Najm IM - Search Results

Year	Number of Results
1996	1
1997	1
1998	2
1999	1
2000	2
2001	1
2002	4
2003	1
2004	4
2005	3
2006	3
2007	6
2008	4
2009	6
2010	1
2011	3
2012	9
2013	9
2014	5
2015	1
2016	6
2017	7
2018	9
2019	6
2020	5
2021	3
2022	6
2023	3
2024	4

1

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.

International League Against Epilepsy Consortium on Complex Epilepsies. International League Against Epilepsy Consortium on Complex Epilepsies. Nat Genet. 2023 Sep;55(9):1471-1482. doi: 10.1038/s41588-023-01485-w. Epub 2023 Aug 31. Nat Genet. 2023. PMID: 37653029 Free PMC article.

2

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Montanucci L, Lewis-Smith D, Collins RL, Niestroj LM, Parthasarathy S, Xian J, Ganesan S, Macnee M, Brünger T, Thomas RH, Talkowski M; Epi25 Collaborative; Helbig I, Leu C, Lal D. Montanucci L, et al. Nat Commun. 2023 Jul 20;14(1):4392. doi: 10.1038/s41467-023-39539-6. Nat Commun. 2023. PMID: 37474567 Free PMC article.

3

MR imaging in epilepsy.

Ruggieri PM, Najm IM. Ruggieri PM, et al. Among authors: najm im. Neurol Clin. 2001 May;19(2):477-89. doi: 10.1016/s0733-8619(05)70027-x. Neurol Clin. 2001. PMID: 11358753 Review.

4

Epilepsies associated with focal cortical dysplasias (FCDs).

Najm IM, Tassi L, Sarnat HB, Holthausen H, Russo GL. Najm IM, et al. Acta Neuropathol. 2014 Jul;128(1):5-19. doi: 10.1007/s00401-014-1304-0. Epub 2014 Jun 12. Acta Neuropathol. 2014. PMID: 24916270 Review.

5

Polygenic burden in focal and generalized epilepsies.

Leu C, Stevelink R, Smith AW, Goleva SB, Kanai M, Ferguson L, Campbell C, Kamatani Y, Okada Y, Sisodiya SM, Cavalleri GL, Koeleman BPC, Lerche H, Jehi L, Davis LK, Najm IM, Palotie A, Daly MJ, Busch RM; Epi25 Consortium; Lal D. Leu C, et al. Among authors: najm im. Brain. 2019 Nov 1;142(11):3473-3481. doi: 10.1093/brain/awz292. Brain. 2019. PMID: 31608925 Free PMC article.

6

Polygenic risk heterogeneity among focal epilepsies.

Gramm M, Leu C, Pérez-Palma E, Ferguson L, Jehi L, Daly MJ, Najm IM, Busch RM, Lal D. Gramm M, et al. Among authors: najm im. Epilepsia. 2020 Nov;61(11):e179-e185. doi: 10.1111/epi.16717. Epub 2020 Oct 14. Epilepsia. 2020. PMID: 33090489

7

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Epi25 Collaborative. Epi25 Collaborative. Nat Neurosci. 2024 Oct;27(10):1864-1879. doi: 10.1038/s41593-024-01747-8. Epub 2024 Oct 3. Nat Neurosci. 2024. PMID: 39363051

8

Review: The international consensus classification of Focal Cortical Dysplasia - a critical update 2018.

Najm IM, Sarnat HB, Blümcke I. Najm IM, et al. Neuropathol Appl Neurobiol. 2018 Feb;44(1):18-31. doi: 10.1111/nan.12462. Neuropathol Appl Neurobiol. 2018. PMID: 29359399 Review.

9

Magnetic resonance spectroscopy in animal models of epilepsy.

Hiremath GK, Najm IM. Hiremath GK, et al. Among authors: najm im. Epilepsia. 2007;48 Suppl 4:47-55. doi: 10.1111/j.1528-1167.2007.01241.x. Epilepsia. 2007. PMID: 17767575 Free article. Review.

10

Indications and selection criteria for invasive monitoring in children with cortical dysplasia.

Gonzalez-Martinez J, Najm IM. Gonzalez-Martinez J, et al. Among authors: najm im. Childs Nerv Syst. 2014 Nov;30(11):1823-9. doi: 10.1007/s00381-014-2497-1. Epub 2014 Oct 9. Childs Nerv Syst. 2014. PMID: 25296543 Review.

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