Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Hiatt SM, Zhao W, Wang Z, Wan Y, Chen K, Wang K, Tan S, Barth M, Bergant G, Besnard T, Boothe E, Brunet T, Bupp C, Cogne B, Cohen JS, Coubes C, de Vries BBA, Donald M, Ellis CA, Riley Eriksson S, Ganne B, Genevieve D, Gerard B, Gonzalez Garcia A, Hendon LG, Henig N, Huss K, Isidor B, Laut T, Leadem BR, Marco EJ, Marom D, Mercimek-Andrews S, Muir AM, Navet B, Ostojić S, Peterlin B, Pfundt R, Prentice A, Prouteau C, Robinette B, Rots D, Taurina G, van Slegtenhorst M, Volozonoka L, Wessels M, West B, Zerem A, Zhang Y, Zhu B, Ziegler A, Courdier C, Fergelot P, Van Gils J, Terek S, VanNoy GE, Berlin B, Buonomo AG, McKee JL, Cooper GM, Guo H

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DOI
10.1016/j.ajhg.2026.08.013
Published
2026 Sep 4
Container
American journal of human genetics
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.ajhg.2026.08.013,
  title = {Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.},
  author = {Hiatt SM and Zhao W and Wang Z and Wan Y and Chen K and Wang K and Tan S and Barth M and Bergant G and Besnard T and Boothe E and Brunet T and Bupp C and Cogne B and Cohen JS and Coubes C and de Vries BBA and Donald M and Ellis CA and Riley Eriksson S and Ganne B and Genevieve D and Gerard B and Gonzalez Garcia A and Hendon LG and Henig N and Huss K and Isidor B and Laut T and Leadem BR and Marco EJ and Marom D and Mercimek-Andrews S and Muir AM and Navet B and Ostojić S and Peterlin B and Pfundt R and Prentice A and Prouteau C and Robinette B and Rots D and Taurina G and van Slegtenhorst M and Volozonoka L and Wessels M and West B and Zerem A and Zhang Y and Zhu B and Ziegler A and Courdier C and Fergelot P and Van Gils J and Terek S and VanNoy GE and Berlin B and Buonomo AG and McKee JL and Cooper GM and Guo H},
  year = {2026},
  journal = {American journal of human genetics},
  doi = {10.1016/j.ajhg.2026.08.013},
  url = {https://doi.org/10.1016/j.ajhg.2026.08.013}
}

RIS

TY  - JOUR
TI  - Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
AU  - Hiatt SM
AU  - Zhao W
AU  - Wang Z
AU  - Wan Y
AU  - Chen K
AU  - Wang K
AU  - Tan S
AU  - Barth M
AU  - Bergant G
AU  - Besnard T
AU  - Boothe E
AU  - Brunet T
AU  - Bupp C
AU  - Cogne B
AU  - Cohen JS
AU  - Coubes C
AU  - de Vries BBA
AU  - Donald M
AU  - Ellis CA
AU  - Riley Eriksson S
AU  - Ganne B
AU  - Genevieve D
AU  - Gerard B
AU  - Gonzalez Garcia A
AU  - Hendon LG
AU  - Henig N
AU  - Huss K
AU  - Isidor B
AU  - Laut T
AU  - Leadem BR
AU  - Marco EJ
AU  - Marom D
AU  - Mercimek-Andrews S
AU  - Muir AM
AU  - Navet B
AU  - Ostojić S
AU  - Peterlin B
AU  - Pfundt R
AU  - Prentice A
AU  - Prouteau C
AU  - Robinette B
AU  - Rots D
AU  - Taurina G
AU  - van Slegtenhorst M
AU  - Volozonoka L
AU  - Wessels M
AU  - West B
AU  - Zerem A
AU  - Zhang Y
AU  - Zhu B
AU  - Ziegler A
AU  - Courdier C
AU  - Fergelot P
AU  - Van Gils J
AU  - Terek S
AU  - VanNoy GE
AU  - Berlin B
AU  - Buonomo AG
AU  - McKee JL
AU  - Cooper GM
AU  - Guo H
PY  - 2026
JO  - American journal of human genetics
DO  - 10.1016/j.ajhg.2026.08.013
UR  - https://doi.org/10.1016/j.ajhg.2026.08.013
ER  - 

APA

SM, H., W, Z., Z, W., Y, W., K, C., K, W., S, T., M, B., G, B., T, B., E, B., T, B., C, B., B, C., JS, C., C, C., BBA, D. V., M, D., CA, E., S, R. E., B, G., D, G., B, G., A, G. G., LG, H., N, H., K, H., B, I., T, L., BR, L., EJ, M., D, M., S, M., AM, M., B, N., S, O., B, P., R, P., A, P., C, P., B, R., D, R., G, T., M, V. S., L, V., M, W., B, W., A, Z., Y, Z., B, Z., A, Z., C, C., P, F., J, V. G., S, T., GE, V., B, B., AG, B., JL, M., GM, C., & H, G. (2026). Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2026.08.013

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