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Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor

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How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor

E. Louis, J. Ferreira. (2010). Movement Disorders. Cited 831 times. https://doi.org/10.1002/mds.22838

Exome sequencing identifies FUS mutations as a cause of essential tremor.

Nancy D. Merner, S. Girard, H. Catoire, et al. (2012). American journal of human genetics. Cited 186 times. https://doi.org/10.1016/j.ajhg.2012.07.002

Risk of tremor and impairment from tremor in relatives of patients with essential tremor: A community‐based family study

E. Louis, B. Ford, S. Frucht, et al. (2001). Annals of Neurology. Cited 178 times. https://doi.org/10.1002/ana.1022

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

A. Shatunov, N. Sambuughin, J. Jankovic, et al. (2006). Brain : a journal of neurology. Cited 137 times. https://doi.org/10.1093/BRAIN/AWL120

Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor

Sandra Thier, D. Lorenz, M. Nothnagel, et al. (2012). Neurology. Cited 115 times. https://doi.org/10.1212/WNL.0b013e31825fdeed

Replication of the LINGO1 gene association with essential tremor in a North American population

L. Clark, N. Park, S. Kisselev, et al. (2010). European Journal of Human Genetics. Cited 73 times. https://doi.org/10.1038/ejhg.2010.27

Genetic heterogeneity in autosomal dominant essential tremor

M. J. Kovach, Jimmy Ruiz, Katerina Kimonis, et al. (2001). Genetics in Medicine. Cited 67 times. https://doi.org/10.1097/00125817-200105000-00009

Application of medical genetics in Turkey.

E. Tunçbilek, M. Ozgüç. (2007). The Turkish journal of pediatrics. Cited 47 times.

Prevalence of essential tremor: a door-to-door survey in Sile, Istanbul, Turkey.

H. Sur, Selen Ilhan, H. Erdoğan, et al. (2009). Parkinsonism & related disorders. Cited 39 times. https://doi.org/10.1016/j.parkreldis.2008.03.009

Identification of candidate genes for familial early-onset essential tremor

Xinmin Liu, N. Hernandez, S. Kisselev, et al. (2015). European Journal of Human Genetics. Cited 37 times. https://doi.org/10.1038/ejhg.2015.228

Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey

A. Sazcı, E. Ergul, K. Bayulkem. (2004). Movement Disorders. Cited 33 times. https://doi.org/10.1002/mds.20254

Gamma-aminobutyric acid (GABA) receptor rho (GABRR) polymorphisms and risk for essential tremor

E. García-Martín, C. Martı́nez, H. Alonso-Navarro, et al. (2011). Journal of Neurology. Cited 31 times. https://doi.org/10.1007/s00415-010-5708-z

Challenges in essential tremor genetics.

L. Clark, E. Louis. (2015). Revue neurologique. Cited 29 times. https://doi.org/10.1016/j.neurol.2015.02.015

Investigation of the prevalence of essential tremor in individuals aged 18–60 in Erzurum

Lütfi Özel, Recep Demir, G. Özdemir, et al. (2013). Acta Neurologica Belgica. Cited 12 times. https://doi.org/10.1007/s13760-012-0147-5

The microtubule associated protein tau H1 haplotype and risk of essential tremor

L. Clark, X. Liu, N. Parmalee, et al. (2014). European Journal of Neurology. Cited 11 times. https://doi.org/10.1111/ene.12335