Fadi F. Hamdan, Ph.D.
Institution:
McGill University, Montreal, QC, CanadaArea:
Parasite NeurobiologyGoogle:
"Fadi Hamdan"Mean distance: 21.27 (cluster 32)
Parents
Sign in to add mentor| Paula A. Ribeiro | grad student | 2000 | McGill | |
| (Serotonin biosynthesis and receptors in helminths.) | ||||
| Michel Bouvier | post-doc | Université de Montréal | ||
BETA: Related publications
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Publications
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| Bell S, Rousseau J, Peng H, et al. (2019) Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. American Journal of Human Genetics |
| Alkhunaizi E, Shuster S, Shannon P, et al. (2019) Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum. American Journal of Medical Genetics. Part A |
| Manti F, Nardecchia F, Barresi S, et al. (2018) Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism. Parkinsonism & Related Disorders |
| Lessel D, Gehbauer C, Bramswig NC, et al. (2018) BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells. Brain : a Journal of Neurology |
| Accogli A, Hamdan FF, Poulin C, et al. (2018) A novel homozygous AP4B1 mutation in two brothers with AP-4 deficiency syndrome and ocular anomalies. American Journal of Medical Genetics. Part A |
| Boissel S, Fallet-Bianco C, Chitayat D, et al. (2017) Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Hamdan FF, Myers CT, Cossette P, et al. (2017) High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. American Journal of Human Genetics. 101: 664-685 |
| Meerschaut I, Rochefort D, Revençu N, et al. (2017) FOXP1-related intellectual disability syndrome: a recognisable entity. Journal of Medical Genetics |
| Rivera B, Di Iorio M, Frankum J, et al. (2017) Functionally null RAD51D missense mutation associates strongly with ovarian carcinoma. Cancer Research |
| Bramswig NC, Lüdecke HJ, Hamdan FF, et al. (2017) Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Human Genetics |