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802 results

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Page 1
The effect of LRRK2 loss-of-function variants in humans.
Whiffin N, Armean IM, Kleinman A, Marshall JL, Minikel EV, Goodrich JK, Quaife NM, Cole JB, Wang Q, Karczewski KJ, Cummings BB, Francioli L, Laricchia K, Guan A, Alipanahi B, Morrison P, Baptista MAS, Merchant KM; Genome Aggregation Database Production Team; Genome Aggregation Database Consortium; Ware JS, Havulinna AS, Iliadou B, Lee JJ, Nadkarni GN, Whiteman C; 23andMe Research Team; Daly M, Esko T, Hultman C, Loos RJF, Milani L, Palotie A, Pato C, Pato M, Saleheen D, Sullivan PF, Alföldi J, Cannon P, MacArthur DG. Whiffin N, et al. Among authors: palotie a. Nat Med. 2020 Jun;26(6):869-877. doi: 10.1038/s41591-020-0893-5. Epub 2020 May 27. Nat Med. 2020. PMID: 32461697 Free PMC article.
Chromosome 19p13 loci in Finnish migraine with aura families.
Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M, Säkö E, Ilmavirta M, Kaprio J, Färkkilä M, Ophoff RA, Palotie A, Wessman M. Kaunisto MA, et al. Among authors: palotie a. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):85-9. doi: 10.1002/ajmg.b.30082. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15449251 Free PMC article.
The molecular genetics of migraine.
Wessman M, Kaunisto MA, Kallela M, Palotie A. Wessman M, et al. Among authors: palotie a. Ann Med. 2004;36(6):462-73. doi: 10.1080/07853890410018060. Ann Med. 2004. PMID: 15513297 Review.
Migraine: a complex genetic disorder.
Wessman M, Terwindt GM, Kaunisto MA, Palotie A, Ophoff RA. Wessman M, et al. Among authors: palotie a. Lancet Neurol. 2007 Jun;6(6):521-32. doi: 10.1016/S1474-4422(07)70126-6. Lancet Neurol. 2007. PMID: 17509487 Review.
Consistently replicating locus linked to migraine on 10q22-q23.
Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A. Anttila V, et al. Among authors: palotie a. Am J Hum Genet. 2008 May;82(5):1051-63. doi: 10.1016/j.ajhg.2008.03.003. Am J Hum Genet. 2008. PMID: 18423523 Free PMC article.
The genome-wide patterns of variation expose significant substructure in a founder population.
Jakkula E, Rehnström K, Varilo T, Pietiläinen OP, Paunio T, Pedersen NL, deFaire U, Järvelin MR, Saharinen J, Freimer N, Ripatti S, Purcell S, Collins A, Daly MJ, Palotie A, Peltonen L. Jakkula E, et al. Among authors: palotie a. Am J Hum Genet. 2008 Dec;83(6):787-94. doi: 10.1016/j.ajhg.2008.11.005. Am J Hum Genet. 2008. PMID: 19061986 Free PMC article.
Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.
McCarroll SA, Bradner JE, Turpeinen H, Volin L, Martin PJ, Chilewski SD, Antin JH, Lee SJ, Ruutu T, Storer B, Warren EH, Zhang B, Zhao LP, Ginsburg D, Soiffer RJ, Partanen J, Hansen JA, Ritz J, Palotie A, Altshuler D. McCarroll SA, et al. Among authors: palotie a. Nat Genet. 2009 Dec;41(12):1341-4. doi: 10.1038/ng.490. Nat Genet. 2009. PMID: 19935662 Free PMC article.
Distinct variants at LIN28B influence growth in height from birth to adulthood.
Widén E, Ripatti S, Cousminer DL, Surakka I, Lappalainen T, Järvelin MR, Eriksson JG, Raitakari O, Salomaa V, Sovio U, Hartikainen AL, Pouta A, McCarthy MI, Osmond C, Kajantie E, Lehtimäki T, Viikari J, Kähönen M, Tyler-Smith C, Freimer N, Hirschhorn JN, Peltonen L, Palotie A. Widén E, et al. Among authors: palotie a. Am J Hum Genet. 2010 May 14;86(5):773-82. doi: 10.1016/j.ajhg.2010.03.010. Epub 2010 Apr 15. Am J Hum Genet. 2010. PMID: 20398887 Free PMC article.
802 results