Niels Vos

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 6

Top Topics

Systematic Review

Dna Methylation

Top Venues

Clinical obesity

European journal of human genetics : EJHG

American journal of medical genetics. Part A

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

Publications

Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity (2024)
Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity 14 (4) (2024)
Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity 14 (4) (2024)
Niels Vos, Lotte Kleinendorst, Liselot van der Laan, Jorrit van Uhm, Philip R Jansen, Agnies M van Eeghen, Saskia M Maas, Marcel M A M Mannens, Mieke M van Haelst
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options. European journal of human genetics : EJHG (2024)
Saskia M Maas, Izabela M Krzyzewska, Maria P R Lombardi, Marcel M A Mannens, Niels Vos, Jet Bliek
Should testing for mosaic genome-wide paternal uniparental disomy in Beckwith-Wiedemann spectrum (BWSp) be implemented in diagnostic testing? European journal of human genetics : EJHG (2023)
Niels Vos, Leonie A Menke, Christiaan F Mooij, Erica L T van den Akker, Mariëlle Alders, Mieke M van Haelst
Severe early-onset overgrowth in a case of pseudohypoparathyroidism type 1b, caused by STX16 deletion. American journal of medical genetics. Part A (2023)