De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.

Bradbrook SM, Graham G, Carter MT, Kibaek M, Fagerberg C, Larsen MJ, Dawson K, Meuter C, Pepler A, Besnard T, Vincent M, Isidor B, Bezieau S, Cogne B, Bjørgo K, Amundsen SS, Courtin T, Emrick L, Rosenfeld JA, Weisz-Hubshman M, Undiagnosed Diseases Network, Mak BC, Martinez-Agosto J, Heulin M, Morin G, Keren B, Schutz S, Monin P, Pujalte M, Januel L, Lesca G, Valence MB, Margot H, Levy J, Iovino E, Isidori F, Pippucci T, Montanari F, Bell L, Burton J, Torti E, Wentzensen IM, Marcadier J

Open source

DOI
10.1002/ajmg.a.64242
Published
2026 Jan
Container
American journal of medical genetics. Part A
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1002/ajmg.a.64242,
  title = {De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.},
  author = {Bradbrook SM and Graham G and Carter MT and Kibaek M and Fagerberg C and Larsen MJ and Dawson K and Meuter C and Pepler A and Besnard T and Vincent M and Isidor B and Bezieau S and Cogne B and Bjørgo K and Amundsen SS and Courtin T and Emrick L and Rosenfeld JA and Weisz-Hubshman M and Undiagnosed Diseases Network and Mak BC and Martinez-Agosto J and Heulin M and Morin G and Keren B and Schutz S and Monin P and Pujalte M and Januel L and Lesca G and Valence MB and Margot H and Levy J and Iovino E and Isidori F and Pippucci T and Montanari F and Bell L and Burton J and Torti E and Wentzensen IM and Marcadier J},
  year = {2026},
  journal = {American journal of medical genetics. Part A},
  doi = {10.1002/ajmg.a.64242},
  url = {https://doi.org/10.1002/ajmg.a.64242}
}

RIS

TY  - JOUR
TI  - De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.
AU  - Bradbrook SM
AU  - Graham G
AU  - Carter MT
AU  - Kibaek M
AU  - Fagerberg C
AU  - Larsen MJ
AU  - Dawson K
AU  - Meuter C
AU  - Pepler A
AU  - Besnard T
AU  - Vincent M
AU  - Isidor B
AU  - Bezieau S
AU  - Cogne B
AU  - Bjørgo K
AU  - Amundsen SS
AU  - Courtin T
AU  - Emrick L
AU  - Rosenfeld JA
AU  - Weisz-Hubshman M
AU  - Undiagnosed Diseases Network
AU  - Mak BC
AU  - Martinez-Agosto J
AU  - Heulin M
AU  - Morin G
AU  - Keren B
AU  - Schutz S
AU  - Monin P
AU  - Pujalte M
AU  - Januel L
AU  - Lesca G
AU  - Valence MB
AU  - Margot H
AU  - Levy J
AU  - Iovino E
AU  - Isidori F
AU  - Pippucci T
AU  - Montanari F
AU  - Bell L
AU  - Burton J
AU  - Torti E
AU  - Wentzensen IM
AU  - Marcadier J
PY  - 2026
JO  - American journal of medical genetics. Part A
DO  - 10.1002/ajmg.a.64242
UR  - https://doi.org/10.1002/ajmg.a.64242
ER  - 

APA

SM, B., G, G., MT, C., M, K., C, F., MJ, L., K, D., C, M., A, P., T, B., M, V., B, I., S, B., B, C., K, B., SS, A., T, C., L, E., JA, R., M, W., Network, U. D., BC, M., J, M., M, H., G, M., B, K., S, S., P, M., M, P., L, J., G, L., MB, V., H, M., J, L., E, I., F, I., T, P., F, M., L, B., J, B., E, T., IM, W., & J, M. (2026). De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.. American journal of medical genetics. Part A. https://doi.org/10.1002/ajmg.a.64242

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