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Research Interests

Papers共 32 篇Author StatisticsCo-AuthorSimilar Experts

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DDX3X-related Neurodevelopmental Disorder in Males - Presenting a New Cohort of 19 Males and a Literature Review
Milou G P Kennis,Dmitrijs Rots,Arjan Bouman,Charlotte W Ockeloen, Caroline Boelen, Carlo L M Marcelis,Bert B A de Vries,Mariet W Elting,Quinten Waisfisz,Mohnish Suri, Esperanza Font-Montgomery, Dawn S Peck, Deirdre E Donnelly,R Curtis Rogers, Ruth Richardson,Roseline Caumes,Boris Chaumette, Cécile Louveau,Suzanne C E H Sallevelt,Saskia M Maas, Jeroen J Smits, Mieke M van Haelst, Rebecca J Levy,Helen Stewart, Bart L Loeys,Rolph Pfundt,Tjitske Kleefstra, Lot Snijders Blok
European journal of human genetics EJHG（2025）
Cited0Views0WOSNATUREBibtex
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Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2018), 10.1038/s41436-018-0330-z)
Pleuntje J. van der Sluijs,Sandra Jansen,Samantha A. Vergano,Miho Adachi-Fukuda,Yasemin Alanay,Adila AlKindy,Anwar Baban,Allan Bayat,Stefanie Beck-Wödl,Katherine Berry,Emilia K. Bijlsma,Levinus A. Bok,Alwin F. J. Brouwer,Ineke van der Burgt,Philippe M. Campeau,Natalie Canham,Krystyna Chrzanowska,Yoyo W. Y. Chu,Brain H. Y. Chung,Karin Dahan,Marjan de Rademaeker,Anne Destree,Tracy Dudding-Byth,Rachel Earl,Nursel Elcioglu,Ellen R. Elias,Christina Fagerberg,Alice Gardham,Blanca Gener,Erica H. Gerkes,Ute Grasshoff,Arie van Haeringen,Karin R. Heitink,Johanna C. Herkert,Nicolette S. den Hollander,Denise Horn,David Hunt,Sarina G. Kant,Mitsuhiro Kato,H. lya Kayserili,Rogier Kersseboom,Esra Kilic,Malgorzata Krajewska-Walasek,Kylin Lammers,Lone W. Laulund,Damien Lederer,Melissa Lees,Vanesa López-González,Saskia Maas,Grazia M. S. Mancini,Carlo Marcelis,Francisco Martinez,Isabelle Maystadt,Marianne McGuire,Shane McKee,Sarju Mehta,Kay Metcalfe,Jeff Milunsky,Seiji Mizuno,John B. Moeschler,Christian Netzer,Charlotte W. Ockeloen,Barbara Oehl-Jaschkowitz,Nobuhiko Okamoto,Sharon N. M. Olminkhof,Carmen Orellana,Laurent Pasquier,Caroline Pottinger,Vera Riehmer,Stephen P. Robertson,Maian Roifman,Caroline Rooryck,Fabienne G. Ropers,Monica Rosello,Claudia A. L. Ruivenkamp,Mahmut S. Sagiroglu,Suzanne C. E. H. Sallevelt,Amparo Sanchis Calvo,Pelin O. Simsek-Kiper,Gabriela Soares,Lucia Solaeche,Fatma Mujgan Sonmez,Miranda Splitt,Duco Steenbeek,Alexander P. A. Stegmann,Constance T. R. M. Stumpel,Saori Tanabe,Eyyup Uctepe,G. Eda Utine,Hermine E. Veenstra-Knol,Sunita Venkateswaran,Catheline Vilain,Catherine Vincent-Delorme,Anneke T. Vulto-van Silfhout,Patricia Wheeler,Golder N. Wilson,Louise C. Wilson,Bernd Wollnik,Tomoki Kosho,Dagmar Wieczorek,Evan Eichler,Rolph Pfundt,Bert B. A. de Vries,Jill Clayton-Smith,Gijs W. E. Santen
Genetics in Medicine (2019)
Cited22Views0Bibtex
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Author Statistics

#Papers: 32

#Citation: 1077

H-Index: 16

G-Index: 27

Sociability: 6

Diversity: 2

Activity: 6

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