Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
- 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
Source records
- pubmed · retrieved 2026-09-26T09:21:16.143Z