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Papers共 86 篇Author StatisticsCo-AuthorSimilar Experts

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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
22
0
The ARID1B Spectrum in 143 Patients: from Nonsyndromic Intellectual Disability to Coffin–Siris Syndrome
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,Hülya 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）
Cited87Views0WOSBibtex
87
0
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)
Pleuntje J. van der Sluijs,Sandra Jansen,Samantha A. Vergano,Miho Adachi-Fukuda,Yasemin Alanay,Adila Al-Kindy,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 H. Chrzanowska,Yoyo W. Y. Chu,Brain H. Y. Chung,Karin Dahan,Marjan De Rademaeker,Anne Destree,Tracy Dudding-Byth,Rachel K. 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 Kılıç,Małgorzata Krajewska-Walasek,Kylin Lammers,Lone W. Laulund,Damien Lederer,Melissa Lees,Vanesa López-González,Saskia M. Maas,Grazia M.S. Mancini,Carlo Marcelis,Francisco Martínez,Isabelle Maystadt,Marianne McGuire,Shane McKee,Sarju G. Mehta,Kay Metcalfe,Jeff M. 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,Mónica Roselló,Claudia A. L. Ruivenkamp,Mahmut Şamil Sağıroğlu,Suzanne C E H Sallevelt,Amparo Sanchis Calvo,Pelin Ozlem 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 G. Wheeler,Golder N. Wilson,Louise C. Wilson,Bernd Wollnik,Tomoki Kosho,Dagmar Wieczorek
Genetics in Medicineno. 9 (2019): 2160-2161
Cited5Views0Bibtex
5
0
The Arid1b Spectrum In 143 Patients: From Nonsyndromic Intellectual Disability To Coffin-Siris Syndrome (Vol 21, Pg 1295, 2019)
Pleuntje J. Van Der Sluijs,Sandra Jansen,Samantha A. Vergano,Miho Adachi-Fukuda,Yasemin Alanay,Adila Alkindy,Anwar Baban,Allan Bayat,Stefanie Beck-Woedl,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,Hulya Kayserili,Rogier Kersseboom,Esra Kilic,Malgorzata Krajewska-Walasek,Kylin Lammers,Lone W. Laulund,Damien Lederer,Melissa Lees,Vanesa Lopez-Gonzalez,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）
Cited5Views0Bibtex
5
0
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#Papers: 86

#Citation: 8303

H-Index: 37

G-Index: 86

Sociability: 7

Diversity: 0

Activity: 0

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