases has 2,565 researchers in the ScholarIQ index.
What is the average h-index at Centre for Biomedical Network Research on Rare Diseases?
ScholarIQavg h-index
Centre for Biomedical Network Research on Rare Diseases has an average h-index of 66 in OpenAlex.
What is the ROR of Centre for Biomedical Network Research on Rare Diseases?
ScholarIQror
The ROR for Centre for Biomedical Network Research on Rare Diseases is on the source record.
What is the OpenAlex record for Centre for Biomedical Network Research on Rare Diseases?
ScholarIQopenalex
The OpenAlex for Centre for Biomedical Network Research on Rare Diseases is on the source record.
Who are the most-cited researchers behind Centre for Biomedical Network Research on Rare Diseases?
ScholarIQtop researchers by citations
What are the most-cited papers on Centre for Biomedical Network Research on Rare Diseases?
ScholarIQmost cited works
Risks of Breast, Ovarian, and Contralateral Breast Cancer for <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers
Karoline Kuchenbaecker, John L. Hopper, Daniel R. Barnes, Kelly‐Anne Phillips, Thea M. Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E. van Leeuwen, Roger L. Milne, Nadine Andrieu, David E. Goldgar, Mary Beth Terry, Matti A. Rookus, Douglas F. Easton, Antonis C. Antoniou, Lesley McGuffog, D. Gareth Evans, Daniel Barrowdale, Debra Frost, Julian Adlard, Kai-Ren Ong, Louise Izatt, Marc Tischkowitz, Rosalind A. Eeles, Rosemarie Davidson, Shirley Hodgson, Steve Ellis, Catherine Noguès, Christine Lasset, Dominique Stoppa‐Lyonnet, Jean‐Pierre Fricker, Laurence Faivre, Pascaline Berthet, Maartje J. Hooning, Lizet E. van der Kolk, Carolien M. Kets, Muriel A. Adank, Esther M. John, Wendy K. Chung, Irene L. Andrulis, Melissa C. Southey, Mary B. Daly, Saundra S. Buys, Ana Osório, Christoph Engel, Karin Kast, Rita K. Schmutzler, Trinidad Caldés, Anna Jakubowska, Jacques Simard, Michael Friedländer, Sue‐Anne McLachlan, Eva Macháčková, Lenka Foretová, Yen Y. Tan, Christian F. Singer, Edith Oláh, Anne‐Marie Gerdes, Brita Arver, Håkan Olsson
The IASLC Lung Cancer Staging Project
Wilfried Eberhardt, Alan Mitchell, John Crowley, Haruhiko Kondo, Young Tae Kim, Andrew T. Turrisi, Peter Goldstraw, Ramón Rami–Porta
Challenges and perspectives in obstructive sleep apnoea
Winfried Randerath, Claudio L. Bassetti, Maria R. Bonsignore, Ramón Farré, Luigi Ferini‐Strambi, Ludger Grote, Jan Hedner, Malcolm Kohler, Miguel Ángel Martínez‐García, Ștefan Mihăicuță, Josep M. Montserrat, Jean‐Louis Pépin, Dirk Pevernagie, Fabio Pizza, Olli Polo, Renata L. Riha, Silke Ryan, Johan Verbraecken, Walter T. McNicholas
Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer
Christopher A. Maxwell, Javier Benítez, Laia Gómez‐Baldó, Ana Osório, Núria Bonifaci, Ricardo Fernández‐Ramires, Sylvain V. Costes, Elisabet Guinó, Helen Chen, Gareth J. R. Evans, Pooja Mohan, Isabel Català, Anna Petit, Helena Aguilar, Alberto Villanueva, Àlvaro Aytés, Jordi Serra-Musach, Gad Rennert, Flavio Lejbkowicz, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Carla B. Ripamonti, Bernardo Bonanni, Alessandra Viel, Anna Allavena, Loris Bernard, Paolo Radice, Eitan Friedman, Bella Kaufman, Yael Laitman, Maya Dubrovsky, Roni Milgrom, Anna Jakubowska, Cezary Cybulski, Bohdan Górski, Katarzyna Jaworska, Katarzyna Durda, Grzegorz Sukiennicki, Jan Lubiński, Yin Yao Shugart, Susan M. Domchek, Richard Letrero, Barbara L. Weber, Frans B.L. Hogervorst, Matti A. Rookus, J. Margriet Collée, Peter Devilee, Marjolijn J. L. Ligtenberg, Rob B. van der Luijt, Cora M. Aalfs, Quinten Waisfisz, Juul Wijnen, C. E. P. van Roozendaal, HEBON, EMBRACE, Douglas F. Easton, Susan Peock, Margaret Cook, Clare Oliver, Debra Frost, Patricia Harrington, D. Gareth Evans, Fiona Lalloo, Rosalind A. Eeles, Louise Izatt, Carol Chu, Diana Eccles, Fiona Douglas, Carole Brewer, Heli Nevanlinna, Tuomas Heikkinen, Fergus J. Couch, Noralane M. Lindor, Xianshu Wang, Andrew K. Godwin, Maria A. Caligo, Grazia Lombardi, Niklas Loman, Per Karlsson, Hans Ehrencrona, Anna von Wachenfeldt, SWE-BRCA, Rósa B. Barkardóttir, Ute Hamann, Muhammad Usman Rashid, Adriana Lasa, Trinidad Caldés, Raquel Andrés, Michael Schmitt, Volker Assmann, Kristen N. Stevens, Kenneth Offit, João Curado, Hagen Tilgner, Roderic Guigó, Gemma Aiza, Joan Brunet, Joan Castellsagué, Griselda Martrat
Prediction of Breast and Prostate Cancer Risks in Male <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers Using Polygenic Risk Scores
Julie Lecarpentier, Valentina Silvestri, Karoline Kuchenbaecker, Daniel Barrowdale, Joe Dennis, Lesley McGuffog, Penny Soucy, Goska Leslie, Piera Rizzolo, Anna Sara Navazio, Virginia Valentini, Veronica Zelli, Andrew Lee, Ali Amin Al Olama, Jonathan P. Tyrer, Melissa C. Southey, Esther M. John, Thomas Conner, David E. Goldgar, Saundra S. Buys, Ramūnas Janavičius, Linda Steele, Yuan Chun Ding, Susan L. Neuhausen, Thomas van Overeem Hansen, Ana Osório, Jeffrey N. Weitzel, Angela Toss, Veronica Medici, Laura Cortesi, Ines Zanna, Domenico Palli, Paolo Radice, Siranoush Manoukian, Bernard Peissel, Jacopo Azzollini, Alessandra Viel, Giulia Cini, Giuseppe Damante, Stefania Tommasi, Paolo Peterlongo, Florentia Fostira, Ute Hamann, D. Gareth Evans, Alex Henderson, Carole Brewer, Diana Eccles, Jackie Cook, Kai-Ren Ong, Lisa Walker, Lucy Side, Mary Porteous, Rosemarie Davidson, Shirley Hodgson, Debra Frost, Julian Adlard, Louise Izatt, Rosalind A. Eeles, Steve Ellis, Marc Tischkowitz, EMBRACE, Andrew K. Godwin, Alfons Meindl, Andrea Gehrig, Bernd Dworniczak, Christian Sutter, Christoph Engel, Dieter Niederacher, Doris Steinemann, Eric Hahnen, Jan Hauke, Kerstin Rhiem, Karin Kast, Norbert Arnold, Nina Ditsch, Shan Wang‐Gohrke, Barbara Wappenschmidt, Dorothea Wand, Christine Lasset, Dominique Stoppa‐Lyonnet, Muriel Belotti, Francesca Damiola, Laure Barjhoux, Sylvie Mazoyer, GEMO Study Collaborators, Mattias Van Heetvelde, Bruce Poppe, Kim De Leeneer, Kathleen Claes, Miguel de la Hoya, Vanesa García‐Barberán, Trinidad Caldes, Pedro Pérez Segura, Johanna I. Kiiski, Kristiina Aittomäki, Sofia Khan, Heli Nevanlinna, Christi J. van Asperen, HEBON, Vaszko Tibor
How much of the research on Centre for Biomedical Network Research on Rare Diseases is open access?
ScholarIQopen access share
100%OPEN ACCESS