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About the database ScholarIQanswers from OpenAlex & ORCID
How has Luisa De Sanctis's publication output changed over time?
ScholarIQpublication output · 1995–2025
Output grew0% over the shown period — from 1 works in 1995 to 1 in 2025.
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1995199920012002200520102016201820202025
What are the most-cited papers on Luisa De Sanctis?
ScholarIQmost cited works
Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology
A S Paul van Trotsenburg, Athanasia Stoupa, Juliane Léger, Tilman Rohrer, Catherine Peters, Laura Fugazzola, Alessandra Cassio, Claudine Heinrichs, Véronique Beauloye, Joachim Pohlenz, Patrice Rodien, R. Coutant, Gabor Szinnai, Philip Murray, Beate Bartès, Dominique Luton, Mariacarolina Salerno, Luisa De Sanctis, Mariacristina Vigone, Heiko Krude, Luca Persani, Michel Polak
Thyroid. 2020454 CitationsOPEN ACCESS
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
Giovanna Mantovani, Murat Bastepe, David Monk, Luisa De Sanctis, Susanne Thiele, Alessia Usardi, S. Faisal Ahmed, Roberto Bufo, Timothée Choplin, Gianpaolo De Filippo, Guillemette Devernois, Thomas Eggermann, Francesca Marta Elli, Kathleen Freson, Aurora García Ramirez, Emily L. Germain‐Lee, Lionel Groussin, Neveen A. T. Hamdy, Patrick Hanna, Olaf Hiort, Harald Jüppner, Peter Kamenický, Nina Knight, Marie-Laure Kottler, Elvire Le Norcy, Beatriz Lecumberri, Michael A. Levine, Outi Mäkitie, Regina Matsunaga Martin, Gabriel Ángel Martos‐Moreno, Masanori Minagawa, Philip Murray, Arrate Pereda, Robert J. Pignolo, Lars Rejnmark, Rebecca Rodado, Anya Rothenbühler, Vrinda Saraff, Ashley H. Shoemaker, Eileen M. Shore, Caroline Silve, Serap Turan, Philip R. Woods, M. Carola Zillikens, Guiomar Pérez de Nanclares, Agnès Linglart
S116269268. 2018345 CitationsOPEN ACCESS
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
Lídia Feliubadaló, Mariona Font, Jesús Purroy, F. Rousaud, Xavier Estivill, Virginia Nunes, Eliahu Golomb, Michael Centola, Ivona Aksentijevich, Yitshak Kreiss, Boleslaw Goldman, Mordechai Pras, Daniel L. Kastner, Elon Pras, Paolo Gasparini, Luigi Bisceglia, Ercole Beccia, Michele Gallucci, Luisa De Sanctis, Alberto Ponzone, Gian Franco Rizzoni, Leopoldo Zelante, Maria Teresa Bassi, Alfred L. George, Marta Manzoni, Alessandro De Grandi, Mirko Riboni, John K. Endsley, Andrea Ballabio, Giuseppe Borsani, Núria Reig, Esperanza Fernández, Raúl Estévez, Marta Pineda, David Torrents, Marta Camps, Jorge Lloberas, António Zorzano, Manuel Palacı́n
S137905309. 1999336 Citations
Comparison between SLC3A1 and SLC7A9 Cystinuria Patients and Carriers
Luca Dello Strologo, Elon Pras, C. Pontesilli, Ercole Beccia, Vittorino Ricci-Barbini, Luisa De Sanctis, Alberto Ponzone, Michele Gallucci, Luigi Bisceglia, Leopoldo Zelante, Maite Jiménez-Vidal, Mariona Font, António Zorzano, F. Rousaud, Virginia Nunes, Paolo Gasparini, Manuel Palaci[Combining Acute Accent]n, Gianfranco Rizzoni
Journal of the American Society of Nephrology. 2002278 Citations
<i>SOX2</i> anophthalmia syndrome
Nicola Ragge, Birgit Lorenz, Adele Schneider, Kate Bushby, Luisa De Sanctis, Ugo de Sanctis, Alison Salt, J. R. O. Collin, Anthony J. Vivian, S. L. Free, Pamela J. Thompson, Kathleen A. Williamson, Sanjay M. Sisodiya, Veronica van Heyningen, David Fitzpatrick
American Journal of Medical Genetics Part A. 2005228 Citations
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Institution
Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology
Paper
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
Paper
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
Paper
Comparison between SLC3A1 and SLC7A9 Cystinuria Patients and Carriers
Paper
<i>SOX2</i> anophthalmia syndrome
Paper