| Year |
Citation |
Score |
| 2018 |
Manley W, Moreau MP, Azaro M, Siecinski SK, Davis G, Buyske S, Vieland V, Bassett AS, Brzustowicz L. Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype. Plos One. 13: e0194233. PMID 29529098 DOI: 10.1371/Journal.Pone.0194233 |
0.423 |
|
| 2016 |
Bruni M, Flax JF, Buyske S, Shindhelm AD, Witton C, Brzustowicz LM, Bartlett CW. Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds. Behavior Genetics. PMID 27826669 DOI: 10.1007/S10519-016-9821-3 |
0.325 |
|
| 2016 |
Hernandez K, Swiatkowski P, Patel MV, Liang C, Dudzinski NR, Brzustowicz LM, Firestein BL. Overexpression of Isoforms of Nitric Oxide Synthase 1 Adaptor Protein, Encoded by a Risk Gene for Schizophrenia, Alters Actin Dynamics and Synaptic Function. Frontiers in Cellular Neuroscience. 10: 6. PMID 26869880 DOI: 10.3389/Fncel.2016.00006 |
0.347 |
|
| 2015 |
Carrel D, Hernandez K, Kwon M, Mau C, Trivedi MP, Brzustowicz LM, Firestein BL. Nitric oxide synthase 1 adaptor protein, a protein implicated in schizophrenia, controls radial migration of cortical neurons. Biological Psychiatry. 77: 969-78. PMID 25542305 DOI: 10.1016/J.Biopsych.2014.10.016 |
0.34 |
|
| 2014 |
Merico D, Costain G, Butcher NJ, Warnica W, Ogura L, Alfred SE, Brzustowicz LM, Bassett AS. MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Frontiers in Neurology. 5: 238. PMID 25484875 DOI: 10.3389/Fneur.2014.00238 |
0.401 |
|
| 2014 |
Vieland VJ, Walters KA, Azaro M, Brzustowicz LM, Lehner T. The value of regenotyping older linkage data sets with denser marker panels. Human Heredity. 78: 9-16. PMID 24969307 DOI: 10.1159/000360003 |
0.339 |
|
| 2014 |
Choi J, Ababon MR, Soliman M, Lin Y, Brzustowicz LM, Matteson PG, Millonig JH. Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum. Plos One. 9: e87208. PMID 24520327 DOI: 10.1371/Journal.Pone.0087208 |
0.33 |
|
| 2014 |
Walters KA, Huang Y, Azaro M, Tobin K, Lehner T, Brzustowicz LM, Vieland VJ. Meta-analysis of repository data: impact of data regularization on NIMH schizophrenia linkage results. Plos One. 9: e84696. PMID 24454738 DOI: 10.1371/Journal.Pone.0084696 |
0.338 |
|
| 2014 |
Vieland VJ, Walters KA, Lehner T, Azaro M, Tobin K, Huang Y, Brzustowicz LM. Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies. The American Journal of Psychiatry. 171: 350-9. PMID 24170318 DOI: 10.1176/Appi.Ajp.2013.11121766 |
0.435 |
|
| 2014 |
Bartlett CW, Hou L, Flax JF, Hare A, Cheong SY, Fermano Z, Zimmerman-Bier B, Cartwright C, Azaro MA, Buyske S, Brzustowicz LM. A genome scan for loci shared by autism spectrum disorder and language impairment. The American Journal of Psychiatry. 171: 72-81. PMID 24170272 DOI: 10.1176/Appi.Ajp.2013.12081103 |
0.351 |
|
| 2014 |
Merico D, Costain G, Butcher N, Warnica W, Ogura L, Alfred SE, Brzustowicz L, Bassett AS. MicroRNA target genes and risk for schizophrenia in 22q11.2 deletion syndrome Frontiers in Neurology. 5. DOI: 10.3389/Fneur.2014.00221 |
0.389 |
|
| 2013 |
Lionel AC, Vaags AK, Sato D, Gazzellone MJ, Mitchell EB, Chen HY, Costain G, Walker S, Egger G, Thiruvahindrapuram B, Merico D, Prasad A, Anagnostou E, Fombonne E, Zwaigenbaum L, ... ... Brzustowicz LM, et al. Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Human Molecular Genetics. 22: 2055-66. PMID 23393157 DOI: 10.1093/Hmg/Ddt056 |
0.396 |
|
| 2012 |
Brzustowicz LM, Bassett AS. miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome. Frontiers in Genetics. 3: 291. PMID 23248646 DOI: 10.3389/Fgene.2012.00291 |
0.399 |
|
| 2012 |
Bartlett CW, Flax JF, Fermano Z, Hare A, Hou L, Petrill SA, Buyske S, Brzustowicz LM. Gene × gene interaction in shared etiology of autism and specific language impairment. Biological Psychiatry. 72: 692-9. PMID 22704665 DOI: 10.1016/J.Biopsych.2012.05.019 |
0.366 |
|
| 2012 |
Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophrenia Research. 137: 166-8. PMID 22381191 DOI: 10.1016/J.Schres.2012.02.009 |
0.42 |
|
| 2011 |
Brzustowicz L, Freedman R. Digging more deeply for genetic effects in psychiatric illness. The American Journal of Psychiatry. 168: 1017-20. PMID 21969044 DOI: 10.1176/Appi.Ajp.2011.11060928 |
0.325 |
|
| 2011 |
Hou L, Phillips C, Azaro M, Brzustowicz LM, Bartlett CW. Validation of a cost-efficient multi-purpose SNP panel for disease based research. Plos One. 6: e19699. PMID 21611176 DOI: 10.1371/Journal.Pone.0019699 |
0.334 |
|
| 2011 |
Moreau MP, Bruse SE, David-Rus R, Buyske S, Brzustowicz LM. Altered microRNA expression profiles in postmortem brain samples from individuals with schizophrenia and bipolar disorder. Biological Psychiatry. 69: 188-93. PMID 21183010 DOI: 10.1016/J.Biopsych.2010.09.039 |
0.315 |
|
| 2010 |
Flax JF, Hare A, Azaro MA, Vieland VJ, Brzustowicz LM. Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci. Journal of Neurodevelopmental Disorders. 2: 210-223. PMID 21125004 DOI: 10.1007/S11689-010-9063-2 |
0.399 |
|
| 2010 |
Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families. Human Heredity. 70: 232-44. PMID 20948219 DOI: 10.1159/000320367 |
0.373 |
|
| 2010 |
Costain G, Ho A, Crawley AP, Mikulis DJ, Brzustowicz LM, Chow EW, Bassett AS. Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report. Schizophrenia Research. 122: 81-4. PMID 20638248 DOI: 10.1016/J.Schres.2010.06.014 |
0.445 |
|
| 2010 |
Hadzimichalis NM, Previtera ML, Moreau MP, Li B, Lee GH, Dulencin AM, Matteson PG, Buyske S, Millonig JH, Brzustowicz LM, Firestein BL. NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia. Schizophrenia Research. 124: 248-50. PMID 20605702 DOI: 10.1016/J.Schres.2010.05.009 |
0.37 |
|
| 2010 |
Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophrenia Research. 121: 187-92. PMID 20541371 DOI: 10.1016/J.Schres.2010.05.021 |
0.418 |
|
| 2010 |
Bassett AS, Scherer SW, Brzustowicz LM. Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease. The American Journal of Psychiatry. 167: 899-914. PMID 20439386 DOI: 10.1176/Appi.Ajp.2009.09071016 |
0.443 |
|
| 2009 |
Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH. Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2. Biological Psychiatry. 66: 911-7. PMID 19615670 DOI: 10.1016/J.Biopsych.2009.05.027 |
0.349 |
|
| 2009 |
Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, ... ... Brzustowicz LM, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135 |
0.409 |
|
| 2009 |
Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM. Identification of a schizophrenia-associated functional noncoding variant in NOS1AP. The American Journal of Psychiatry. 166: 434-41. PMID 19255043 DOI: 10.1176/Appi.Ajp.2008.08081266 |
0.409 |
|
| 2009 |
Kremeyer B, García J, Kymäläinen H, Wratten N, Restrepo G, Palacio C, Miranda AL, López C, Restrepo M, Bedoya G, Brzustowicz LM, Ospina-Duque J, Arbeláez MP, Ruiz-Linares A. Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. Human Heredity. 67: 163-73. PMID 19077434 DOI: 10.1159/000181154 |
0.443 |
|
| 2008 |
Brzustowicz LM, Bassett AS. Phenotype matters: the case for careful characterization of relevant traits. The American Journal of Psychiatry. 165: 1096-8. PMID 18765489 DOI: 10.1176/Appi.Ajp.2008.08060897 |
0.465 |
|
| 2008 |
Brzustowicz LM. NOS1AP in schizophrenia. Current Psychiatry Reports. 10: 158-63. PMID 18474209 DOI: 10.1007/S11920-008-0027-0 |
0.427 |
|
| 2007 |
Saviouk V, Moreau MP, Tereshchenko IV, Brzustowicz LM. Association of synapsin 2 with schizophrenia in families of Northern European ancestry. Schizophrenia Research. 96: 100-11. PMID 17766091 DOI: 10.1016/J.Schres.2007.07.031 |
0.439 |
|
| 2006 |
Logue MW, Brzustowicz LM, Bassett AS, Chow EW, Vieland VJ. A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17. Human Heredity. 62: 47-54. PMID 17019084 DOI: 10.1159/000096035 |
0.407 |
|
| 2006 |
Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry. 60: 152-62. PMID 16631129 DOI: 10.1016/J.Biopsych.2006.02.015 |
0.398 |
|
| 2005 |
Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, Dicicco-Bloom E, Brzustowicz LM, Millonig JH. Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. American Journal of Human Genetics. 77: 851-68. PMID 16252243 DOI: 10.1086/497705 |
0.389 |
|
| 2005 |
Xu B, Wratten N, Charych EI, Buyske S, Firestein BL, Brzustowicz LM. Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder. Plos Medicine. 2: e263. PMID 16146415 DOI: 10.1371/Journal.Pmed.0020263 |
0.451 |
|
| 2005 |
Bartlett CW, Gharani N, Millonig JH, Brzustowicz LM. Three autism candidate genes: a synthesis of human genetic analysis with other disciplines. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 23: 221-34. PMID 15749247 DOI: 10.1016/J.Ijdevneu.2004.10.004 |
0.35 |
|
| 2005 |
Saviouk V, Chow EW, Bassett AS, Brzustowicz LM. Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44. Molecular Psychiatry. 10: 375-83. PMID 15340354 DOI: 10.1038/Sj.Mp.4001582 |
0.476 |
|
| 2004 |
Wassink TH, Brzustowicz LM, Bartlett CW, Szatmari P. The search for autism disease genes. Mental Retardation and Developmental Disabilities Research Reviews. 10: 272-83. PMID 15666342 DOI: 10.1002/Mrdd.20041 |
0.358 |
|
| 2004 |
Bartlett CW, Flax JF, Logue MW, Smith BJ, Vieland VJ, Tallal P, Brzustowicz LM. Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment. Human Heredity. 57: 10-20. PMID 15133308 DOI: 10.1159/000077385 |
0.376 |
|
| 2004 |
Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. American Journal of Human Genetics. 74: 1057-63. PMID 15065015 DOI: 10.1086/420774 |
0.465 |
|
| 2004 |
Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH. Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder Molecular Psychiatry. 9: 474-484. PMID 15024396 DOI: 10.1038/Sj.Mp.4001498 |
0.319 |
|
| 2003 |
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics. 73: 34-48. PMID 12802786 DOI: 10.1086/376549 |
0.416 |
|
| 2002 |
Brzustowicz LM, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS. Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22. Human Heredity. 54: 199-209. PMID 12771552 DOI: 10.1159/000070665 |
0.457 |
|
| 2002 |
Bassett AS, Chow EW, Vieland VJ, Brzustowicz L. Is schizophrenia linked to chromosome 1q? Science (New York, N.Y.). 298: 2277; author reply 2. PMID 12494945 DOI: 10.1126/Science.1076508 |
0.308 |
|
| 2002 |
Bassett AS, Chow EW, Weksberg R, Brzustowicz L. Schizophrenia and genetics: new insights. Current Psychiatry Reports. 4: 307-14. PMID 12126600 DOI: 10.1007/S11920-996-0051-X |
0.445 |
|
| 2002 |
Bartlett CW, Flax JF, Logue MW, Vieland VJ, Bassett AS, Tallal P, Brzustowicz LM. A major susceptibility locus for specific language impairment is located on 13q21. American Journal of Human Genetics. 71: 45-55. PMID 12048648 DOI: 10.1086/341095 |
0.353 |
|
| 2002 |
Waterwort DM, Bassett AS, Brzustowicz LM. Recent advances in the genetics of schizophrenia. Cellular and Molecular Life Sciences : Cmls. 59: 331-48. PMID 11915947 DOI: 10.1007/S00018-002-8426-6 |
0.457 |
|
| 2001 |
Bassett AS, Chow EW, O'Neill S, Brzustowicz LM. Genetic insights into the neurodevelopmental hypothesis of schizophrenia. Schizophrenia Bulletin. 27: 417-30. PMID 11596844 DOI: 10.1093/Oxfordjournals.Schbul.A006884 |
0.418 |
|
| 2001 |
Bassett AS, Chow EW, Waterworth DM, Brzustowicz L. Genetic insights into schizophrenia. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 131-7. PMID 11280081 DOI: 10.1177/070674370104600203 |
0.444 |
|
| 2001 |
Hodgkinson KA, Murphy J, O'Neill S, Brzustowicz L, Bassett AS. Genetic counselling for schizophrenia in the era of molecular genetics. Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. 46: 123-30. PMID 11280080 DOI: 10.1177/070674370104600202 |
0.405 |
|
| 2000 |
Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS. Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science (New York, N.Y.). 288: 678-82. PMID 10784452 DOI: 10.1126/Science.288.5466.678 |
0.467 |
|
| 1999 |
Brzustowicz LM, Honer WG, Chow EW, Little D, Hogan J, Hodgkinson K, Bassett AS. Linkage of familial schizophrenia to chromosome 13q32. American Journal of Human Genetics. 65: 1096-103. PMID 10486329 DOI: 10.1086/302579 |
0.438 |
|
| 1999 |
Brzustowicz LM, Farrell S, Khan MB, Weksberg R. Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome American Journal of Human Genetics. 65: 779-783. PMID 10441586 DOI: 10.1086/302527 |
0.352 |
|
| 1997 |
Brzustowicz LM, Honer WG, Chow EW, Hogan J, Hodgkinson K, Bassett AS. Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p. American Journal of Human Genetics. 61: 1388-96. PMID 9399881 DOI: 10.1086/301623 |
0.331 |
|
| 1997 |
Bassett A, Honer W, Chow E, McAlduff J, Hodgkinson K, Kirkham S, Brzustowicz L. A susceptibility locus for schizophrenia on chromosome 6 using positive symptom scores as quantitative traits Schizophrenia Research. 24: 50. DOI: 10.1016/S0920-9964(97)82143-3 |
0.396 |
|
| 1993 |
Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC. Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B. Genomics. 15: 365-71. PMID 8449502 DOI: 10.1006/Geno.1993.1069 |
0.357 |
|
| 1993 |
Kleyn PW, Wang CH, Lien LL, Vitale E, Pan J, Ross BM, Grunn A, Palmer DA, Warburton D, Brzustowicz LM. Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region. Proceedings of the National Academy of Sciences of the United States of America. 90: 6801-5. PMID 8341701 DOI: 10.1073/Pnas.90.14.6801 |
0.352 |
|
| 1993 |
Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, Ross B, Romano DM, Parano E, Pavone L, Brzustowicz LM. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nature Genetics. 5: 344-50. PMID 8298641 DOI: 10.1038/Ng1293-344 |
0.321 |
|
| 1993 |
Petrukhin K, Fischer SG, Pirastu M, Tanzi RE, Chernov I, Devoto M, Brzustowicz LM, Cayanis E, Vitale E, Russo JJ. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nature Genetics. 5: 338-43. PMID 8298640 DOI: 10.1038/Ng1293-338 |
0.359 |
|
| 1990 |
Weeks DE, Brzustowicz L, Squires-Wheeler E, Cornblatt B, Lehner T, Stefanovich M, Bassett A, Gilliam TC, Ott J, Erlenmeyer-Kimling L. Report of a workshop on genetic linkage studies in schizophrenia. Schizophrenia Bulletin. 16: 673-86. PMID 2077644 DOI: 10.1093/Schbul/16.4.673 |
0.417 |
|
| Show low-probability matches. |