Eline A Verberne

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 11

Top Venues

Birth defects research

American journal of medical genetics. Part A

Journal of community genetics

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Eline A Verberne, Shirley M Lo-A-Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L G Wever, Eric Arends, Hilda Holtsema, Petra J Hajenius, Daphne Moreta, Ginette M Ecury-Goossen, Marcel M A M Mannens, Hermien E K de Walle, Jorieke Elisabertha Hermina Bergman, Mieke M van Haelst
Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao. Birth defects research 115 (6) (2023)
Eline A Verberne, Shirley M Lo-A-Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L G Wever, Eric Arends, Hilda Holtsema, Petra J Hajenius, Daphne Moreta, Ginette M Ecury-Goossen, Marcel M A M Mannens, Hermien E K de Walle, Jorieke Elisabertha Hermina Bergman, Mieke M van Haelst
Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao. Birth defects research (2023)
Eline A Verberne, Shirley M Lo-A-Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L G Wever, Eric Arends, Hilda Holtsema, Petra J Hajenius, Daphne Moreta, Ginette M Ecury-Goossen, Marcel M A M Mannens, Hermien E K de Walle, Jorieke Elisabertha Hermina Bergman, Mieke M van Haelst
Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao. Birth defects research 115 (6) (2023)
Eline A Verberne, Shirley M Lo-A-Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L G Wever, Eric Arends, Hilda Holtsema, Petra J Hajenius, Daphne Moreta, Ginette M Ecury-Goossen, Marcel M A M Mannens, Hermien E K de Walle, Jorieke Elisabertha Hermina Bergman, Mieke M van Haelst
Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao. Birth defects research 115 (6) (2023)
Eline A Verberne, Jonne M Westermann, Tamar I de Vries, Ginette M Ecury-Goossen, Shirley M Lo-A-Njoe, Meindert E Manshande, Sonja Faries, Hans D Veenhuis, Patricia Philippi, Farah A Falix, Irsa Rosina-Angelista, Maria Ponson-Wever, Louise Rafael-Croes, Patricia Thorsen, Eric Arends, Maartje de Vroomen, Sietse Q Nagelkerke, Martijn Tilanus, Lars T van der Veken, Karin Huijsdens-van Amsterdam, Anne-Marie van der Kevie-Kersemaekers, Mariëlle Alders, Marcel M A M Mannens, Mieke M van Haelst
Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean. American journal of medical genetics. Part A 188 (6) (2022)
Eline A Verberne, Liselot van der Laan, Sadegheh Haghshenas, Kathleen Rooney, Michael A Levy, Mariëlle Alders, Saskia M Maas, Sandra Jansen, Agne Lieden, Britt-Marie Anderlid, Louise Rafael-Croes, Philippe M Campeau, Ayeshah Chaudhry, David A Koolen, Rolph Pfundt, Anna C E Hurst, Frederic Tran-Mau-Them, Ange-Line Bruel, Laetitia Lambert, Bertrand Isidor, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman, Mieke M van Haelst
DNA Methylation Signature for JARID2 -Neurodevelopmental Syndrome. International journal of molecular sciences 23 (14) (2022)
Eline A Verberne, Ginette M Ecury-Goossen, Meindert E Manshande, Maria Ponson-Wever, Maartje de Vroomen, Martijn Tilanus, Marcel M A M Mannens, Lidewij Henneman, Mieke M van Haelst
Clinical and community genetics services in the Dutch Caribbean. Journal of community genetics 12 (3) (2021)
Eline A Verberne, Ginette M Ecury-Goossen, Meindert E Manshande, Maria Ponson-Wever, Maartje de Vroomen, Martijn Tilanus, Marcel M A M Mannens, Lidewij Henneman, Mieke M van Haelst
Clinical and community genetics services in the Dutch Caribbean. Journal of community genetics (2021)
Eline A Verberne, Shuxiang Goh, Jade England, Manon van Ginkel, Louise Rafael-Croes, Saskia Maas, Abeltje Polstra, Yuri A Zarate, Katherine A Bosanko, Kieran B Pechter, Emma Bedoukian, Kosuke Izumi, Ayeshah Chaudhry, Nathaniel H Robin, Megan Boothe, Natalie C Lippa, Vimla Aggarwal, Darryl C De Vivo, Anna Lehman, Causes Study, Sylvia Stockler, Ange-Line Bruel, Bertrand Isidor, Jennifer Lemons, David F Rodriguez-Buritica, Christopher M Richmond, Zornitza Stark, Pankaj B Agrawal, R Frank Kooy, Marije E C Meuwissen, David A Koolen, Rolf Pfundt, Agne Lieden, Britt-Marie Anderlid, Dagmar Glatz, Marcel M A M Mannens, Madhura Bakshi, Frédérick A Mallette, Mieke M van Haelst, Philippe M Campeau
JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 23 (2) (2020)
Eline A Verberne, Sonja Faries, Marcel M A M Mannens, Alex V Postma, Mieke M van Haelst
Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency. American journal of medical genetics. Part A 182 (8) (2020)
Eline A Verberne, Lotje Dalen Meurs, Nicole I Wolf, Mieke M van Haelst
4H leukodystrophy caused by a homozygous POLR3B mutation: Further delineation of the phenotype. American journal of medical genetics. Part A 182 (7) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Eline A Verberne