Similar articles for PMID: 31404076

Year	Number of Results
2002	1
2003	1
2004	1
2005	1
2006	3
2008	2
2009	3
2010	2
2011	6
2012	8
2013	19
2014	18
2015	12
2016	24
2017	20
2018	27
2019	31
2020	26
2021	38
2022	34
2023	12
2024	0

1

Whole genome sequencing and rare variant analysis in essential tremor families.

Odgerel Z, Sonti S, Hernandez N, Park J, Ottman R, Louis ED, Clark LN. Odgerel Z, et al. PLoS One. 2019 Aug 12;14(8):e0220512. doi: 10.1371/journal.pone.0220512. eCollection 2019. PLoS One. 2019. PMID: 31404076 Free PMC article.

2

Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.

Clark LN, Gao Y, Wang GT, Hernandez N, Ashley-Koch A, Jankovic J, Ottman R, Leal SM, Rodriguez SMB, Louis ED. Clark LN, et al. EBioMedicine. 2022 Nov;85:104290. doi: 10.1016/j.ebiom.2022.104290. Epub 2022 Sep 29. EBioMedicine. 2022. PMID: 36183486 Free PMC article.

3

Exome-wide rare variant analysis in familial essential tremor.

Diez-Fairen M, Houle G, Ortega-Cubero S, Bandres-Ciga S, Alvarez I, Carcel M, Ibañez L, Fernandez MV, Budde JP, Trotta JR, Tonda R, Chong JX, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics (UWCMG); Aguilar M, Tartari JP, Gironell A, García-Martín E, Agundez JA, Alonso-Navarro H, Jimenez-Jimenez FJ, Fernandez M, Valldeoriola F, Marti MJ, Tolosa E, Coria F, Pastor MA, Vilariño-Güell C, Rajput A, Dion PA, Cruchaga C, Rouleau GA, Pastor P. Diez-Fairen M, et al. Parkinsonism Relat Disord. 2021 Jan;82:109-116. doi: 10.1016/j.parkreldis.2020.11.021. Epub 2020 Nov 24. Parkinsonism Relat Disord. 2021. PMID: 33279834 Free PMC article.

4

Challenges in essential tremor genetics.

Clark LN, Louis ED. Clark LN, et al. Rev Neurol (Paris). 2015 Jun-Jul;171(6-7):466-74. doi: 10.1016/j.neurol.2015.02.015. Epub 2015 May 21. Rev Neurol (Paris). 2015. PMID: 26003805 Free PMC article. Review.

5

Identification of candidate genes for familial early-onset essential tremor.

Liu X, Hernandez N, Kisselev S, Floratos A, Sawle A, Ionita-Laza I, Ottman R, Louis ED, Clark LN. Liu X, et al. Eur J Hum Genet. 2016 Jul;24(7):1009-15. doi: 10.1038/ejhg.2015.228. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508575 Free PMC article.

6

Essential tremor.

Clark LN, Louis ED. Clark LN, et al. Handb Clin Neurol. 2018;147:229-239. doi: 10.1016/B978-0-444-63233-3.00015-4. Handb Clin Neurol. 2018. PMID: 29325613 Free PMC article. Review.

7

Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.

Bagnall RD, Ingles J, Dinger ME, Cowley MJ, Ross SB, Minoche AE, Lal S, Turner C, Colley A, Rajagopalan S, Berman Y, Ronan A, Fatkin D, Semsarian C. Bagnall RD, et al. J Am Coll Cardiol. 2018 Jul 24;72(4):419-429. doi: 10.1016/j.jacc.2018.04.078. J Am Coll Cardiol. 2018. PMID: 30025578 Free article.

8

Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.

Ganesh S, Ahmed P H, Nadella RK, More RP, Seshadri M, Viswanath B, Rao M, Jain S; ADBS Consortium; Mukherjee O. Ganesh S, et al. Psychiatry Clin Neurosci. 2019 Jan;73(1):11-19. doi: 10.1111/pcn.12788. Epub 2018 Dec 12. Psychiatry Clin Neurosci. 2019. PMID: 30367527 Free PMC article.

9

Genetics of essential tremor.

Jasinska-Myga B, Wider C. Jasinska-Myga B, et al. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S138-9. doi: 10.1016/S1353-8020(11)70043-8. Parkinsonism Relat Disord. 2012. PMID: 22166413 Review.

10

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing.

Srivastava A, Giangiobbe S, Kumar A, Paramasivam N, Dymerska D, Behnisch W, Witzens-Harig M, Lubinski J, Hemminki K, Försti A, Bandapalli OR. Srivastava A, et al. Front Bioeng Biotechnol. 2020 Mar 6;8:179. doi: 10.3389/fbioe.2020.00179. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32211398 Free PMC article.

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