| 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 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Flax J, Gwin C, Wilson S, Fradkin Y, Buyske S, Brzustowicz L. Social (Pragmatic) Communication Disorder: Another name for the Broad Autism Phenotype? Autism : the International Journal of Research and Practice. 1362361318822503. PMID 30931583 DOI: 10.1177/1362361318822503 |
0.29 |
|
| 2006 |
Widom CS, Brzustowicz LM. MAOA and the "cycle of violence:" childhood abuse and neglect, MAOA genotype, and risk for violent and antisocial behavior. Biological Psychiatry. 60: 684-9. PMID 16814261 DOI: 10.1016/J.Biopsych.2006.03.039 |
0.289 |
|
| 2004 |
Gharani N, Benayed R, Mancuso V, Brzustowicz L, Millonig J. Erratum: Association of the homeobox transcription factor, ENGRAILED 2, with autism spectrum disorder (Molecular Psychiatry (2004) 9 (474-484) DOI:10.1038/sj.mp.4001498) Molecular Psychiatry. 9. DOI: 10.1038/Sj.Mp.4001515 |
0.283 |
|
| 2020 |
Widom CS, Miller D, Li X, Gordon D, Brzustowicz L. Childhood maltreatment, serotonin transporter gene, and risk for callous and unemotional traits: A prospective investigation. Psychiatry Research. 291: 113271. PMID 32629297 DOI: 10.1016/J.Psychres.2020.113271 |
0.283 |
|
| 2018 |
Williams M, Prem S, Zhou X, Matteson P, Yeung PL, Lu CW, Pang Z, Brzustowicz L, Millonig JH, Dicicco-Bloom E. Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells (NPCs). Journal of Visualized Experiments : Jove. PMID 29553565 DOI: 10.3791/56628 |
0.281 |
|
| 2019 |
Hare-Harris AE, Mitchel MW, Myers SM, Mitchel AD, King BR, Ruocco BG, Martin CL, Flax JF, Brzustowicz LM. Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index. Journal of Neurodevelopmental Disorders. 11: 21. PMID 31519145 DOI: 10.1186/S11689-019-9283-Z |
0.28 |
|
| 2023 |
Alibutud R, Hansali S, Cao X, Zhou A, Mahaganapathy V, Azaro M, Gwin C, Wilson S, Buyske S, Bartlett CW, Flax JF, Brzustowicz LM, Xing J. Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments. International Journal of Molecular Sciences. 24. PMID 37686052 DOI: 10.3390/ijms241713248 |
0.279 |
|
| 2011 |
Logan J, Petrill SA, Flax J, Justice LM, Hou L, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment. Behavior Genetics. 41: 651-9. PMID 21193955 DOI: 10.1007/S10519-010-9435-0 |
0.276 |
|
| 2018 |
Svane KC, Asis EK, Omelchenko A, Kunnath AJ, Brzustowicz LM, Silverstein SM, Firestein BL. d-Serine administration affects nitric oxide synthase 1 adaptor protein and DISC1 expression in sex-specific manner. Molecular and Cellular Neurosciences. PMID 29601869 DOI: 10.1016/J.Mcn.2018.03.011 |
0.258 |
|
| 2017 |
Fradkin Y, Flax J, Gwinn C, Wilson S, Law K, Brzustowicz L. 85.3 Emotional Regulation in Children With Autism Spectrum Disorder With and Without Structural Language Impairment Journal of the American Academy of Child and Adolescent Psychiatry. 56. DOI: 10.1016/J.Jaac.2017.07.494 |
0.254 |
|
| 1994 |
Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 21: 27-33. PMID 8088801 DOI: 10.1006/Geno.1994.1220 |
0.25 |
|
| 2012 |
Nikulina V, Widom CS, Brzustowicz LM. Child abuse and neglect, MAOA, and mental health outcomes: a prospective examination. Biological Psychiatry. 71: 350-7. PMID 22030358 DOI: 10.1016/J.Biopsych.2011.09.008 |
0.25 |
|
| 2008 |
Bruse SE, Moreau MP, Azaro MA, Zimmerman R, Brzustowicz LM. Improvements to bead-based oligonucleotide ligation SNP genotyping assays Biotechniques. 45: 559-571. PMID 19007340 DOI: 10.2144/000112960 |
0.245 |
|
| 1995 |
Brzustowicz LM, Wang CH, Matseoane D, Kleyn PW, Vitale E, Das K, Penchaszadeh GK, Munsat TL, Hausmanowa-Petrusewicz I, Gilliam TC. Linkage disequilibrium and haplotype analysis among Polish families with Spinal Muscular Atrophy American Journal of Human Genetics. 56: 210-215. PMID 7825580 |
0.245 |
|
| 1990 |
Munsat TL, Skerry L, Korf B, Pober B, Schapira Y, Gascon GG, Al-Rajeh SM, Dubowitz V, Davies K, Brzustowicz LM, Penchaszadeh GK, Gilliam TC. Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q) Neurology. 40: 1831-1836. PMID 2247230 DOI: 10.1212/WNL.40.12.1831 |
0.244 |
|
| 1994 |
Brzustowicz LM, Allitto BA, Matseoane D, Theve R, Michaud L, Chatkupt S, Sugarman E, Penchaszadeh GK, Suslak L, Koenigsberger MR, Gilliam TC, Handelin BL. Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy American Journal of Human Genetics. 54: 482-488. PMID 8116617 |
0.24 |
|
| 2016 |
Fradkin Y, Flax J, Majmundar P, Wilson S, Gwin C, Brzustowicz L. 5.20 Diagnosing Social Pragmatic Communication Disorder And Gender Differences Journal of the American Academy of Child and Adolescent Psychiatry. 55. DOI: 10.1016/J.Jaac.2016.09.279 |
0.236 |
|
| 2007 |
Brzustowicz LM. Size matters: the unexpected challenge of detecting linkage in large cohorts. The American Journal of Psychiatry. 164: 192-4. PMID 17267776 DOI: 10.1176/Ajp.2007.164.2.192 |
0.231 |
|
| 1997 |
Scott WK, Speer MC, Leal SM, Brzustowicz LM, Haynes CS, Pericak-Vance MA. False positive rates in a genomic screen for complex quantitative traits. Genetic Epidemiology. 14: 891-6. PMID 9433596 DOI: 10.1002/(Sici)1098-2272(1997)14:6<891::Aid-Gepi55>3.0.Co;2-H |
0.229 |
|
| 1994 |
Wang CH, Kleyn PW, Xu J, Vitale E, Carter TA, Ross BM, Das K, Soares MB, Brzustowicz LM, Kunkel LM, Conrad Gilliam T. Isolation of coding sequences and evaluation of candidate genes for spinal muscular atrophy Pediatric Neurology. 11: 101. DOI: 10.1016/0887-8994(94)90206-2 |
0.224 |
|
| 2013 |
Moreau MP, Bruse SE, Jornsten R, Liu Y, Brzustowicz LM. Chronological changes in microRNA expression in the developing human brain. Plos One. 8: e60480. PMID 23613727 DOI: 10.1371/Journal.Pone.0060480 |
0.223 |
|
| 1995 |
Wang CH, Kleyn PW, Vitale E, Ross BM, Lien L, Xu J, Carter TA, Brzustowicz LM, Obici S, Selig S. Refinement of the spinal muscular atrophy locus by genetic and physical mapping. American Journal of Human Genetics. 56: 202-9. PMID 7825579 |
0.222 |
|
| 2009 |
Freedman R, Lewis DA, Michels R, Pine DS, Schultz SK, Tamminga CA, Andreasen NC, Brady KT, Brent DA, Brzustowicz L, Carter CS, Eisenberg L, Goldman H, Javitt DC, Leibenluft E, et al. Conflict of interest-- an issue for every psychiatrist. The American Journal of Psychiatry. 166: 274. PMID 19255048 DOI: 10.1176/Appi.Ajp.2009.09010093 |
0.222 |
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| 1992 |
Brzustowicz LM, Kleyn PW, Boyce FM, Lien LL, Monaco AP, Penchaszadeh GK, Das K, Wang CH, Munsat TL, Ott J, Kunkel LM, Gilliam TC. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6 Genomics. 13: 991-998. PMID 1505990 DOI: 10.1016/0888-7543(92)90012-H |
0.22 |
|
| 2015 |
Widom CS, Horan J, Brzustowicz L. Childhood maltreatment predicts allostatic load in adulthood. Child Abuse & Neglect. PMID 25700779 DOI: 10.1016/J.Chiabu.2015.01.016 |
0.219 |
|
| 2009 |
Carrel D, Du Y, Komlos D, Hadzimichalis NM, Kwon M, Wang B, Brzustowicz LM, Firestein BL. NOS1AP regulates dendrite patterning of hippocampal neurons through a carboxypeptidase E-mediated pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 8248-58. PMID 19553464 DOI: 10.1523/Jneurosci.5287-08.2009 |
0.218 |
|
| 2019 |
Fradkin Y, Flax J, Gwin C, Brzustowicz L. 33.4 Emotional Regulation In Children With Asd With And Without Concurrent Language Impairment Journal of the American Academy of Child and Adolescent Psychiatry. 58. DOI: 10.1016/J.Jaac.2019.07.842 |
0.218 |
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| 2022 |
Zhou A, Cao X, Mahaganapathy V, Azaro M, Gwin C, Wilson S, Buyske S, Bartlett CW, Flax JF, Brzustowicz LM, Xing J. Common genetic risk factors in ASD and ADHD co-occurring families. Human Genetics. PMID 36251081 DOI: 10.1007/s00439-022-02496-z |
0.215 |
|
| 1993 |
Brzustowicz LM, Merette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TC. Assessment of nonallelic genetic heterogeneity of chronic (Type II and III) spinal muscular atrophy Human Heredity. 43: 380-387. PMID 7904586 DOI: 10.1159/000154164 |
0.214 |
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| 2022 |
Wong A, Zhou A, Cao X, Mahaganapathy V, Azaro M, Gwin C, Wilson S, Buyske S, Bartlett CW, Flax JF, Brzustowicz LM, Xing J. MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders. Genes. 13. PMID 35893067 DOI: 10.3390/genes13081329 |
0.214 |
|
| 1990 |
Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, Dubowitz V, Zerres K, Hausmanowa-Petrusewicz I, Ott J, Munsat TL, et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2-13.3 Nature. 344: 540-541. PMID 2320125 DOI: 10.1038/344540A0 |
0.213 |
|
| 2019 |
Ruocco B, Mayani R, Sharma S, Wilson S, Vahi K, Voinea S, Davis G, Valentine-Cooper W, Mathew J, Arens Y, Deelman E, Azaro M, Vieland V, Ambite JL, Brzustowicz L. M15 Enhancing Access To Data At The National Institute Of Health Repository And Genomics Resource European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.115 |
0.209 |
|
| 1990 |
Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, Dubowitz V, Munsat TL, Ott J, Davies KE. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy Nature. 345: 823-825. PMID 1972783 DOI: 10.1038/345823A0 |
0.205 |
|
| 2001 |
Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, et al. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation. Molecular Psychiatry. 6: 259-60. PMID 11326292 DOI: 10.1038/Sj.Mp.4000128 |
0.203 |
|
| 1997 |
Brzustowicz LM, Gardner JP, Hopp L, Jeanclos E, Ott J, Yang XY, Fekete Z, Aviv A. Linkage analysis using platelet-activating factor Ca2+ response in transformed lymphoblasts. Hypertension. 29: 158-64. PMID 9039096 DOI: 10.1161/01.Hyp.29.1.158 |
0.197 |
|
| 2020 |
Crosta CM, Hernandez K, Bhattiprolu AK, Fu AY, Moore JC, Clarke SG, Dudzinski NR, Brzustowicz LM, Paradiso KG, Firestein BL. Characterization hiPSC-derived neural progenitor cells and neurons to investigate the role of NOS1AP isoforms in human neuron dendritogenesis. Molecular and Cellular Neurosciences. 103562. PMID 32987141 DOI: 10.1016/j.mcn.2020.103562 |
0.19 |
|
| 2010 |
Ott J, Wang X, Elston RC, Zhu X, Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, ... ... Brzustowicz LM, et al. Subject Index Vol. 70, 2010 Human Heredity. 70: 303-303. DOI: 10.1159/000324573 |
0.187 |
|
| 2002 |
Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... Brzustowicz LM, et al. Subject Index Vol. 54, 2002 Human Heredity. 54: 220. DOI: 10.1159/000071494 |
0.187 |
|
| 1998 |
Brzustowicz LM. Molecular genetic approaches to the study of language Human Biology. 70: 325-345. PMID 9549242 |
0.181 |
|
| 2015 |
Brzustowicz LM, Moreau MP, Bruse SE, David-Rus R, Buyske S. Reply to: Reproducibility and Visual Inspection of Data. Biological Psychiatry. PMID 26774966 DOI: 10.1016/J.Biopsych.2015.11.011 |
0.176 |
|
| 2011 |
Ott J, Wang X, Elston RC, Zhu X, Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, ... ... Brzustowicz LM, et al. Contents Vol. 70, 2010 Human Heredity. 70. DOI: 10.1159/000324574 |
0.176 |
|
| 2002 |
Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... Brzustowicz LM, et al. Contents Vol. 54, 2002 Human Heredity. 54: 221. DOI: 10.1159/000071492 |
0.176 |
|
| 2003 |
Dempfle A, Hinney A, Hebebrand J, Schäfer H, Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG, Malley JD, Naiman DQ, Bailey-Wilson JE, Nothnagel M, Fürst R, Rohde K, ... Brzustowicz LM, et al. Tribute to Lodewijk Sandkuijl Human Heredity. 54: 165. DOI: 10.1159/000071490 |
0.172 |
|
| 1991 |
Kleyn PW, Brzustowicz LM, Wilhelmsen KA, Freimer NB, Miller JM, Munsat TL, Gilliam TC. Spinal muscular atrophy is not the result of mutations at the beta–hexosaminidase or GM<inf>2</inf>–activator locus Neurology. 41: 1418-1422. PMID 1679910 |
0.165 |
|
| 2023 |
Petrill SA, Klamer BG, Buyske S, Willcutt EG, Gruen JR, Francis DJ, Flax JF, Brzustowicz LM, Bartlett CW. The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait. Genes. 14. PMID 37761888 DOI: 10.3390/genes14091748 |
0.162 |
|
| 1991 |
Lien LL, Boyce FM, Kleyn P, Brzustowicz LM, Menninger J, Ward DC, Gilliam TC, Kunkel LM. Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13 Proceedings of the National Academy of Sciences of the United States of America. 88: 7873-7876. PMID 1881920 DOI: 10.1073/PNAS.88.17.7873 |
0.156 |
|
| 2003 |
Flax JF, Realpe-Bonilla T, Hirsch LS, Brzustowicz LM, Bartlett CW, Tallal P. Specific language impairment in families: evidence for co-occurrence with reading impairments. Journal of Speech, Language, and Hearing Research : Jslhr. 46: 530-43. PMID 14696984 DOI: 10.1044/1092-4388(2003/043) |
0.155 |
|
| 1997 |
Brzustowicz LM, Allitto BA. Clinical molecular genetic testing Journal of the American Medical Women's Association (1972). 52: 11-15. PMID 1997109216 |
0.155 |
|
| 2001 |
Tallal P, Hirsch LS, Realpe-Bonilla T, Miller S, Brzustowicz LM, Bartlett C, Flax JF. Familial aggregation in specific language impairment. Journal of Speech, Language, and Hearing Research : Jslhr. 44: 1172-82. PMID 11708534 DOI: 10.1044/1092-4388(2001/091) |
0.154 |
|
| 2022 |
Connacher R, Williams M, Prem S, Yeung PL, Matteson P, Mehta M, Markov A, Peng C, Zhou X, McDermott CR, Pang ZP, Flax J, Brzustowicz L, Lu CW, Millonig JH, et al. Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses. Stem Cell Reports. PMID 35623351 DOI: 10.1016/j.stemcr.2022.04.019 |
0.152 |
|
| 1993 |
Brzustowicz LM, Mérette C, Xie X, Townsend L, Gilliam TC, Ott J. Molecular and statistical approaches to the detection and correction of errors in genotype databases. American Journal of Human Genetics. 53: 1137-45. PMID 8213837 |
0.15 |
|
| 1993 |
Bernard LE, McPherson JD, Wasmuth JJ, Kreklywich CN, Brzustowicz LM, Wood S. Linkage mapping detects two secondary microdeletions in cell hybrid HHW1064, used to isolate DNA probes from within 5q11.2→q13.3 Cytogenetic and Genome Research. 64: 46-48. PMID 8508678 DOI: 10.1159/000133558 |
0.146 |
|
| 1991 |
Brzustowicz LM, Wilhelmsen KC, Gilliam TC. Genetic analysis of childhood-onset spinal muscular atrophy Advances in Neurology. 56: 181-187. PMID 1853756 |
0.138 |
|
| 2022 |
Connacher R, Williams M, Prem S, Yeung PL, Matteson P, Mehta M, Markov A, Peng C, Zhou X, McDermott CR, Pang ZP, Flax J, Brzustowicz L, Lu CW, Millonig JH, et al. Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses. Stem Cell Reports. 17: 1786. PMID 35830838 DOI: 10.1016/j.stemcr.2022.06.007 |
0.137 |
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