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论文共 74 篇作者统计合作学者相似作者

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Genomic Analyses in Cornelia De Lange Syndrome and Related Diagnoses: Novel Candidate Genes, Genotype-Phenotype Correlations and Common Mechanisms
Maninder Kaur,Justin Blair,Batsal Devkota,Sierra Fortunato,Dinah Clark, Audrey Lawrence, Jiwoo Kim, Wonwook Do, Benjamin Semeo,Olivia Katz,Devanshi Mehta,Nobuko Yamamoto,Emma Schindler, Zayd Al Rawi, Nina Wallace,Jonathan J. Wilde,Jennifer McCallum,Jinglan Liu,Dongbin Xu,Marie McDonald,Stefan Rentas,Ahmad Abou Tayoun,Zhang Zhe,Omar Abdul-Rahman, Bill Allen, Moris A. Angula,Kwame Anyane-Yeboa,Jesus Argente, Pamela H. Arn,Linlea Armstrong,Lina Basel-Salmon,Gareth Baynam,Lynne M. Bird, Daniel Bruegger,Gaik-Siew Ch'ng,David Chitayat,Robin Clark,Gerald F. Cox,Usha Dave, Elfrede DeBaere,Michael Field,John M. Graham,Karen W. Gripp,Robert Greenstein,Neerja Gupta, Randy Heidenreich,Jodi Hoffman,Robert J. Hopkin,Kenneth L. Jones,Marilyn C. Jones,Ariana Kariminejad,Jillene Kogan,Baiba Lace, Julian Leroy,Sally Ann Lynch, Kirsten Meagher,Nancy Mendelsohn,Ieva Micule,John M. Toimie,Sheela Nampoothiri, Kaoru Ohashi,Cynthia M. Powell,Subhadra Ramanathan,Salmo Raskin,Elizabeth Roeder,Marlene Rio,Alan F. Rope,Karan Sangha,Angela E. Scheuerle,Adele Schneider,Stavit Shalev,Victoria Siu,Rosemarie Smith,Cathy Stevens,Tinatin Tkemaladze,John Toimie,Helga Toriello,Anne Turner,Patricia G. Wheeler,Susan M. White,Terri Young,Kathleen M. Loomes,Mary Pipan, Ann Tokay Harrington,Elaine Zackai,Ramakrishnan Rajagopalan,Laura Conlin,Matthew A. Deardorff,Deborah McEldrew,Juan Pie,Feliciano Ramos,Antonio Musio,Antonie D. Kline,Kosuke Izumi,Sarah E. Raible,Ian D. Krantz
AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 8 (2023): 2113-2131
引用0浏览0WOS引用
0
0
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)
引用22浏览0引用
22
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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）
引用87浏览0WOS引用
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
引用5浏览0引用
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）
引用5浏览0引用
5
0
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作者统计

#Papers: 75

#Citation: 4167

H-Index: 31

G-Index: 61

Sociability: 7

Diversity: 3

Activity: 2

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