KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

Awamleh Z, Chen A, Choufani S, Rots D, Ko JM, Armour CM, Nowaczyk MJM, Hurst ACE, Gibson WT, Misceo D, Frengen E, Strømme P, Soliani L, McNiven V, Alkhunaizi E, Invernizzi F, Fernandes S, Sousa S, Amoros I, Scherer SW, Kwint M, Bienvenu T, Garavaglia BM, Ortigoza-Escobar JD, Weksberg R

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DOI: 10.1016/j.gim.2026.102636
Published: 2026 Jun 19
Container: Genetics in medicine : official journal of the American College of Medical Genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1016/j.gim.2026.102636,
  title = {KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.},
  author = {Awamleh Z and Chen A and Choufani S and Rots D and Ko JM and Armour CM and Nowaczyk MJM and Hurst ACE and Gibson WT and Misceo D and Frengen E and Strømme P and Soliani L and McNiven V and Alkhunaizi E and Invernizzi F and Fernandes S and Sousa S and Amoros I and Scherer SW and Kwint M and Bienvenu T and Garavaglia BM and Ortigoza-Escobar JD and Weksberg R},
  year = {2026},
  journal = {Genetics in medicine : official journal of the American College of Medical Genetics},
  doi = {10.1016/j.gim.2026.102636},
  url = {https://doi.org/10.1016/j.gim.2026.102636}
}

RIS

TY  - JOUR
TI  - KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.
AU  - Awamleh Z
AU  - Chen A
AU  - Choufani S
AU  - Rots D
AU  - Ko JM
AU  - Armour CM
AU  - Nowaczyk MJM
AU  - Hurst ACE
AU  - Gibson WT
AU  - Misceo D
AU  - Frengen E
AU  - Strømme P
AU  - Soliani L
AU  - McNiven V
AU  - Alkhunaizi E
AU  - Invernizzi F
AU  - Fernandes S
AU  - Sousa S
AU  - Amoros I
AU  - Scherer SW
AU  - Kwint M
AU  - Bienvenu T
AU  - Garavaglia BM
AU  - Ortigoza-Escobar JD
AU  - Weksberg R
PY  - 2026
JO  - Genetics in medicine : official journal of the American College of Medical Genetics
DO  - 10.1016/j.gim.2026.102636
UR  - https://doi.org/10.1016/j.gim.2026.102636
ER  -

APA

Z, A., A, C., S, C., D, R., JM, K., CM, A., MJM, N., ACE, H., WT, G., D, M., E, F., P, S., L, S., V, M., E, A., F, I., S, F., S, S., I, A., SW, S., M, K., T, B., BM, G., JD, O., & R, W. (2026). KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.. Genetics in medicine : official journal of the American College of Medical Genetics. https://doi.org/10.1016/j.gim.2026.102636

Source records

pubmed · retrieved 2026-09-26T21:47:48.720Z