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Journal Abstract Search
932 related items for PubMed ID: 22242659
1. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. EPICURE Consortium, Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Epilepsia; 2012 Feb; 53(2):308-18. PubMed ID: 22242659 [Abstract] [Full Text] [Related]
2. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. EPICURE ConsortiumInstitute for Medical Biometry, Informatic and Epidemiology, University of Bonn, Bonn, Germany., EMINet Consortium, Steffens M, Leu C, Ruppert AK, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel CG, Kasteleijn-Nolst Trenité D, de Haan GJ, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Steinhoff BJ, Kleefuß-Lie AA, Kunz WS, Surges R, Elger CE, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Møller RS, Hjalgrim H, Dibbens LM, Bellows S, Oliver K, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa JM, Reif PS, Rosenow F, Mörzinger M, Feucht M, Zimprich F, Kapser C, Schankin CJ, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalcin DA, Baykan B, Bebek N, Ozbek U, Gieger C, Wichmann HE, Balschun T, Ellinghaus D, Franke A, Meesters C, Becker T, Wienker TF, Hempelmann A, Schulz H, Rüschendorf F, Leber M, Pauck SM, Trucks H, Toliat MR, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Hum Mol Genet; 2012 Dec 15; 21(24):5359-72. PubMed ID: 22949513 [Abstract] [Full Text] [Related]
3. Exploration of the genetic architecture of idiopathic generalized epilepsies. Hempelmann A, Taylor KP, Heils A, Lorenz S, Prud'homme JF, Nabbout R, Dulac O, Rudolf G, Zara F, Bianchi A, Robinson R, Gardiner RM, Covanis A, Lindhout D, Stephani U, Elger CE, Weber YG, Lerche H, Nürnberg P, Kron KL, Scheffer IE, Mulley JC, Berkovic SF, Sander T. Epilepsia; 2006 Oct 15; 47(10):1682-90. PubMed ID: 17054691 [Abstract] [Full Text] [Related]
4. Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Tauer U, Lorenz S, Lenzen KP, Heils A, Muhle H, Gresch M, Neubauer BA, Waltz S, Rudolf G, Mattheisen M, Strauch K, Nürnberg P, Schmitz B, Stephani U, Sander T. Ann Neurol; 2005 Jun 15; 57(6):866-73. PubMed ID: 15929039 [Abstract] [Full Text] [Related]
5. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families. Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF. Epilepsia; 2004 May 15; 45(5):467-78. PubMed ID: 15101828 [Abstract] [Full Text] [Related]
6. A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26. Puranam RS, Jain S, Kleindienst AM, Saxena S, Kim MK, Kelly Changizi B, Padma MV, Andrews I, Elston RC, Tiwari HK, McNamara JO. Ann Neurol; 2005 Sep 15; 58(3):449-58. PubMed ID: 16130088 [Abstract] [Full Text] [Related]
7. Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13. Pinto D, Westland B, de Haan GJ, Rudolf G, da Silva BM, Hirsch E, Lindhout D, Trenité DG, Koeleman BP. Hum Mol Genet; 2005 Jan 01; 14(1):171-8. PubMed ID: 15548544 [Abstract] [Full Text] [Related]
9. The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1". Sander T, Hildmann T, Janz D, Wienker TF, Neitzel H, Bianchi A, Bauer G, Sailer U, Berek K, Schmitz B. Ann Neurol; 1995 Aug 01; 38(2):210-7. PubMed ID: 7654068 [Abstract] [Full Text] [Related]
12. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Holliday EG, McLean DE, Nyholt DR, Mowry BJ. Arch Gen Psychiatry; 2009 Oct 01; 66(10):1058-67. PubMed ID: 19805696 [Abstract] [Full Text] [Related]
15. Do idiopathic generalized epilepsies share a common susceptibility gene? Janz D, Beck-Mannagetta G, Sander T. Neurology; 1992 Apr 01; 42(4 Suppl 5):48-55. PubMed ID: 1574176 [Abstract] [Full Text] [Related]
16. Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3. Van Vlijmen-Van Keulen CJ, Rauwerda JA, Pals G. Eur J Vasc Endovasc Surg; 2005 Jul 01; 30(1):29-35. PubMed ID: 15933979 [Abstract] [Full Text] [Related]
17. Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family. Layouni S, Salzmann A, Guipponi M, Mouthon D, Chouchane L, Dogui M, Malafosse A. Epilepsy Res; 2010 Jun 01; 90(1-2):33-8. PubMed ID: 20378313 [Abstract] [Full Text] [Related]
18. Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci. Svenningsson A, Söderhäll C, Persson S, Lundberg F, Luthman H, Chung E, Gardiner M, Kockum I, Nordenskjöld A. J Hum Genet; 2012 Feb 01; 57(2):115-21. PubMed ID: 22158425 [Abstract] [Full Text] [Related]