Torthaí cuardaigh - Claudia Ciaccio
- 1 - 3 toradh as 3 á dtaispeáint
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Fragile X syndrome: a review of clinical and molecular diagnoses de réir Claudia Ciaccio, Laura Fontana, Donatella Milani, Silvia Tabano, Monica Miozzo, Susanna Esposito
Foilsithe / Cruthaithe 2017Revisão -
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PEDIA: prioritization of exome data by image analysis de réir Tzung‐Chien Hsieh, Martin A. Mensah, Jean Tori Pantel, Dione Aguilar, Omri Bar, Allan Bayat, Luis E. Becerra-Solano, Heidi Beate Bentzen, Saskia Biskup, Oleg Borisov, Øivind Braaten, Claudia Ciaccio, Marie Coutelier, Kirsten Cremer, Magdalena Danyel, Svenja Daschkey, Hilda David Eden, Koenraad Devriendt, Sandra Wilson, Sofia Douzgou, Dejan Đukić, Nadja Ehmke, Christine Fauth, Björn Fischer‐Zirnsak, Nicole Fleischer, Heinz Gabriel, Luitgard Graul‐Neumann, Karen W. Gripp, Yaron Gurovich, А.А. Гусина, Nechama Haddad, Nurulhuda Hajjir, Yair Hanani, Jakob Hertzberg, Konstanze Hoertnagel, Janelle Howell, Ivan Ivanovski, Angela M. Kaindl, Tom Kamphans, Susanne Kamphausen, Catherine Karimov, Hadil Kathom, Anna Keryan, Alexej Knaus, Sebastian Köhler, Uwe Kornak, А. В. Лавров, Maximilian Leitheiser, Gholson J. Lyon, Elisabeth Mangold, Purificación Marín Reina, Antonio Martínez Carrascal, Diana Mitter, Laura Morlán Herrador, Guy Nadav, Markus M. Nöthen, Alfredo Orrico, Claus‐Eric Ott, Kristen Park, Borut Peterlin, Laura Pölsler, Annick Raas‐Rothschild, Linda M. Randolph, Nicole Revençu, Christina Fagerberg, Peter Nick Robinson, Stanislav Rosnev, Sabine Rudnik, Goražd Rudolf, Ulrich A. Schatz, Anna Schossig, Max Schubach, Or Shanoon, Eamonn Sheridan, Pola Smirin‐Yosef, Malte Spielmann, Eun-Kyung Suk, Yves Sznajer, Christian T. Thiel, Gundula Thiel, Alain Verloès, Irena Vrečar, Dagmar Wahl, Ingrid Weber, Korina Winter, Marzena Wiśniewska, Bernd Wollnik, Ming Wai Yeung, Max Zhao, Na Zhu, Johannes Zschocke, Stefan Mundlos, Denise Horn, Peter Krawitz
Foilsithe / Cruthaithe 2019Artigo -
3
Risk of Major Congenital Malformations and Exposure to Antiseizure Medication Monotherapy de réir Dina Battino, Torbjörn Tomson, Erminio Bonizzoni, John Craig, Emilio Perucca, Anne Sabers, Sanjeev V. Thomas, Silje Alvestad, Piero Perucca, Frank Vajda, Chiara Pantaleoni, Claudia Ciaccio, Silvia Kochen, Frank Vajda, Gerhard Luef, Alejandro de Marinis, Jana Zárubová, Anne Sabers, Reetta Kälviäinen, Sofia Kasradze, Bettina Schmitz, Sanjeev V. Thomas, Nasim Tabrizi, Lilach Goldstein, Barbara Mostacci, Hideyuki Ohtani, Gordana Kiteva‐Trenchevska, Eugène van Puijenbroek, Silje Alvestad, Maja Milovanović, Vladimír Šafčák, Meritxell Martínez Ferri, Torbjörn Tomson, Elisabeth Sellitto, Hsiang‐Yu Yu, Stephanie Hödl, Petr Marusič, Renata Listonova, Hana Krijtová, David Franc, Petr Bušek, Michaela Kajšová, Noémi Becser Andersen, Birthe Pedersen, Katarzyna Maria Mieszczanek, Katarzyna Cebula, Stefan Juhl, Birgitte Forsom Sondal, Karen Nielsen, Tatiana V. Danielsen, Elsebeth Bruun Christiansen, Jakob Christensen, Ovidio Solano Cabrera, Aleksei Rakitin, Anne Kirss, Anna Maija Saukkonen, Nino Gogatishvili, Dieter Dennig, Kerstin Erdmann, Christian Dippon, Bernhard J. Steinhoff, Lisa Langenbruch, Holger Lerche, Anja Herzer, Jan S. Gerdes, Elisa K. El-Allawy-Zielke, Hajo M. Hamer, Malgorzata Kalita, Martin Hirsch, Stephan Arnold, Hans‐Beatus Straub, Rebekka Lehmann, Christiane Asenbauer, Florian Losch, Wenke Grönheit, Matthias Lindenau, Ramshekhar N. Menon, Jafar Mehvari Habibabadi, Maria Paola Canevini, Elena Zambrelli, Katherine Turner, Michela Cecconi, A Paggi, Nicoletta Foschi, Antonio Gambardella, Simone Beretta, Angela Giglio, Gaia Fanella, Lorenzo Ferri, Francesca Bisulli, Alessandra Pistelli, Pietro Pignatta, Marta Maschio, Francesca Muzzi, Maria Sofia Cotelli, Etsuko Yamazaki, Kiyohito Terada, Yushi Inoue, Masahiro Mizobuchi, Katsuyuki Fukushima
Foilsithe / Cruthaithe 2024Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Pediatrics
Artificial intelligence
Bioinformatics
Cohort study
Computational biology
Computer science
Confounding
Database
Disease
Environmental health
Exome
Exome sequencing
FMR1
Feature (linguistics)
Fragile X syndrome
Fragile x
Genome
Genomics
Gestation
Image (mathematics)
Intellectual disability
Internal medicine
Linguistics
Logistic regression
Machine learning
Medical diagnosis