Human Genome Epidemiology Literature Finder
|
Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and FOXP2[original query] |
|---|
| Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatric genetics 2008 Dec 18 (6): 295-301. Laroche Fabrice, Ramoz Nicolas, Leroy Sophie, Fortin Célia, Rousselot-Paillet Bérangère, Philippe Anne, Colleaux Laurence, Bresson Jean-Louis, Mogenet Agnès, Golse Bernard, Mouren-Simeoni Marie-Christine, Gorwood Philip, Galli Thierry, Simonneau Michel, Krebs Marie-Odile, Robel Lauren |
| The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration. Journal of Alzheimer's disease : JAD 2010 22 (3): 923-31. Padovani Alessandro, Cosseddu Maura, Premi Enrico, Archetti Silvana, Papetti Alice, Agosti Chiara, Bigni Barbara, Cerini Carlo, Paghera Barbara, Bellelli Giuseppe, Borroni Barba |
| FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies. BMC medical genetics 2010 11 (1): 114. Tolosa Amparo, Sanjuán Julio, Dagnall Adam M, Moltó María D, Herrero Neus, de Frutos Ro |
| Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients. Neuroscience letters 2011 Apr 493 (3): 131-5. Španiel Filip, Horá?ek Ji?í, Tint?ra Jaroslav, Ibrahim Ibrahim, Novák Tomáš, ?ermák Jan, Klírová Monika, Höschl Cyr |
| FOXP2, APOE, and PRNP: new modulators in primary progressive aphasia. Journal of Alzheimer's disease : JAD 2012 28 (4): 941-50. Premi Enrico, Pilotto Andrea, Alberici Antonella, Papetti Alice, Archetti Silvana, Seripa Davide, Daniele Antonio, Masullo Carlo, Garibotto Valentina, Paghera Barbara, Caobelli Federico, Padovani Alessandro, Borroni Barba |
A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Gut 2012 Aug . Julià A, Domènech E, Ricart E, Tortosa R, García-Sánchez V, Pérez Gisbert J, Nos Mateu P, Gutiérrez A, Gomollón F, Mendoza JL, Garcia-Planella E, Barreiro-de Acosta M, Muñoz F, Vera M, Saro C, Esteve M, Andreu M, Alonso A, López-Lasanta M, Codó L, Gelpí JL, García-Montero AC, Bertanpetit J, Absher D, Panés J, Marsal S |
| Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. PloS one 2013 8 (3): e58048. Walters Robin G, Coin Lachlan J M, Ruokonen Aimo, de Smith Adam J, El-Sayed Moustafa Julia S, Jacquemont Sebastien, Elliott Paul, Esko Tõnu, Hartikainen Anna-Liisa, Laitinen Jaana, Männik Katrin, Martinet Danielle, Meyre David, Nauck Matthias, Schurmann Claudia, Sladek Rob, Thorleifsson Gudmar, Thorsteinsdóttir Unnur, Valsesia Armand, Waeber Gerard, Zufferey Flore, Balkau Beverley, Pattou François, Metspalu Andres, Völzke Henry, Vollenweider Peter, Stefansson Kári, Järvelin Marjo-Riitta, Beckmann Jacques S, Froguel Philippe, Blakemore Alexandra I |
| Etiological yield of SNP microarrays in idiopathic intellectual disability. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2014 May 18 (3): 327-37. Utine G Eda, Halilo?lu Göknur, Volkan-Salanc? Bilge, Çetinkaya Arda, Kiper Pelin Ö, Alanay Yasemin, Akta? Dilek, Anlar Banu, Topçu Meral, Boduro?lu Koray, Alika?ifo?lu Mehm |
| Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
| Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Translational psychiatry 2019 02 9 (1): 14. Arnau-Soler Aleix, Macdonald-Dunlop Erin, Adams Mark J, Clarke Toni-Kim, MacIntyre Donald J, Milburn Keith, Navrady Lauren, , , Hayward Caroline, McIntosh Andrew M, Thomson Pippa |
| FOXP2 expression and gray matter density in the male brains of patients with schizophrenia. Brain imaging and behavior 2020 Jul . Sanjuán Julio, Castro-Martínez Xochitl Helga, García-Martí Gracián, González-Fernández Javier, Sanz-Requena Roberto, Haro Josep María, Meana J Javier, Martí-Bonmatí Luis, Nacher Juan, Sebastiá-Ortega Noelia, Gilabert-Juan Javier, Moltó María Dolor |
| A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
| Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes. Noro psikiyatri arsivi 2021 9 58 (3): 171-175. Yalçintepe Sinem, Görker I??k, Demir Selma, Atli Emine ?kbal, Atli Engin, Tozkir Hilmi, Süt Necdet, Özen Yasemin, Eker Damla, Mail Çisem, Güler Hazal Sezginer, Zhuri Drenushe, Gurkan Hak |
| Predicted regulatory SNPs reveal potential drug targets and novel companion diagnostics in psoriasis. Journal of translational autoimmunity 2021 4 100096. Ruiz Ramírez Andrea Virginia, Flores-Saiffe Farías Adolfo, Chávez Álvarez Rocío Del Carmen, Prado Montes de Oca Ernes |
| Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population. Heliyon 2024 6 10 (11): e31624. Paolina Crocco, Francesco De Rango, Francesco Bruno, Antonio Malvaso, Raffaele Maletta, Amalia C Bruni, Giuseppe Passarino, Giuseppina Rose, Serena Da |
- Page last reviewed:Feb 1, 2024
- Content source: