Maayke A de Koning

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Venues

Journal of medical genetics

Clinical genetics

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

Publications

Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics 61 (6) (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics 61 (6) (2024)
Maayke A de Koning, Paula A Pimienta Ramirez, Monique C Haak, Xiao Han, Martina Ha Ruiterkamp-Versteeg, Nicole de Leeuw, Ulrich A Schatz, Moneef Shoukier, Esther Rieger-Fackeldey, Javier U Ortiz, Sjoerd G van Duinen, Willemijn M Klein, Ruben S G M Witlox, Richard H Finnell, Gijs W E Santen, Yunping Lei, Manon Suerink
De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of medical genetics (2024)
Maayke A de Koning, Mariëtte J V Hoffer, Esther A R Nibbeling, Emilia K Bijlsma, Menno J P Toirkens, Phebe N Adama-Scheltema, E Joanne Verweij, Marieke B Veenhof, Gijs W E Santen, Cacha M P C D Peeters-Scholte
Prenatal exome sequencing: A useful tool for the fetal neurologist. Clinical genetics 101 (1) (2021)

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Publication Activity (10 Years)

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Maayke A de Koning