Similar articles for PMID: 29325607

Year	Number of Results
1999	1
2000	1
2001	4
2002	3
2003	2
2004	1
2006	1
2008	1
2009	1
2010	1
2011	5
2012	5
2013	9
2014	12
2015	17
2016	14
2017	9
2018	13
2019	11
2020	6
2021	7
2022	5
2023	6
2024	0

1

Genetic and genomic testing for neurologic disease in clinical practice.

Fogel BL. Fogel BL. Handb Clin Neurol. 2018;147:11-22. doi: 10.1016/B978-0-444-63233-3.00002-6. Handb Clin Neurol. 2018. PMID: 29325607 Review.

2

Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.

Fogel BL, Lee H, Strom SP, Deignan JL, Nelson SF. Fogel BL, et al. Ann N Y Acad Sci. 2016 Feb;1366(1):49-60. doi: 10.1111/nyas.12850. Epub 2015 Aug 6. Ann N Y Acad Sci. 2016. PMID: 26250888 Free PMC article. Review.

3

Genetic Diagnostics for Neurologists.

Silveira-Moriyama L, Paciorkowski AR. Silveira-Moriyama L, et al. Continuum (Minneap Minn). 2018 Feb;24(1, Child Neurology):18-36. doi: 10.1212/CON.0000000000000556. Continuum (Minneap Minn). 2018. PMID: 29432235 Review.

4

Genomic medicine and risk prediction across the disease spectrum.

Kotze MJ, Lückhoff HK, Peeters AV, Baatjes K, Schoeman M, van der Merwe L, Grant KA, Fisher LR, van der Merwe N, Pretorius J, van Velden DP, Myburgh EJ, Pienaar FM, van Rensburg SJ, Yako YY, September AV, Moremi KE, Cronje FJ, Tiffin N, Bouwens CS, Bezuidenhout J, Apffelstaedt JP, Hough FS, Erasmus RT, Schneider JW. Kotze MJ, et al. Crit Rev Clin Lab Sci. 2015;52(3):120-37. doi: 10.3109/10408363.2014.997930. Epub 2015 Jan 19. Crit Rev Clin Lab Sci. 2015. PMID: 25597499 Review.

5

The genetics of neuropsychiatric diseases: looking in and beyond the exome.

Heinzen EL, Neale BM, Traynelis SF, Allen AS, Goldstein DB. Heinzen EL, et al. Annu Rev Neurosci. 2015 Jul 8;38:47-68. doi: 10.1146/annurev-neuro-071714-034136. Epub 2015 Apr 2. Annu Rev Neurosci. 2015. PMID: 25840007 Review.

6

Advances in genetic diagnosis of neurological disorders.

Toft M. Toft M. Acta Neurol Scand Suppl. 2014;(198):20-5. doi: 10.1111/ane.12232. Acta Neurol Scand Suppl. 2014. PMID: 24588502 Review.

7

Diagnostic yield of next-generation sequencing applied to neurological disorders.

Marques Matos C, Alonso I, Leão M. Marques Matos C, et al. J Clin Neurosci. 2019 Sep;67:14-18. doi: 10.1016/j.jocn.2019.06.041. Epub 2019 Jul 2. J Clin Neurosci. 2019. PMID: 31272831

8

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.

Ganapathy A, Mishra A, Soni MR, Kumar P, Sadagopan M, Kanthi AV, Patric IRP, George S, Sridharan A, Thyagarajan TC, Aswathy SL, Vidya HK, Chinnappa SM, Nayanala S, Prakash MB, Raghavendrachar VG, Parulekar M, Gowda VK, Nampoothiri S, Menon RN, Pachat D, Udani V, Naik N, Kamate M, Devi ARR, Mohammed Kunju PA, Nair M, Hegde AU, Kumar MP, Sundaram S, Tilak P, Puri RD, Shah K, Sheth J, Hasan Q, Sheth F, Agrawal P, Katragadda S, Veeramachaneni V, Chandru V, Hariharan R, Mannan AU. Ganapathy A, et al. J Neurol. 2019 Aug;266(8):1919-1926. doi: 10.1007/s00415-019-09358-1. Epub 2019 May 8. J Neurol. 2019. PMID: 31069529

9

Clinical pertinence metric enables hypothesis-independent genome-phenome analysis for neurologic diagnosis.

Segal MM, Abdellateef M, El-Hattab AW, Hilbush BS, De La Vega FM, Tromp G, Williams MS, Betensky RA, Gleeson J. Segal MM, et al. J Child Neurol. 2015 Jun;30(7):881-8. doi: 10.1177/0883073814545884. Epub 2014 Aug 24. J Child Neurol. 2015. PMID: 25156663 Free PMC article.

10

Genome sequencing and implications for rare disorders.

Posey JE. Posey JE. Orphanet J Rare Dis. 2019 Jun 24;14(1):153. doi: 10.1186/s13023-019-1127-0. Orphanet J Rare Dis. 2019. PMID: 31234920 Free PMC article. Review.

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