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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 2 |
2011 | 1 |
2012 | 1 |
2013 | 2 |
2015 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
An immune response network associated with blood lipid levels.
PLoS Genet. 2010 Sep 9;6(9):e1001113. doi: 10.1371/journal.pgen.1001113.
PLoS Genet. 2010.
PMID: 20844574
Free PMC article.
Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.
Gaily E, Anttonen AK, Valanne L, Liukkonen E, Träskelin AL, Polvi A, Lommi M, Muona M, Eriksson K, Lehesjoki AE.
Gaily E, et al.
Epilepsia. 2013 Sep;54(9):1577-85. doi: 10.1111/epi.12256. Epub 2013 Jun 28.
Epilepsia. 2013.
PMID: 23808377
Free article.
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TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.
Sandbacka M, Laivuori H, Freitas É, Halttunen M, Jokimaa V, Morin-Papunen L, Rosenberg C, Aittomäki K.
Sandbacka M, et al.
Orphanet J Rare Dis. 2013 Aug 16;8:125. doi: 10.1186/1750-1172-8-125.
Orphanet J Rare Dis. 2013.
PMID: 23954021
Free PMC article.
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Pubertal timing and growth influences cardiometabolic risk factors in adult males and females.
Widén E, Silventoinen K, Sovio U, Ripatti S, Cousminer DL, Hartikainen AL, Laitinen J, Pouta A, Kaprio J, Järvelin MR, Peltonen L, Palotie A.
Widén E, et al.
Diabetes Care. 2012 Apr;35(4):850-6. doi: 10.2337/dc11-1365. Epub 2012 Feb 14.
Diabetes Care. 2012.
PMID: 22338106
Free PMC article.
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Phenotype mining in CNV carriers from a population cohort.
Pietiläinen OP, Rehnström K, Jakkula E, Service SK, Congdon E, Tilgmann C, Hartikainen AL, Taanila A, Heikura U, Paunio T, Ripatti S, Jarvelin MR, Isohanni M, Sabatti C, Palotie A, Freimer NB, Peltonen L.
Pietiläinen OP, et al.
Hum Mol Genet. 2011 Jul 1;20(13):2686-95. doi: 10.1093/hmg/ddr162. Epub 2011 Apr 19.
Hum Mol Genet. 2011.
PMID: 21505072
Free PMC article.
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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.
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.
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Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.
Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Tsuang MT, Glatt SJ, Chen WJ, Hwu HG; Taiwanese Trios Exome Sequencing Consortium; Neale BM, Palotie A, Sklar P, Purcell SM, McCarroll SA, Holmans P, Owen MJ, O'Donovan MC.
Rees E, et al.
Transl Psychiatry. 2015 Jul 21;5(7):e607. doi: 10.1038/tp.2015.99.
Transl Psychiatry. 2015.
PMID: 26196440
Free PMC article.
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