| Year |
Citation |
Score |
| 2024 |
Heim F, Scharff C, Fisher SE, Riebel K, Ten Cate C. Auditory discrimination learning and acoustic cue weighing in female zebra finches with localised FoxP1 knockdowns. Journal of Neurophysiology. PMID 38629163 DOI: 10.1152/jn.00228.2023 |
0.753 |
|
| 2024 |
de Hoyos L, Barendse MT, Schlag F, van Donkelaar MMJ, Verhoef E, Shapland CY, Klassmann A, Buitelaar J, Verhulst B, Fisher SE, Rai D, St Pourcain B. Structural models of genome-wide covariance identify multiple common dimensions in autism. Nature Communications. 15: 1770. PMID 38413609 DOI: 10.1038/s41467-024-46128-8 |
0.335 |
|
| 2023 |
Alagöz G, Eising E, Mekki Y, Bignardi G, Fontanillas P, Nivard MG, Luciano M, Cox NJ, Fisher SE, Gordon RL. The shared genetic architecture and evolution of human language and musical rhythm. Biorxiv : the Preprint Server For Biology. PMID 37961248 DOI: 10.1101/2023.11.01.564908 |
0.321 |
|
| 2023 |
Heim F, Fisher SE, Scharff C, Ten Cate C, Riebel K. Effects of cortical FoxP1 knockdowns on learned song preference in female zebra finches. Eneuro. PMID 36931727 DOI: 10.1523/ENEURO.0328-22.2023 |
0.747 |
|
| 2023 |
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, ... ... Fisher SE, et al. Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics. PMID 36823321 DOI: 10.1038/s41588-023-01336-8 |
0.663 |
|
| 2023 |
Abbondanza F, Dale PS, Wang CA, Hayiou-Thomas ME, Toseeb U, Koomar TS, Wigg KG, Feng Y, Price KM, Kerr EN, Guger SL, Lovett MW, Strug LJ, van Bergen E, Dolan CV, ... ... Fisher SE, et al. Language and reading impairments are associated with increased prevalence of non-right-handedness. Child Development. PMID 36780127 DOI: 10.1111/cdev.13914 |
0.678 |
|
| 2023 |
Kaspi A, Hildebrand MS, Jackson VE, Braden R, van Reyk O, Howell T, Debono S, Lauretta M, Morison L, Coleman MJ, Webster R, Coman D, Goel H, Wallis M, Dabscheck G, ... ... Fisher SE, et al. Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular Psychiatry. PMID 36658335 DOI: 10.1038/s41380-022-01879-y |
0.311 |
|
| 2022 |
Nayak S, Coleman PL, Ladányi E, Nitin R, Gustavson DE, Fisher SE, Magne CL, Gordon RL. The Musical Abilities, Pleiotropy, Language, and Environment (MAPLE) Framework for Understanding Musicality-Language Links Across the Lifespan. Neurobiology of Language (Cambridge, Mass.). 3: 615-664. PMID 36742012 DOI: 10.1162/nol_a_00079 |
0.37 |
|
| 2022 |
Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL, Fisher SE, Lovett MW, Strug LJ, Barr CL. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry. 12: 495. PMID 36446759 DOI: 10.1038/s41398-022-02250-z |
0.363 |
|
| 2022 |
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, ... ... Fisher SE, et al. Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics. PMID 36266505 DOI: 10.1038/s41588-022-01192-y |
0.724 |
|
| 2022 |
Alagöz G, Molz B, Eising E, Schijven D, Francks C, Stein JL, Fisher SE. Using neuroimaging genomics to investigate the evolution of human brain structure. Proceedings of the National Academy of Sciences of the United States of America. 119: e2200638119. PMID 36161899 DOI: 10.1073/pnas.2200638119 |
0.34 |
|
| 2022 |
Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, ... ... Fisher SE, et al. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America. 119: e2202764119. PMID 35998220 DOI: 10.1073/pnas.2202764119 |
0.744 |
|
| 2022 |
Chormai P, Pu Y, Hu H, Fisher SE, Francks C, Kong XZ. Machine learning of large-scale multimodal brain imaging data reveals neural correlates of hand preference. Neuroimage. 262: 119534. PMID 35931311 DOI: 10.1016/j.neuroimage.2022.119534 |
0.449 |
|
| 2021 |
Park BY, Larivière S, Rodríguez-Cruces R, Royer J, Tavakol S, Wang Y, Caciagli L, Caligiuri ME, Gambardella A, Concha L, Keller SS, Cendes F, Alvim MKM, Yasuda C, Bonilha L, ... ... Fisher SE, et al. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy. Brain : a Journal of Neurology. PMID 35333312 DOI: 10.1093/brain/awab417 |
0.377 |
|
| 2021 |
Shapland CY, Verhoef E, Davey Smith G, Fisher SE, Verhulst B, Dale PS, St Pourcain B. Multivariate genome-wide covariance analyses of literacy, language and working memory skills reveal distinct etiologies. Npj Science of Learning. 6: 23. PMID 34413317 DOI: 10.1038/s41539-021-00101-y |
0.312 |
|
| 2021 |
Blok LS, Goosen YM, van Haaften L, van Hulst K, Fisher SE, Brunner HG, Egger JIM, Kleefstra T. Speech-language profiles in the context of cognitive and adaptive functioning in SATB2-associated syndrome. Genes, Brain, and Behavior. e12761. PMID 34241948 DOI: 10.1111/gbb.12761 |
0.328 |
|
| 2021 |
Braden RO, Amor DJ, Fisher SE, Mei C, Myers CT, Mefford H, Gill D, Srivastava S, Swanson LC, Goel H, Scheffer IE, Morgan AT. Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Developmental Medicine and Child Neurology. PMID 34109629 DOI: 10.1111/dmcn.14955 |
0.336 |
|
| 2021 |
Carrion-Castillo A, Estruch SB, Maassen B, Franke B, Francks C, Fisher SE. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Human Genetics. PMID 34076780 DOI: 10.1007/s00439-021-02289-w |
0.351 |
|
| 2021 |
Morgan A, Braden R, Wong MMK, Colin E, Amor D, Liégeois F, Srivastava S, Vogel A, Bizaoui V, Ranguin K, Fisher SE, van Bon BW. Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics : Ejhg. PMID 33907317 DOI: 10.1038/s41431-021-00894-x |
0.361 |
|
| 2021 |
Kong XZ, Postema M, Schijven D, Castillo AC, Pepe A, Crivello F, Joliot M, Mazoyer B, Fisher SE, Francks C. Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew. Cerebral Cortex (New York, N.Y. : 1991). PMID 33836062 DOI: 10.1093/cercor/bhab075 |
0.461 |
|
| 2021 |
Guadalupe T, Kong XZ, Akkermans SEA, Fisher SE, Francks C. Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults. Brain Structure & Function. PMID 33502621 DOI: 10.1007/s00429-021-02220-z |
0.45 |
|
| 2020 |
Kong XZ, Tzourio-Mazoyer N, Joliot M, Fedorenko E, Liu J, Fisher SE, Francks C. Gene Expression Correlates of the Cortical Network Underlying Sentence Processing. Neurobiology of Language (Cambridge, Mass.). 1: 77-103. PMID 36794006 DOI: 10.1162/nol_a_00004 |
0.518 |
|
| 2020 |
Urbanus BHA, Peter S, Fisher SE, De Zeeuw CI. Region-specific Foxp2 deletions in cortex, striatum or cerebellum cannot explain vocalization deficits observed in spontaneous global knockouts. Scientific Reports. 10: 21631. PMID 33303861 DOI: 10.1038/s41598-020-78531-8 |
0.309 |
|
| 2020 |
Tilot AK, Khramtsova EA, Liang D, Grasby KL, Jahanshad N, Painter J, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Liu S, Brotman SM, Thompson PM, Medland SE, Macciardi F, ... ... Fisher SE, et al. The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area. Cerebral Cortex (New York, N.Y. : 1991). PMID 33290510 DOI: 10.1093/cercor/bhaa327 |
0.302 |
|
| 2020 |
Snijders Blok L, Vino A, den Hoed J, Underhill HR, Monteil D, Li H, Reynoso Santos FJ, Chung WK, Amaral MD, Schnur RE, Santiago-Sim T, Si Y, Brunner HG, Kleefstra T, Fisher SE. Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33110267 DOI: 10.1038/s41436-020-01016-6 |
0.38 |
|
| 2020 |
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, ... ... Fisher SE, et al. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry. PMID 33057169 DOI: 10.1038/s41380-020-00898-x |
0.72 |
|
| 2020 |
Verhoef E, Shapland CY, Fisher SE, Dale PS, St Pourcain B. The developmental origins of genetic factors influencing language and literacy: Associations with early-childhood vocabulary. Journal of Child Psychology and Psychiatry, and Allied Disciplines. PMID 32924135 DOI: 10.1111/Jcpp.13327 |
0.409 |
|
| 2020 |
Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, ... ... Fisher SE, et al. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. American Journal of Human Genetics. PMID 32891193 DOI: 10.1016/J.Ajhg.2020.08.013 |
0.357 |
|
| 2020 |
den Hoed J, Fisher SE. Genetic pathways involved in human speech disorders. Current Opinion in Genetics & Development. 65: 103-111. PMID 32622339 DOI: 10.1016/J.Gde.2020.05.012 |
0.481 |
|
| 2020 |
Kong XZ, Postema MC, Guadalupe T, de Kovel C, Boedhoe PSW, Hoogman M, Mathias SR, van Rooij D, Schijven D, Glahn DC, Medland SE, Jahanshad N, Thomopoulos SI, Turner JA, Buitelaar J, ... ... Fisher SE, et al. Mapping brain asymmetry in health and disease through the ENIGMA consortium. Human Brain Mapping. PMID 32420672 DOI: 10.1002/Hbm.25033 |
0.525 |
|
| 2020 |
Hildebrand MS, Jackson VE, Scerri TS, Van Reyk O, Coleman M, Braden RO, Turner S, Rigbye KA, Boys A, Barton S, Webster R, Fahey M, Saunders K, Parry-Fielder B, Paxton G, ... ... Fisher SE, et al. Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation. Neurology. PMID 32345733 DOI: 10.1212/WNL.0000000000009441 |
0.331 |
|
| 2020 |
Doust C, Gordon SD, Garden N, Fisher SE, Martin NG, Bates TC, Luciano M. The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-10. PMID 32248883 DOI: 10.1017/Thg.2020.7 |
0.51 |
|
| 2020 |
Thompson PM, Jahanshad N, Ching CRK, Salminen LE, Thomopoulos SI, Bright J, Baune BT, Bertolín S, Bralten J, Bruin WB, Bülow R, Chen J, Chye Y, Dannlowski U, de Kovel CGF, ... ... Fisher SE, et al. ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. Translational Psychiatry. 10: 100. PMID 32198361 DOI: 10.1038/S41398-020-0705-1 |
0.535 |
|
| 2020 |
Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, ... ... Fisher SE, et al. The genetic architecture of the human cerebral cortex. Science (New York, N.Y.). 367. PMID 32193296 DOI: 10.1126/Science.Aay6690 |
0.38 |
|
| 2020 |
Tilot AK, Vino A, Kucera KS, Carmichael DA, van den Heuvel L, den Hoed J, Sidoroff-Dorso AV, Campbell A, Porteous DJ, St Pourcain B, van Leeuwen TM, Ward J, Rouw R, Simner J, Fisher SE. Correction to 'Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits'. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 375: 20190746. PMID 32075566 DOI: 10.1098/Rstb.2019.0746 |
0.314 |
|
| 2020 |
Kong X, Tzourio-Mazoyer N, Joliot M, Fedorenko E, Liu J, Fisher SE, Francks C. Gene Expression Correlates of the Cortical Network Underlying Sentence Processing Neurobiology of Language. 1: 77-103. DOI: 10.1162/nol_a_00004 |
0.352 |
|
| 2019 |
Carrion-Castillo A, Pepe A, Kong XZ, Fisher SE, Mazoyer B, Tzourio-Mazoyer N, Crivello F, Francks C. Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 124: 137-153. PMID 31887566 DOI: 10.1016/J.Cortex.2019.11.006 |
0.555 |
|
| 2019 |
Postema MC, van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Filho GB, Calderoni S, Calvo R, Daly E, Deruelle C, Di Martino A, Dinstein I, Duran FLS, Durston S, ... ... Fisher SE, et al. Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. Nature Communications. 10: 4958. PMID 31673008 DOI: 10.1038/S41467-019-13005-8 |
0.361 |
|
| 2019 |
van der Meer D, Sønderby IE, Kaufmann T, Walters GB, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, ... ... Fisher SE, et al. Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. Jama Psychiatry. 1-11. PMID 31665216 DOI: 10.1001/Jamapsychiatry.2019.3779 |
0.349 |
|
| 2019 |
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV, Smith AV, Bis JC, Jian X, Luciano M, Hofer E, ... ... Fisher SE, et al. Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics. PMID 31636452 DOI: 10.1038/S41588-019-0511-Y |
0.411 |
|
| 2019 |
Fisher SE, Tilot AK. Bridging senses: novel insights from synaesthesia. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 374: 20190022. PMID 31630657 DOI: 10.1098/Rstb.2019.0022 |
0.33 |
|
| 2019 |
Tilot AK, Vino A, Kucera KS, Carmichael DA, van den Heuvel L, den Hoed J, Sidoroff-Dorso AV, Campbell A, Porteous DJ, St Pourcain B, van Leeuwen TM, Ward J, Rouw R, Simner J, Fisher SE. Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 374: 20190026. PMID 31630655 DOI: 10.1098/Rstb.2019.0026 |
0.41 |
|
| 2019 |
Uddén J, Hultén A, Bendtz K, Mineroff Z, Kucera KS, Vino A, Fedorenko E, Hagoort P, Fisher SE. Towards robust functional neuroimaging genetics of cognition. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31570534 DOI: 10.1523/Jneurosci.0888-19.2019 |
0.412 |
|
| 2019 |
Snijders Blok L, Kleefstra T, Venselaar H, Maas S, Kroes HY, Lachmeijer AMA, van Gassen KLI, Firth HV, Tomkins S, Bodek S, Õunap K, Wojcik MH, Cunniff C, Bergstrom K, ... ... Fisher SE, et al. De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder. American Journal of Human Genetics. PMID 31303265 DOI: 10.1016/J.Ajhg.2019.06.007 |
0.471 |
|
| 2019 |
Truong DT, Adams AK, Paniagua S, Frijters JC, Boada R, Hill DE, Lovett MW, Mahone EM, Willcutt EG, Wolf M, Defries JC, Gialluisi A, Francks C, Fisher SE, Olson RK, et al. Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Journal of Medical Genetics. PMID 30995994 DOI: 10.1136/Jmedgenet-2018-105874 |
0.322 |
|
| 2019 |
Carrion-Castillo A, Van der Haegen L, Tzourio-Mazoyer N, Kavaklioglu T, Badillo S, Chavent M, Saracco J, Brysbaert M, Fisher SE, Mazoyer B, Francks C. Genome sequencing for rightward hemispheric language dominance. Genes, Brain, and Behavior. e12572. PMID 30950222 DOI: 10.1111/Gbb.12572 |
0.443 |
|
| 2019 |
Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, ... ... Fisher SE, et al. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications. 10: 883. PMID 30770872 DOI: 10.1038/S41467-019-08800-2 |
0.34 |
|
| 2019 |
Castells-Nobau A, Eidhof I, Fenckova M, Brenman-Suttner DB, Scheffer-de Gooyert JM, Christine S, Schellevis RL, van der Laan K, Quentin C, van Ninhuijs L, Hofmann F, Ejsmont R, Fisher SE, Kramer JM, Sigrist SJ, et al. Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila. Plos One. 14: e0211652. PMID 30753188 DOI: 10.1371/Journal.Pone.0211652 |
0.381 |
|
| 2019 |
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, ... ... Fisher SE, et al. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Translational Psychiatry. 9: 77. PMID 30741946 DOI: 10.1038/S41398-019-0402-0 |
0.738 |
|
| 2019 |
Verhoef E, Demontis D, Burgess S, Shapland CY, Dale PS, Okbay A, Neale BM, Faraone SV, Stergiakouli E, Davey Smith G, Fisher SE, Børglum AD, St Pourcain B. Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language. Translational Psychiatry. 9: 35. PMID 30679418 DOI: 10.1038/S41398-018-0324-2 |
0.373 |
|
| 2019 |
Fisher SE. Human Genetics: The Evolving Story of FOXP2. Current Biology : Cb. 29: R65-R67. PMID 30668952 DOI: 10.1016/J.Cub.2018.11.047 |
0.465 |
|
| 2019 |
Haworth S, Shapland CY, Hayward C, Prins BP, Felix JF, Medina-Gomez C, Rivadeneira F, Wang C, Ahluwalia TS, Vrijheid M, Guxens M, Sunyer J, Tachmazidou I, Walter K, Iotchkova V, ... ... Fisher SE, et al. Low-frequency variation in TP53 has large effects on head circumference and intracranial volume. Nature Communications. 10: 357. PMID 30664637 DOI: 10.1038/S41467-018-07863-X |
0.341 |
|
| 2019 |
Eising E, Pourcain BS, Francks C, Fisher SE. SA89A GENOME-WIDE ASSOCIATION SCREEN OF QUANTITATIVE SPEECH, LANGUAGE AND READING TRAITS IN >14,000 PEOPLE IN THE GENLANG CONSORTIUM European Neuropsychopharmacology. 29: S1237. DOI: 10.1016/J.Euroneuro.2018.08.311 |
0.43 |
|
| 2019 |
Verhoef E, Grove J, Shapland CY, Demontis D, Burgess S, Smith GD, Rai D, Fisher SE, Børglum AD, Pourcain BS. 35Opposite Genetic Effects For Polygenic Asd Risk Shared With And Independent Of Adhd: Evidence For A Cancelling-Out Hypothesis Studying Genetic Overlap With Language And Literacy European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.042 |
0.404 |
|
| 2019 |
Schlag F, Buitelaar J, Grove J, Verhoef E, Shapland CY, Demontis D, Smith GD, Rai D, Fisher SE, Børglum A, Pourcain BS. 33Exploring The Developmental Genetic Architecture Of Social Behaviour: Evidence For Genetic Overlap With Asd And Adhd European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.040 |
0.316 |
|
| 2019 |
Verhoef E, Demontis D, Burgess S, Shapland CY, Neale BM, Faraone SV, Viechtbauer W, Ssgac, Stergiakouli E, Smith GD, Fisher SE, Børglum AD, Pourcain BS. Polygenic Risk For Adhd Is Associated With Reading And Spelling Related Traits Beyond Pleiotropic Effects Due To Educational Attainment European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.052 |
0.399 |
|
| 2019 |
Fisher S. Integrating Molecular Anthropology and Neuroimaging Genomics To Shed New Light On Human Brain Evolution European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.134 |
0.395 |
|
| 2019 |
Pourcain BS, Eaves L, Verhoef E, Shapland CY, Ring SM, Fisher SE, Medland SE, Evans D, Smith GD. Genes within the context of development: changes in genetic trait architectures during childhood and adolescence European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.071 |
0.364 |
|
| 2018 |
Gunz P, Tilot AK, Wittfeld K, Teumer A, Shapland CY, van Erp TGM, Dannemann M, Vernot B, Neubauer S, Guadalupe T, Fernández G, Brunner HG, Enard W, Fallon J, Hosten N, ... ... Fisher SE, et al. Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity. Current Biology : Cb. PMID 30554901 DOI: 10.1016/J.Cub.2018.10.065 |
0.369 |
|
| 2018 |
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, ... ... Fisher SE, et al. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications. 9: 4619. PMID 30397230 DOI: 10.1038/S41467-018-06014-6 |
0.426 |
|
| 2018 |
van der Meer D, Rokicki J, Kaufmann T, Córdova-Palomera A, Moberget T, Alnæs D, Bettella F, Frei O, Doan NT, Sønderby IE, Smeland OB, Agartz I, Bertolino A, Bralten J, Brandt CL, ... ... Fisher SE, et al. Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Molecular Psychiatry. PMID 30279459 DOI: 10.1038/S41380-018-0262-7 |
0.362 |
|
| 2018 |
den Hoed J, Sollis E, Venselaar H, Estruch SB, Deriziotis P, Fisher SE. Functional characterization of TBR1 variants in neurodevelopmental disorder. Scientific Reports. 8: 14279. PMID 30250039 DOI: 10.1038/S41598-018-32053-6 |
0.409 |
|
| 2018 |
van Rhijn JR, Fisher SE, Vernes SC, Nadif Kasri N. Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release. Brain Structure & Function. PMID 30187194 DOI: 10.1007/S00429-018-1746-6 |
0.661 |
|
| 2018 |
de Kovel CGF, Lisgo SN, Fisher SE, Francks C. Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains. Scientific Reports. 8: 12606. PMID 30181561 DOI: 10.1038/S41598-018-29496-2 |
0.367 |
|
| 2018 |
French CA, Vinueza Veloz MF, Zhou K, Peter S, Fisher SE, Costa RM, De Zeeuw CI. Differential effects of Foxp2 disruption in distinct motor circuits. Molecular Psychiatry. PMID 30108312 DOI: 10.1038/S41380-018-0199-X |
0.349 |
|
| 2018 |
Xu S, Liu P, Chen Y, Chen Y, Zhang W, Zhao H, Cao Y, Wang F, Jiang N, Lin S, Li B, Zhang Z, Wei Z, Fan Y, Jin Y, ... ... Fisher SE, et al. Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion. Proceedings of the National Academy of Sciences of the United States of America. PMID 30104377 DOI: 10.1073/Pnas.1721820115 |
0.479 |
|
| 2018 |
Kong XZ, Mathias SR, Guadalupe T, Glahn DC, Franke B, Crivello F, Tzourio-Mazoyer N, Fisher SE, Thompson PM, Francks C. Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium. Proceedings of the National Academy of Sciences of the United States of America. PMID 29764998 DOI: 10.1073/pnas.1718418115 |
0.468 |
|
| 2018 |
Snijders Blok L, Hiatt SM, Bowling KM, Prokop JW, Engel KL, Cochran JN, Bebin EM, Bijlsma EK, Ruivenkamp CAL, Terhal P, Simon MEH, Smith R, Hurst JA, McLaughlin H, ... ... Fisher SE, et al. De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder. Human Genetics. PMID 29740699 DOI: 10.1007/S00439-018-1887-Y |
0.39 |
|
| 2018 |
Becker M, Devanna P, Fisher SE, Vernes SC. Mapping of HumanEnhancers Reveals Complex Regulation. Frontiers in Molecular Neuroscience. 11: 47. PMID 29515369 DOI: 10.3389/Fnmol.2018.00047 |
0.736 |
|
| 2018 |
Tilot AK, Kucera KS, Vino A, Asher JE, Baron-Cohen S, Fisher SE. Rare variants in axonogenesis genes connect three families with sound-color synesthesia. Proceedings of the National Academy of Sciences of the United States of America. PMID 29507195 DOI: 10.1073/Pnas.1715492115 |
0.421 |
|
| 2018 |
Eising E, Carrion-Castillo A, Vino A, Strand EA, Jakielski KJ, Scerri TS, Hildebrand MS, Webster R, Ma A, Mazoyer B, Francks C, Bahlo M, Scheffer IE, Morgan AT, Shriberg LD, ... Fisher SE, et al. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Molecular Psychiatry. PMID 29463886 DOI: 10.1038/S41380-018-0020-X |
0.505 |
|
| 2018 |
Mei C, Fedorenko E, Amor DJ, Boys A, Hoeflin C, Carew P, Burgess T, Fisher SE, Morgan AT. Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion. European Journal of Human Genetics : Ejhg. PMID 29445122 DOI: 10.1038/S41431-018-0102-X |
0.445 |
|
| 2018 |
Estruch SB, Graham SA, Quevedo M, Vino A, Dekkers DHW, Deriziotis P, Sollis E, Demmers J, Poot RA, Fisher SE. Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders. Human Molecular Genetics. PMID 29365100 DOI: 10.1093/Hmg/Ddy035 |
0.356 |
|
| 2017 |
Kuerbitz J, Arnett MG, Ehrman S, Williams MT, Vorhees CV, Fisher SE, Garratt AN, Muglia LJ, Waclaw RR, Campbell K. Loss of intercalated cells (ITCs) in the mouse amygdala of Tshz1 mutants correlates with fear, depression and social interaction phenotypes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29255003 DOI: 10.1523/Jneurosci.1412-17.2017 |
0.312 |
|
| 2017 |
Morgan AT, Haaften LV, van Hulst K, Edley C, Mei C, Tan TY, Amor D, Fisher SE, Koolen DA. Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia. European Journal of Human Genetics : Ejhg. PMID 29225339 DOI: 10.1038/S41431-017-0035-9 |
0.444 |
|
| 2017 |
St Pourcain B, Eaves LJ, Ring SM, Fisher SE, Medland S, Evans DM, Davey Smith G. Developmental Changes Within the Genetic Architecture of Social Communication Behavior: A Multivariate Study of Genetic Variance in Unrelated Individuals. Biological Psychiatry. PMID 29100628 DOI: 10.1016/J.Biopsych.2017.09.020 |
0.349 |
|
| 2017 |
Zubicaray G, Fisher SE. Genes, Brain, and Language: A brief introduction to the Special Issue. Brain and Language. 172: 1-2. PMID 28867043 DOI: 10.1016/J.Bandl.2017.08.003 |
0.49 |
|
| 2017 |
Deriziotis P, Fisher SE. Speech and Language: Translating the Genome. Trends in Genetics : Tig. PMID 28781152 DOI: 10.1016/J.Tig.2017.07.002 |
0.497 |
|
| 2017 |
Sollis E, Deriziotis P, Saitsu H, Miyake N, Matsumoto N, Hoffer MJV, Ruivenkamp CAL, Alders M, Okamoto N, Bijlsma EK, Plomp AS, Fisher SE. Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Human Mutation. PMID 28741757 DOI: 10.1002/Humu.23303 |
0.463 |
|
| 2017 |
Chen XS, Reader RH, Hoischen A, Veltman JA, Simpson NH, Francks C, Newbury DF, Fisher SE. Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment. Scientific Reports. 7: 46105. PMID 28440294 DOI: 10.1038/Srep46105 |
0.5 |
|
| 2017 |
Stergiakouli E, Davey Smith G, Martin J, Skuse DH, Viechtbauer W, Ring SM, Ronald A, Evans DE, Fisher SE, Thapar A, St Pourcain B. Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development. Molecular Autism. 8: 18. PMID 28392908 DOI: 10.1186/S13229-017-0131-2 |
0.321 |
|
| 2017 |
Devanna P, Chen XS, Ho J, Gajewski D, Smith SD, Gialluisi A, Francks C, Fisher SE, Newbury DF, Vernes SC. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders. Molecular Psychiatry. PMID 28289279 DOI: 10.1038/Mp.2017.30 |
0.726 |
|
| 2017 |
de Kovel CG, Lisgo S, Karlebach G, Ju J, Cheng G, Fisher SE, Francks C. Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development. Biological Psychiatry. PMID 28267988 DOI: 10.1016/J.Euroneuro.2017.08.035 |
0.306 |
|
| 2017 |
Hibar DP, Adams HH, Jahanshad N, Chauhan G, Stein JL, Hofer E, Renteria ME, Bis JC, Arias-Vasquez A, Ikram MK, Desrivières S, Vernooij MW, Abramovic L, Alhusaini S, Amin N, ... ... Fisher SE, et al. Novel genetic loci associated with hippocampal volume. Nature Communications. 8: 13624. PMID 28098162 DOI: 10.1038/Ncomms13624 |
0.376 |
|
| 2017 |
Carrion-Castillo A, Maassen B, Franke B, Heister A, Naber M, van der Leij A, Francks C, Fisher SE. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European Journal of Human Genetics : Ejhg. PMID 28074887 DOI: 10.1038/Ejhg.2016.194 |
0.417 |
|
| 2017 |
St Pourcain B, Robinson EB, Anttila V, Sullivan BB, Maller J, Golding J, Skuse D, Ring S, Evans DM, Zammit S, Fisher SE, Neale BM, Anney RJ, Ripke S, Hollegaard MV, et al. ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties. Molecular Psychiatry. PMID 28044064 DOI: 10.1038/Mp.2016.198 |
0.316 |
|
| 2017 |
Pourcain BS, Verhoef E, Fisher SE, Stergiakouli E, Evans DE, Ring SM, Smith GD. Common Polygenic Risk For ASD And ADHD is Associated with Childhood Linguistic Traits within The General Population, But with Opposite Effects European Neuropsychopharmacology. 27: S420-S421. DOI: 10.1016/J.Euroneuro.2016.09.470 |
0.313 |
|
| 2017 |
Pourcain BS, Eaves L, Evans DM, Stergiakouli E, Fisher SE, Ring SM, Carey G, George DS. Trait-Specific Patterns Of Common Genetic Factors Influence Social-Communication Difficulties And Adhd Symptoms During Child And Adolescent Development European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.411 |
0.337 |
|
| 2016 |
Estruch SB, Graham SA, Chinnappa SM, Deriziotis P, Fisher SE. Functional characterization of rare FOXP2 variants in neurodevelopmental disorder. Journal of Neurodevelopmental Disorders. 8: 44. PMID 27933109 DOI: 10.1186/S11689-016-9177-2 |
0.464 |
|
| 2016 |
Chabout J, Sarkar A, Patel SR, Radden T, Dunson DB, Fisher SE, Jarvis ED. A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice. Frontiers in Behavioral Neuroscience. 10: 197. PMID 27812326 DOI: 10.3389/Fnbeh.2016.00197 |
0.413 |
|
| 2016 |
Guadalupe T, Mathias SR, vanErp TG, Whelan CD, Zwiers MP, Abe Y, Abramovic L, Agartz I, Andreassen OA, Arias-Vásquez A, Aribisala BS, Armstrong NJ, Arolt V, Artiges E, Ayesa-Arriola R, ... ... Fisher SE, et al. Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior. PMID 27738994 DOI: 10.1007/S11682-016-9629-Z |
0.373 |
|
| 2016 |
Adams HH, Hibar DP, Chouraki V, Stein JL, Nyquist PA, Rentería ME, Trompet S, Arias-Vasquez A, Seshadri S, Desrivières S, Beecham AH, Jahanshad N, Wittfeld K, Van der Lee SJ, Abramovic L, ... ... Fisher SE, et al. Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience. PMID 27694991 DOI: 10.1038/Nn.4398 |
0.401 |
|
| 2016 |
Kavaklioglu T, Guadalupe T, Zwiers M, Marquand AF, Onnink M, Shumskaya E, Brunner H, Fernandez G, Fisher SE, Francks C. Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness. Brain Structure & Function. PMID 27566607 DOI: 10.1007/S00429-016-1295-9 |
0.391 |
|
| 2016 |
Gialluisi A, Guadalupe T, Francks C, Fisher SE. Neuroimaging genetic analyses of novel candidate genes associated with reading and language. Brain and Language. PMID 27476042 DOI: 10.1016/J.Bandl.2016.07.002 |
0.483 |
|
| 2016 |
Dias C, Estruch SB, Graham SA, McRae J, Sawiak SJ, Hurst JA, Joss SK, Holder SE, Morton JE, Turner C, Thevenon J, Mellul K, Sánchez-Andrade G, Ibarra-Soria X, Deriziotis P, ... ... Fisher SE, et al. BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription. American Journal of Human Genetics. PMID 27453576 DOI: 10.1016/J.Ajhg.2016.05.030 |
0.416 |
|
| 2016 |
Fisher SE. Evolution of language: Lessons from the genome. Psychonomic Bulletin & Review. PMID 27432000 DOI: 10.3758/S13423-016-1112-8 |
0.463 |
|
| 2016 |
Woo YJ, Wang T, Guadalupe T, Nebel RA, Vino A, Del Bene VA, Molholm S, Ross LA, Zwiers MP, Fisher SE, Foxe JJ, Abrahams BS. A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus. Plos One. 11: e0158036. PMID 27351196 DOI: 10.1371/Journal.Pone.0158036 |
0.495 |
|
| 2016 |
Carrion-Castillo A, van Bergen E, Vino A, van Zuijen T, de Jong PF, Francks C, Fisher SE. Evaluation of results from genome-wide studies of language and reading in a novel independent dataset. Genes, Brain, and Behavior. PMID 27198479 DOI: 10.1111/Gbb.12299 |
0.436 |
|
| 2016 |
Gialluisi A, Visconti A, Willcutt EG, Smith SD, Pennington BF, Falchi M, DeFries JC, Olson RK, Francks C, Fisher SE. Investigating the effects of copy number variants on reading and language performance. Journal of Neurodevelopmental Disorders. 8: 17. PMID 27186239 DOI: 10.1186/S11689-016-9147-8 |
0.446 |
|
| 2016 |
Uddén J, Snijders TM, Fisher SE, Hagoort P. A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus. Brain and Language. PMID 27059522 DOI: 10.1016/J.Bandl.2016.02.003 |
0.408 |
|
| 2016 |
Becker M, Guadalupe T, Franke B, Hibar DP, Renteria ME, Stein JL, Thompson PM, Francks C, Vernes SC, Fisher SE. Early developmental gene enhancers affect subcortical volumes in the adult human brain. Human Brain Mapping. PMID 26890892 DOI: 10.1002/Hbm.23136 |
0.712 |
|
| 2016 |
Estruch SB, Graham SA, Deriziotis P, Fisher SE. The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers. Scientific Reports. 6: 20911. PMID 26867680 DOI: 10.1038/Srep20911 |
0.43 |
|
| 2015 |
Thompson PM, Andreassen OA, Arias-Vasquez A, Bearden CE, Boedhoe PS, Brouwer RM, Buckner RL, Buitelaar JK, Bulaeva KB, Cannon DM, Cohen RA, Conrod PJ, Dale AM, Deary IJ, Dennis EL, ... ... Fisher SE, et al. ENIGMA and the Individual: Predicting Factors that Affect the Brain in 35 Countries Worldwide. Neuroimage. PMID 26658930 DOI: 10.1016/J.Neuroimage.2015.11.057 |
0.346 |
|
| 2015 |
Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE. Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. Human Molecular Genetics. PMID 26647308 DOI: 10.1093/Hmg/Ddv495 |
0.483 |
|
| 2015 |
Gaub S, Fisher SE, Ehret G. Ultrasonic vocalizations of adult male Foxp2-mutant mice: behavioral contexts of arousal and emotion. Genes, Brain, and Behavior. PMID 26566793 DOI: 10.1111/Gbb.12274 |
0.334 |
|
| 2015 |
Graham SA, Fisher SE. Understanding Language from a Genomic Perspective. Annual Review of Genetics. PMID 26442845 DOI: 10.1146/Annurev-Genet-120213-092236 |
0.505 |
|
| 2015 |
Becker M, Devanna P, Fisher SE, Vernes SC. A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer. Molecular Cytogenetics. 8: 69. PMID 26300977 DOI: 10.1186/S13039-015-0173-0 |
0.742 |
|
| 2015 |
Chen J, Calhoun VD, Arias-Vasquez A, Zwiers MP, van Hulzen K, Fernández G, Fisher SE, Franke B, Turner JA, Liu J. G-protein genomic association with normal variation in gray matter density. Human Brain Mapping. PMID 26248772 DOI: 10.1002/Hbm.22916 |
0.392 |
|
| 2015 |
Warrier V, Chakrabarti B, Murphy L, Chan A, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Baron-Cohen S. A Pooled Genome-Wide Association Study of Asperger Syndrome. Plos One. 10: e0131202. PMID 26176695 DOI: 10.1371/Journal.Pone.0131202 |
0.373 |
|
| 2015 |
Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N. A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. European Journal of Human Genetics : Ejhg. PMID 26173965 DOI: 10.1038/Ejhg.2015.149 |
0.429 |
|
| 2015 |
Gascoyne DM, Spearman H, Lyne L, Puliyadi R, Perez-Alcantara M, Coulton L, Fisher SE, Croucher PI, Banham AH. The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest. Plos One. 10: e0128513. PMID 26034982 DOI: 10.1371/Journal.Pone.0128513 |
0.335 |
|
| 2015 |
Lozano R, Vino A, Lozano C, Fisher SE, Deriziotis P. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment. European Journal of Human Genetics : Ejhg. PMID 25853299 DOI: 10.1038/Ejhg.2015.66 |
0.513 |
|
| 2015 |
Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Echeverry MM, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER, ... ... Fisher SE, et al. Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. Plos Genetics. 11: e1004925. PMID 25781923 DOI: 10.1371/Journal.Pgen.1004925 |
0.454 |
|
| 2015 |
Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE, Whitehouse AJ, Snowling MJ, et al. Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. Genes, Brain, and Behavior. 14: 369-76. PMID 25778778 DOI: 10.1111/Gbb.12213 |
0.675 |
|
| 2015 |
Brucato N, Guadalupe T, Franke B, Fisher SE, Francks C. A schizophrenia-associated HLA locus affects thalamus volume and asymmetry. Brain, Behavior, and Immunity. 46: 311-8. PMID 25728236 DOI: 10.1016/J.Bbi.2015.02.021 |
0.349 |
|
| 2015 |
Gingras B, Honing H, Peretz I, Trainor LJ, Fisher SE. Defining the biological bases of individual differences in musicality. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 370: 20140092. PMID 25646515 DOI: 10.1098/Rstb.2014.0092 |
0.428 |
|
| 2015 |
Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, ... ... Fisher SE, et al. Common genetic variants influence human subcortical brain structures. Nature. 520: 224-9. PMID 25607358 DOI: 10.1038/Nature14101 |
0.392 |
|
| 2015 |
Graham SA, Deriziotis P, Fisher SE. Insights into the genetic foundations of human communication. Neuropsychology Review. 25: 3-26. PMID 25597031 DOI: 10.1007/S11065-014-9277-2 |
0.483 |
|
| 2015 |
Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC, Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF. Genome-wide analysis identifies a role for common copy number variants in specific language impairment. European Journal of Human Genetics : Ejhg. PMID 25585696 DOI: 10.1038/Ejhg.2014.296 |
0.459 |
|
| 2015 |
Guadalupe T, Zwiers MP, Wittfeld K, Teumer A, Vasquez AA, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, van Bokhoven H, Hegenscheid K, Völzke H, Franke B, Fisher SE, Grabe HJ, et al. Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 62: 41-55. PMID 25239853 DOI: 10.1016/J.Cortex.2014.07.015 |
0.399 |
|
| 2015 |
Fisher SE, Vernes SC. Genetics and the Language Sciences Annual Review of Linguistics. 1: 289-310. DOI: 10.1146/annurev-linguist-030514-125024 |
0.723 |
|
| 2014 |
Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H, Parr J, ... ... Fisher SE, et al. Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' European Journal of Human Genetics : Ejhg. PMID 25537359 DOI: 10.1038/Ejhg.2014.275 |
0.393 |
|
| 2014 |
Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE. De novo TBR1 mutations in sporadic autism disrupt protein functions. Nature Communications. 5: 4954. PMID 25232744 DOI: 10.1038/Ncomms5954 |
0.418 |
|
| 2014 |
Schreiweis C, Bornschein U, Burguière E, Kerimoglu C, Schreiter S, Dannemann M, Goyal S, Rea E, French CA, Puliyadi R, Groszer M, Fisher SE, Mundry R, Winter C, Hevers W, et al. Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance. Proceedings of the National Academy of Sciences of the United States of America. 111: 14253-8. PMID 25225386 DOI: 10.1073/Pnas.1414542111 |
0.432 |
|
| 2014 |
Cousijn H, Eissing M, Fernández G, Fisher SE, Franke B, Zwiers M, Harrison PJ, Arias-Vásquez A. No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. Schizophrenia Research. 159: 329-32. PMID 25217366 DOI: 10.1016/J.Schres.2014.08.007 |
0.326 |
|
| 2014 |
Cai DC, Fonteijn H, Guadalupe T, Zwiers M, Wittfeld K, Teumer A, Hoogman M, Arias-Vásquez A, Yang Y, Buitelaar J, Fernández G, Brunner HG, van Bokhoven H, Franke B, Hegenscheid K, ... ... Fisher SE, et al. A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus. Genes, Brain, and Behavior. 13: 675-85. PMID 25130324 DOI: 10.1111/Gbb.12157 |
0.395 |
|
| 2014 |
Brucato N, DeLisi LE, Fisher SE, Francks C. Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 555-63. PMID 25111784 DOI: 10.1002/Ajmg.B.32258 |
0.339 |
|
| 2014 |
Gialluisi A, Newbury DF, Wilcutt EG, Olson RK, DeFries JC, Brandler WM, Pennington BF, Smith SD, Scerri TS, Simpson NH, Luciano M, Evans DM, Bates TC, Stein JF, ... ... Fisher SE, et al. Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain, and Behavior. 13: 686-701. PMID 25065397 DOI: 10.1111/Gbb.12158 |
0.76 |
|
| 2014 |
French CA, Fisher SE. What can mice tell us about Foxp2 function? Current Opinion in Neurobiology. 28: 72-9. PMID 25048596 DOI: 10.1016/J.Conb.2014.07.003 |
0.427 |
|
| 2014 |
Hoogman M, Guadalupe T, Zwiers MP, Klarenbeek P, Francks C, Fisher SE. Assessing the effects of common variation in the FOXP2 gene on human brain structure. Frontiers in Human Neuroscience. 8: 473. PMID 25013396 DOI: 10.3389/Fnhum.2014.00473 |
0.406 |
|
| 2014 |
Guadalupe T, Zwiers MP, Teumer A, Wittfeld K, Vasquez AA, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Hegenscheid K, Völzke H, Franke B, Fisher SE, Grabe HJ, Francks C. Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets. Human Brain Mapping. 35: 3277-89. PMID 24827550 DOI: 10.1002/Hbm.22401 |
0.367 |
|
| 2014 |
Baron-Cohen S, Murphy L, Chakrabarti B, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Warrier V. A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. Plos One. 9: e96374. PMID 24801482 DOI: 10.1371/Journal.Pone.0096374 |
0.381 |
|
| 2014 |
Guadalupe T, Willems RM, Zwiers MP, Arias Vasquez A, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Franke B, Fisher SE, Francks C. Differences in cerebral cortical anatomy of left- and right-handers. Frontiers in Psychology. 5: 261. PMID 24734025 DOI: 10.3389/Fpsyg.2014.00261 |
0.324 |
|
| 2014 |
Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Genes, Brain, and Behavior. 13: 418-29. PMID 24571439 DOI: 10.1111/Gbb.12127 |
0.743 |
|
| 2014 |
Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H, Parr J, ... ... Fisher SE, et al. Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. European Journal of Human Genetics : Ejhg. 22: 1165-71. PMID 24518835 DOI: 10.1038/Ejhg.2014.4 |
0.493 |
|
| 2014 |
Willems RM, Van der Haegen L, Fisher SE, Francks C. On the other hand: including left-handers in cognitive neuroscience and neurogenetics. Nature Reviews. Neuroscience. 15: 193-201. PMID 24518415 DOI: 10.1038/Nrn3679 |
0.338 |
|
| 2014 |
Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF. Associations of HLA alleles with specific language impairment. Journal of Neurodevelopmental Disorders. 6: 1. PMID 24433325 DOI: 10.1186/1866-1955-6-1 |
0.571 |
|
| 2014 |
Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, Toro R, Jahanshad N, Schumann G, Franke B, Wright MJ, Martin NG, Agartz I, Alda M, Alhusaini S, ... ... Fisher SE, et al. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 8: 153-82. PMID 24399358 DOI: 10.1007/S11682-013-9269-5 |
0.369 |
|
| 2014 |
Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, ... ... Fisher SE, et al. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine and Child Neurology. 56: 346-53. PMID 24117048 DOI: 10.1111/Dmcn.12294 |
0.697 |
|
| 2013 |
Baron-Cohen S, Johnson D, Asher J, Wheelwright S, Fisher SE, Gregersen PK, Allison C. Is synaesthesia more common in autism? Molecular Autism. 4: 40. PMID 24252644 DOI: 10.1186/2040-2392-4-40 |
0.324 |
|
| 2013 |
Carrion-Castillo A, Franke B, Fisher SE. Molecular genetics of dyslexia: an overview. Dyslexia (Chichester, England). 19: 214-40. PMID 24133036 DOI: 10.1002/Dys.1464 |
0.396 |
|
| 2013 |
Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S. Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Plos Genetics. 9: e1003751. PMID 24068947 DOI: 10.1371/Journal.Pgen.1003751 |
0.738 |
|
| 2013 |
Fisher SE, Ridley M. Evolution. Culture, genes, and the human revolution. Science (New York, N.Y.). 340: 929-30. PMID 23704558 DOI: 10.1126/Science.1236171 |
0.328 |
|
| 2013 |
Ayub Q, Yngvadottir B, Chen Y, Xue Y, Hu M, Vernes SC, Fisher SE, Tyler-Smith C. FOXP2 targets show evidence of positive selection in European populations. American Journal of Human Genetics. 92: 696-706. PMID 23602712 DOI: 10.1016/J.Ajhg.2013.03.019 |
0.718 |
|
| 2013 |
Deriziotis P, Fisher SE. Neurogenomics of speech and language disorders: the road ahead. Genome Biology. 14: 204. PMID 23597266 DOI: 10.1186/Gb-2013-14-4-204 |
0.443 |
|
| 2013 |
Gregersen PK, Kowalsky E, Lee A, Baron-Cohen S, Fisher SE, Asher JE, Ballard D, Freudenberg J, Li W. Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Human Molecular Genetics. 22: 2097-104. PMID 23406871 DOI: 10.1093/Hmg/Ddt059 |
0.369 |
|
| 2013 |
Gialluisi A, Dediu D, Francks C, Fisher SE. Persistence and transmission of recessive deafness and sign language: new insights from village sign languages. European Journal of Human Genetics : Ejhg. 21: 894-6. PMID 23321624 DOI: 10.1038/Ejhg.2012.292 |
0.406 |
|
| 2013 |
Graham SA, Fisher SE. Decoding the genetics of speech and language. Current Opinion in Neurobiology. 23: 43-51. PMID 23228431 DOI: 10.1016/J.Conb.2012.11.006 |
0.513 |
|
| 2013 |
Newbury DF, Mari F, Sadighi Akha E, Macdermot KD, Canitano R, Monaco AP, Taylor JC, Renieri A, Fisher SE, Knight SJ. Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. European Journal of Human Genetics : Ejhg. 21: 361-5. PMID 22909776 DOI: 10.1038/Ejhg.2012.166 |
0.524 |
|
| 2013 |
Cai D, Fonteijn H, Guadalupe T, Zwiers M, Hoogman M, Vásquez AA, Yang Y, Buitelaar J, Fernández G, Brunner HG, Bokhoven HV, Franke B, Fisher SE, Francks C, Hagoort P. Genome-wide search shows association between 10p15.2 and the volume of left Heschl's Gyrus F1000research. 4. DOI: 10.7490/F1000Research.1093633.1 |
0.306 |
|
| 2013 |
Vernes SC, Fisher SE. Genetic pathways implicated in speech and language Animal Models of Speech and Language Disorders. 13-40. DOI: 10.1007/978-1-4614-8400-4_2 |
0.697 |
|
| 2012 |
Walker RM, Hill AE, Newman AC, Hamilton G, Torrance HS, Anderson SM, Ogawa F, Derizioti P, Nicod J, Vernes SC, Fisher SE, Thomson PA, Porteous DJ, Evans KL. The DISC1 promoter: characterization and regulation by FOXP2. Human Molecular Genetics. 21: 2862-72. PMID 22434823 DOI: 10.1093/Hmg/Dds111 |
0.717 |
|
| 2012 |
Kurt S, Fisher SE, Ehret G. Foxp2 mutations impair auditory-motor association learning. Plos One. 7: e33130. PMID 22412993 DOI: 10.1371/Journal.Pone.0033130 |
0.429 |
|
| 2012 |
French CA, Jin X, Campbell TG, Gerfen E, Groszer M, Fisher SE, Costa RM. An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning. Molecular Psychiatry. 17: 1077-85. PMID 21876543 DOI: 10.1038/Mp.2011.105 |
0.377 |
|
| 2012 |
Whitehouse AJO, Bishop DVM, Ang QW, Pennell CE, Fisher SE. CNTNAP2 variants affect early language development in the general population Genes, Brain and Behavior. 11: 501. DOI: 10.1111/J.1601-183X.2012.00806.X |
0.386 |
|
| 2012 |
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, MacKenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Corrigendum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations (Nature Genetics (2011) 43, (585-589)) Nature Genetics. 44: 471. DOI: 10.1038/Ng0412-471 |
0.365 |
|
| 2011 |
Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, ... ... Fisher SE, et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Plos Genetics. 7: e1002145. PMID 21765815 DOI: 10.1371/Journal.Pgen.1002145 |
0.757 |
|
| 2011 |
O'Roak BJ, Deriziotis P, Lee C, Vives L, Schwartz JJ, Girirajan S, Karakoc E, Mackenzie AP, Ng SB, Baker C, Rieder MJ, Nickerson DA, Bernier R, Fisher SE, Shendure J, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics. 43: 585-9. PMID 21572417 DOI: 10.1038/Ng.835 |
0.369 |
|
| 2011 |
Whitehouse AJ, Bishop DV, Ang QW, Pennell CE, Fisher SE. CNTNAP2 variants affect early language development in the general population. Genes, Brain, and Behavior. 10: 451-6. PMID 21310003 DOI: 10.1111/J.1601-183X.2011.00684.X |
0.475 |
|
| 2011 |
Fisher SE. GL.03 Molecular windows into speech and language disorders Journal of Neurology, Neurosurgery & Psychiatry. 82: e2-e2. DOI: 10.1136/Jnnp-2011-300504.23 |
0.514 |
|
| 2010 |
Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, Massacrier A, Rudolf G, Khalife M, Hirsch E, Fisher SE, Szepetowski P. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Human Molecular Genetics. 19: 4848-60. PMID 20858596 DOI: 10.1093/Hmg/Ddq415 |
0.709 |
|
| 2010 |
Newbury DF, Fisher SE, Monaco AP. Recent advances in the genetics of language impairment. Genome Medicine. 2: 6. PMID 20193051 DOI: 10.1186/Gm127 |
0.612 |
|
| 2010 |
Fisher SE. Genetic susceptibility to stuttering. The New England Journal of Medicine. 362: 750-2. PMID 20147708 DOI: 10.1056/Nejme0912594 |
0.471 |
|
| 2010 |
Gaub S, Groszer M, Fisher SE, Ehret G. The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes, Brain, and Behavior. 9: 390-401. PMID 20132318 DOI: 10.1111/J.1601-183X.2010.00570.X |
0.418 |
|
| 2010 |
French CA, Jin X, Campbell TG, Gerfen E, Groszer M, Fisher SE. Aberrant striatal activity in mice with a mutation implicated in a developmental speech and language disorder International Journal of Developmental Neuroscience. 28: 694-695. DOI: 10.1016/J.Ijdevneu.2010.07.154 |
0.421 |
|
| 2009 |
Vernes SC, Fisher SE. Unravelling neurogenetic networks implicated in developmental language disorders. Biochemical Society Transactions. 37: 1263-9. PMID 19909259 DOI: 10.1042/Bst0371263 |
0.759 |
|
| 2009 |
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, ... ... Fisher SE, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American Journal of Human Genetics. 85: 264-72. PMID 19646677 DOI: 10.1016/J.Ajhg.2009.07.004 |
0.749 |
|
| 2009 |
Kurt S, Groszer M, Fisher SE, Ehret G. Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain Research. 1289: 30-6. PMID 19596273 DOI: 10.1016/J.Brainres.2009.06.092 |
0.442 |
|
| 2009 |
Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK, Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U, ... ... Fisher SE, et al. A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell. 137: 961-71. PMID 19490899 DOI: 10.1016/J.Cell.2009.03.041 |
0.4 |
|
| 2009 |
Vernes SC, MacDermot KD, Monaco AP, Fisher SE. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European Journal of Human Genetics : Ejhg. 17: 1354-8. PMID 19352412 DOI: 10.1038/Ejhg.2009.43 |
0.779 |
|
| 2009 |
Fisher SE, Scharff C. FOXP2 as a molecular window into speech and language. Trends in Genetics : Tig. 25: 166-77. PMID 19304338 DOI: 10.1016/J.Tig.2009.03.002 |
0.705 |
|
| 2008 |
Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. A functional genetic link between distinct developmental language disorders. The New England Journal of Medicine. 359: 2337-45. PMID 18987363 DOI: 10.1056/Nejmoa0802828 |
0.811 |
|
| 2008 |
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, ... ... Fisher SE, et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Current Biology : Cb. 18: 354-62. PMID 18328704 DOI: 10.1016/J.Cub.2008.01.060 |
0.416 |
|
| 2008 |
Falcaro M, Pickles A, Newbury DF, Addis L, Banfield E, Fisher SE, Monaco AP, Simkin Z, Conti-Ramsden G. Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes, Brain, and Behavior. 7: 393-402. PMID 18005161 DOI: 10.1111/J.1601-183X.2007.00364.X |
0.547 |
|
| 2007 |
Vernes SC, Spiteri E, Nicod J, Groszer M, Taylor JM, Davies KE, Geschwind DH, Fisher SE. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American Journal of Human Genetics. 81: 1232-50. PMID 17999362 DOI: 10.1086/522238 |
0.783 |
|
| 2007 |
Spiteri E, Konopka G, Coppola G, Bomar J, Oldham M, Ou J, Vernes SC, Fisher SE, Ren B, Geschwind DH. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. American Journal of Human Genetics. 81: 1144-57. PMID 17999357 DOI: 10.1086/522237 |
0.716 |
|
| 2007 |
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Fisher SE, et al. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry. 12: 1129-39, 1057. PMID 17667961 DOI: 10.1038/Sj.Mp.4002053 |
0.776 |
|
| 2007 |
French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. Generation of mice with a conditional Foxp2 null allele. Genesis (New York, N.Y. : 2000). 45: 440-6. PMID 17619227 DOI: 10.1002/Dvg.20305 |
0.38 |
|
| 2007 |
Fisher SE. Molecular windows into speech and language disorders. Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (Ialp). 59: 130-40. PMID 17556856 DOI: 10.1016/J.Ijdevneu.2006.09.014 |
0.486 |
|
| 2007 |
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, ... ... Fisher SE, et al. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells Molecular Psychiatry. 12: 1057. DOI: 10.1038/Sj.Mp.4002116 |
0.703 |
|
| 2006 |
White SA, Fisher SE, Geschwind DH, Scharff C, Holy TE. Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10376-9. PMID 17035521 DOI: 10.1523/Jneurosci.3379-06.2006 |
0.69 |
|
| 2006 |
Vernes SC, Nicod J, Elahi FM, Coventry JA, Kenny N, Coupe AM, Bird LE, Davies KE, Fisher SE. Functional genetic analysis of mutations implicated in a human speech and language disorder. Human Molecular Genetics. 15: 3154-67. PMID 16984964 DOI: 10.1093/Hmg/Ddl392 |
0.766 |
|
| 2006 |
Fisher SE. Tangled webs: tracing the connections between genes and cognition. Cognition. 101: 270-97. PMID 16764847 DOI: 10.1016/J.Cognition.2006.04.004 |
0.435 |
|
| 2006 |
Fisher SE, Francks C. Genes, cognition and dyslexia: learning to read the genome. Trends in Cognitive Sciences. 10: 250-7. PMID 16675285 DOI: 10.1016/J.Tics.2006.04.003 |
0.411 |
|
| 2006 |
Fisher SE, Marcus GF. The eloquent ape: genes, brains and the evolution of language. Nature Reviews. Genetics. 7: 9-20. PMID 16369568 DOI: 10.1038/Nrg1747 |
0.469 |
|
| 2006 |
Ogdie MN, Bakker SC, Fisher SE, Francks C, Yang MH, Cantor RM, Loo SK, van der Meulen E, Pearson P, Buitelaar J, Monaco A, Nelson SF, Sinke RJ, Smalley SL. Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13. Molecular Psychiatry. 11: 5-8. PMID 16205734 DOI: 10.1038/Sj.Mp.4001760 |
0.506 |
|
| 2005 |
Fisher SE. On genes, speech, and language. The New England Journal of Medicine. 353: 1655-7. PMID 16236736 DOI: 10.1056/Nejmp058207 |
0.481 |
|
| 2005 |
Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC. Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 46: 1045-56. PMID 16178928 DOI: 10.1111/J.1469-7610.2005.01447.X |
0.531 |
|
| 2005 |
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics. 76: 1074-80. PMID 15877281 DOI: 10.1086/430841 |
0.78 |
|
| 2005 |
Fisher SE. Dissection of molecular mechanisms underlying speech and language disorders Applied Psycholinguistics. 26: 111-128. DOI: 10.1017/S0142716405050095 |
0.502 |
|
| 2004 |
Scerri TS, Fisher SE, Francks C, MacPhie IL, Paracchini S, Richardson AJ, Stein JF, Monaco AP. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. Journal of Medical Genetics. 41: 853-7. PMID 15520411 DOI: 10.1136/Jmg.2004.018341 |
0.718 |
|
| 2004 |
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American Journal of Human Genetics. 75: 1046-58. PMID 15514892 DOI: 10.1086/426404 |
0.724 |
|
| 2004 |
Ogdie MN, Fisher SE, Yang M, Ishii J, Francks C, Loo SK, Cantor RM, McCracken JT, McGough JJ, Smalley SL, Nelson SF. Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. American Journal of Human Genetics. 75: 661-8. PMID 15297934 DOI: 10.1086/424387 |
0.339 |
|
| 2004 |
Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects. Molecular Psychiatry. 9: 485-93. PMID 14625563 DOI: 10.1038/Sj.Mp.4001450 |
0.549 |
|
| 2003 |
Francks C, Fisher SE, Marlow AJ, MacPhie IL, Taylor KE, Richardson AJ, Stein JF, Monaco AP. Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American Journal of Psychiatry. 160: 1970-7. PMID 14594743 DOI: 10.1176/Appi.Ajp.160.11.1970 |
0.506 |
|
| 2003 |
Francks C, DeLisi LE, Shaw SH, Fisher SE, Richardson AJ, Stein JF, Monaco AP. Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human Molecular Genetics. 12: 3225-30. PMID 14583442 DOI: 10.1093/Hmg/Ddg362 |
0.507 |
|
| 2003 |
Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a Journal of Neurology. 126: 2455-62. PMID 12876151 DOI: 10.1093/Brain/Awg247 |
0.6 |
|
| 2003 |
Marcus GF, Fisher SE. FOXP2 in focus: what can genes tell us about speech and language? Trends in Cognitive Sciences. 7: 257-262. PMID 12804692 DOI: 10.1016/S1364-6613(03)00104-9 |
0.476 |
|
| 2003 |
Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C, Cantor RM, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American Journal of Human Genetics. 72: 1268-79. PMID 12687500 DOI: 10.1086/375139 |
0.524 |
|
| 2003 |
Francks C, DeLisi LE, Fisher SE, Laval SH, Rue JE, Stein JF, Monaco AP. Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American Journal of Human Genetics. 72: 499-502. PMID 12596796 DOI: 10.1086/367548 |
0.498 |
|
| 2003 |
Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ, Talcott JB, Stein JF, Monaco AP, Cardon LR. Use of multivariate linkage analysis for dissection of a complex cognitive trait. American Journal of Human Genetics. 72: 561-70. PMID 12587094 DOI: 10.1086/368201 |
0.545 |
|
| 2003 |
Fisher SE, Lai CS, Monaco AP. Deciphering the genetic basis of speech and language disorders. Annual Review of Neuroscience. 26: 57-80. PMID 12524432 DOI: 10.1146/Annurev.Neuro.26.041002.131144 |
0.635 |
|
| 2002 |
Fisher SE, DeFries JC. Developmental dyslexia: genetic dissection of a complex cognitive trait. Nature Reviews. Neuroscience. 3: 767-80. PMID 12360321 DOI: 10.1038/Nrn936 |
0.426 |
|
| 2002 |
Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature. 418: 869-72. PMID 12192408 DOI: 10.1038/Nature01025 |
0.606 |
|
| 2002 |
Smalley SL, Kustanovich V, Minassian SL, Stone JL, Ogdie MN, McGough JJ, McCracken JT, MacPhie IL, Francks C, Fisher SE, Cantor RM, Monaco AP, Nelson SF. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American Journal of Human Genetics. 71: 959-63. PMID 12187510 DOI: 10.1086/342732 |
0.543 |
|
| 2002 |
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American Journal of Human Genetics. 70: 1183-96. PMID 11923911 DOI: 10.1086/340112 |
0.539 |
|
| 2002 |
Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP. Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric Genetics. 12: 35-41. PMID 11901358 DOI: 10.1097/00041444-200203000-00005 |
0.556 |
|
| 2002 |
Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP. FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics. 70: 1318-27. PMID 11894222 DOI: 10.1086/339931 |
0.633 |
|
| 2002 |
Newbury DF, Cleak JD, Ishikawa-Brush Y, Marlow AJ, Fisher SE, Monaco AP, Stott CM, Merricks MJ, Goodyer IM, Bolton PF, Jannoun L, Slonims V, Baird G, Pickles A, Bishop DVM, et al. A genomewide scan identifies two novel loci involved in specific language impairment American Journal of Human Genetics. 70: 384-398. PMID 11791209 DOI: 10.1086/338649 |
0.582 |
|
| 2002 |
Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP. A genomewide linkage screen for relative hand skill in sibling pairs. American Journal of Human Genetics. 70: 800-5. PMID 11774074 DOI: 10.1086/339249 |
0.509 |
|
| 2002 |
Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature Genetics. 30: 86-91. PMID 11743577 DOI: 10.1038/Ng792 |
0.578 |
|
| 2001 |
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 413: 519-23. PMID 11586359 DOI: 10.1038/35097076 |
0.631 |
|
| 2001 |
Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, Monaco AP, Stein JF, Cardon LR. Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK. Behavior Genetics. 31: 219-30. PMID 11545538 DOI: 10.1023/A:1010209629021 |
0.512 |
|
| 2001 |
Siddiqui MR, Meisner S, Tosh K, Balakrishnan K, Ghei S, Fisher SE, Golding M, Shanker Narayan NP, Sitaraman T, Sengupta U, Pitchappan R, Hill AV. A major susceptibility locus for leprosy in India maps to chromosome 10p13. Nature Genetics. 27: 439-41. PMID 11279529 DOI: 10.1038/86958 |
0.361 |
|
| 2000 |
Francks C, Fisher SE, Marlow AJ, Richardson AJ, Stein JF, Monaco AP. A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability. Prostaglandins, Leukotrienes, and Essential Fatty Acids. 63: 27-31. PMID 10970709 DOI: 10.1054/Plef.2000.0187 |
0.572 |
|
| 2000 |
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. American Journal of Human Genetics. 67: 357-68. PMID 10880297 DOI: 10.1086/303011 |
0.603 |
|
| 1999 |
Fisher SE, Stein JF, Monaco AP. A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia). European Child & Adolescent Psychiatry. 8: 47-51. PMID 10638370 DOI: 10.1007/Pl00010694 |
0.598 |
|
| 1999 |
Tanaka K, Fisher SE, Craig IW. Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis. Genomics. 58: 281-92. PMID 10373326 DOI: 10.1006/Geno.1999.5839 |
0.331 |
|
| 1999 |
Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. American Journal of Human Genetics. 64: 146-56. PMID 9915953 DOI: 10.1086/302190 |
0.536 |
|
| 1998 |
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. Localisation of a gene implicated in a severe speech and language disorder. Nature Genetics. 18: 168-70. PMID 9462748 DOI: 10.1038/Ng0298-168 |
0.629 |
|
| 1998 |
Meisner S, Siddiqui R, Fisher S, Mucklow S, Warner G, Roy S, Balakrishnan K, Pitchappan RM, Sitaraman T, Shanker NP, Narayan, Sows S, Hilll AVS. A Genome-Wide Search for Leprosy Susceptibility Genes Clinical Science. 95. DOI: 10.1042/Cs095017P |
0.318 |
|
| 1997 |
Fisher SE, Ciccodicola A, Tanaka K, Curci A, Desicato S, D'urso M, Craig IW. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp. Genomics. 45: 340-7. PMID 9344658 DOI: 10.1006/Geno.1997.4941 |
0.35 |
|
| 1996 |
Lloyd SE, Pearce SH, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SP, Wrong O, Jentsch TJ, Craig IW, Thakker RV. A common molecular basis for three inherited kidney stone diseases. Nature. 379: 445-9. PMID 8559248 DOI: 10.1038/379445A0 |
0.32 |
|
| 1995 |
Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW. Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146. Genomics. 29: 496-502. PMID 8666400 DOI: 10.1006/Geno.1995.9976 |
0.516 |
|
| 1995 |
Fisher SE, van Bakel I, Lloyd SE, Pearce SH, Thakker RV, Craig IW. Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). Genomics. 29: 598-606. PMID 8575751 DOI: 10.1006/Geno.1995.9960 |
0.335 |
|
| 1995 |
Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y. High-resolution comparative mapping of the proximal region of the mouse X chromosome. Genomics. 28: 305-10. PMID 8530041 DOI: 10.1006/Geno.1995.1146 |
0.466 |
|
| Show low-probability matches. |