| Year |
Citation |
Score |
| 2023 |
Li Y, Wen J, Li G, Chen J, Sun Q, Liu W, Guan W, Lai B, Szatkiewicz J, He X, Sullivan P. DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network. Research Square. PMID 36824788 DOI: 10.21203/rs.3.rs-2399024/v1 |
0.314 |
|
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Szatkiewicz JP, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.308 |
|
| 2021 |
Halvorsen M, Szatkiewicz J, Mudgal P, Yu D, Nordsletten AE, Mataix-Cols D, Mathews CA, Scharf JM, Mattheisen M, Robertson MM, McQuillin A, Crowley JJ. Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. Molecular Psychiatry. PMID 34526668 DOI: 10.1038/s41380-021-01277-w |
0.318 |
|
| 2020 |
Harner MK, Lichtenstein M, Farrell M, Dietterich TE, Filmyer DM, Bruno LM, Biondi TF, Crowley JJ, Lázaro-Muñoz G, Stowe R, Shaughnessy RA, Berg JS, Szatkiewicz J, Sullivan PF, Josiassen RC. Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome. Schizophrenia Research. PMID 32943312 DOI: 10.1016/J.Schres.2020.08.012 |
0.332 |
|
| 2020 |
Brucker A, Lu W, Marceau West R, Yu QY, Hsiao CK, Hsiao TH, Lin CH, Magnusson PKE, Sullivan PF, Szatkiewicz JP, Lu TP, Tzeng JY. Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis. Plos Computational Biology. 16: e1007797. PMID 32365089 DOI: 10.1371/Journal.Pcbi.1007797 |
0.449 |
|
| 2020 |
Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, ... ... Szatkiewicz JP, et al. Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature Communications. 11: 1842. PMID 32296054 DOI: 10.1038/S41467-020-15707-W |
0.392 |
|
| 2020 |
Farrell M, Lichtenstein M, Harner MK, Crowley JJ, Filmyer DM, Lázaro-Muñoz G, Dietterich TE, Bruno LM, Shaughnessy RA, Biondi TF, Burkholder S, Donmoyer J, Berg JS, Szatkiewicz J, Sullivan PF, et al. Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature. Translational Psychiatry. 10: 42. PMID 32066678 DOI: 10.1038/S41398-020-0725-X |
0.323 |
|
| 2020 |
Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, ... ... Szatkiewicz JP, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology. e12880. PMID 32064741 DOI: 10.1111/Adb.12880 |
0.364 |
|
| 2019 |
Szatkiewicz JP, Fromer M, Nonneman RJ, Ancalade N, Johnson JS, Stahl EA, Rees E, Bergen SE, Hultman CM, Kirov G, O'Donovan M, Owen M, Holmans P, Sklar P, Sullivan PF, et al. Characterization of Single Gene Copy Number Variants in Schizophrenia. Biological Psychiatry. PMID 31767120 DOI: 10.1016/J.Biopsych.2019.09.023 |
0.378 |
|
| 2019 |
Szatkiewicz J, Crowley JJ, Adolfsson AN, Åberg KA, Alaerts M, Genovese G, McCarroll S, Del-Favero J, Adolfsson R, Sullivan PF. The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. Translational Psychiatry. 9: 60. PMID 30718465 DOI: 10.1038/S41398-019-0414-9 |
0.407 |
|
| 2019 |
Farrell M, Lichtenstein M, Crowley J, Filmyer D, Lázaro-Muñoz G, Shaughnessy R, Mackenzie IR, Hirsch-Reinshagen V, Stowe R, Evans J, Berg J, Szatkiewicz J, Josiassen R, Sullivan PF. THE GENOMICS OF HIGHLY TREATMENT RESISTANT SCHIZOPHRENIA European Neuropsychopharmacology. 29: S1006-S1007. DOI: 10.1016/J.Euroneuro.2017.08.401 |
0.42 |
|
| 2019 |
McQuillin A, Halvorsen M, Mattheisen M, Robertson M, Curtis D, Gurling H, Mudgal P, Szatkiewicz J, Sullivan P, Crowley J. Identifying Susceptibility Loci For Tourette'S Syndrome In A Densely Affected Pedigree European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.066 |
0.434 |
|
| 2018 |
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Common-variant associations with fragile X syndrome. Molecular Psychiatry. PMID 30531935 DOI: 10.1038/S41380-018-0290-3 |
0.39 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Szatkiewicz JP, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.367 |
|
| 2018 |
Wang W, Sun W, Wang W, Szatkiewicz J. A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection. Bmc Bioinformatics. 19: 74. PMID 29490610 DOI: 10.1186/S12859-018-2077-6 |
0.366 |
|
| 2017 |
Xia K, Zhang J, Ahn M, Jha S, Crowley JJ, Szatkiewicz J, Li T, Zou F, Zhu H, Hibar D, Thompson P, Sullivan PF, Styner M, Gilmore JH, et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. Translational Psychiatry. 7: e1188. PMID 28763065 DOI: 10.1038/Tp.2017.159 |
0.397 |
|
| 2017 |
Yilmaz Z, Szatkiewicz JP, Crowley JJ, Ancalade N, Brandys MK, van Elburg A, de Kovel CG, Adan RA, Hinney A, Hebebrand J, Gratacos M, Fernandez-Aranda F, Escaramis G, Gonzalez JR, Estivill X, et al. Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa. Psychiatric Genetics. PMID 28368970 DOI: 10.1097/Ypg.0000000000000172 |
0.431 |
|
| 2016 |
Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NM, Blumenthal I, Chiang C, Ota V, Hultman C, O'Dushlaine C, et al. Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics. Part A. PMID 27759917 DOI: 10.1002/Ajmg.A.38021 |
0.366 |
|
| 2016 |
Magnusson PK, Lee D, Chen X, Szatkiewicz J, Pramana S, Teo S, Sullivan PF, Feuk L, Pawitan Y. One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-7. PMID 26899349 DOI: 10.1017/Thg.2016.5 |
0.39 |
|
| 2015 |
Tzeng JY, Magnusson PK, Sullivan PF, Szatkiewicz JP. A New Method for Detecting Associations with Rare Copy-Number Variants. Plos Genetics. 11: e1005403. PMID 26431523 DOI: 10.1371/Journal.Pgen.1005403 |
0.426 |
|
| 2015 |
Wang W, Wang W, Sun W, Crowley JJ, Szatkiewicz JP. Allele-specific copy-number discovery from whole-genome and whole-exome sequencing. Nucleic Acids Research. PMID 25883151 DOI: 10.1093/Nar/Gkv319 |
0.383 |
|
| 2014 |
Goldstein JI, Jarskog LF, Hilliard C, Alfirevic A, Duncan L, Fourches D, Huang H, Lek M, Neale BM, Ripke S, Shianna K, Szatkiewicz JP, Tropsha A, van den Oord EJ, Cascorbi I, et al. Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. Nature Communications. 5: 4757. PMID 25187353 DOI: 10.1038/Ncomms5757 |
0.358 |
|
| 2014 |
Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, et al. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry. 19: 762-73. PMID 24776740 DOI: 10.1038/Mp.2014.40 |
0.459 |
|
| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, ... ... Szatkiewicz J, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.391 |
|
| 2014 |
Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, et al. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry. 19: 37-40. PMID 24217254 DOI: 10.1038/Mp.2013.156 |
0.364 |
|
| 2014 |
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics. 23: 1669-76. PMID 24163246 DOI: 10.1093/Hmg/Ddt540 |
0.409 |
|
| 2013 |
Szatkiewicz JP, Neale BM, O'Dushlaine C, Fromer M, Goldstein JI, Moran JL, Chambert K, Kähler A, Magnusson PK, Hultman CM, Sklar P, Purcell S, McCarroll SA, Sullivan PF. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample. Molecular Psychiatry. 18: 1178-84. PMID 23938935 DOI: 10.1038/Mp.2013.98 |
0.449 |
|
| 2013 |
Szatkiewicz JP, Wang W, Sullivan PF, Wang W, Sun W. Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentation. Nucleic Acids Research. 41: 1519-32. PMID 23275535 DOI: 10.1093/Nar/Gks1363 |
0.333 |
|
| 2013 |
Collins AL, Kim Y, Szatkiewicz JP, Bloom RJ, Hilliard CE, Quackenbush CR, Meier S, Rivas F, Mayoral F, Cichon S, Nöthen MM, Rietschel M, Sullivan PF. Identifying bipolar disorder susceptibility loci in a densely affected pedigree. Molecular Psychiatry. 18: 1245-6. PMID 23247078 DOI: 10.1038/Mp.2012.176 |
0.442 |
|
| 2012 |
Crowley JJ, Kim Y, Szatkiewicz JP, Pratt AL, Quackenbush CR, Adkins DE, van den Oord E, Bogue MA, Yang H, Wang W, Threadgill DW, de Villena FP, McLeod HL, Sullivan PF. Genome-wide association mapping of loci for antipsychotic-induced extrapyramidal symptoms in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 322-35. PMID 22207321 DOI: 10.1007/S00335-011-9385-8 |
0.395 |
|
| 2011 |
Root TL, Szatkiewicz JP, Jonassaint CR, Thornton LM, Pinheiro AP, Strober M, Bloss C, Berrettini W, Schork NJ, Kaye WH, Bergen AW, Magistretti P, Brandt H, Crawford S, Crow S, et al. Association of candidate genes with phenotypic traits relevant to anorexia nervosa. European Eating Disorders Review : the Journal of the Eating Disorders Association. 19: 487-93. PMID 21780254 DOI: 10.1002/Erv.1138 |
0.408 |
|
| 2011 |
Jonassaint CR, Szatkiewicz JP, Bulik CM, Thornton LM, Bloss C, Berrettini WH, Kaye WH, Bergen AW, Magistretti P, Strober M, Keel PK, Brandt H, Crawford S, Crow S, Fichter MM, et al. Absence of association between specific common variants of the obesity-related FTO gene and psychological and behavioral eating disorder phenotypes. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 454-61. PMID 21438147 DOI: 10.1002/Ajmg.B.31182 |
0.37 |
|
| 2010 |
Billings T, Sargent EE, Szatkiewicz JP, Leahy N, Kwak IY, Bektassova N, Walker M, Hassold T, Graber JH, Broman KW, Petkov PM. Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping. Plos One. 5: e15340. PMID 21170346 DOI: 10.1371/Journal.Pone.0015340 |
0.329 |
|
| 2010 |
Hutchins LN, Ding Y, Szatkiewicz JP, Von Smith R, Yang H, de Villena FPM, Churchill GA, Graber JH. CGDSNPdb: a database resource for error-checked and imputed mouse SNPs. Database : the Journal of Biological Databases and Curation. 2010: baq008. PMID 20624716 DOI: 10.1093/Database/Baq008 |
0.354 |
|
| 2010 |
Leme AS, Berndt A, Williams LK, Tsaih SW, Szatkiewicz JP, Verdugo R, Paigen B, Shapiro SD. A survey of airway responsiveness in 36 inbred mouse strains facilitates gene mapping studies and identification of quantitative trait loci. Molecular Genetics and Genomics : Mgg. 283: 317-26. PMID 20143096 DOI: 10.1007/S00438-010-0515-X |
0.337 |
|
| 2009 |
Casselbrant ML, Mandel EM, Jung J, Ferrell RE, Tekely K, Szatkiewicz JP, Ray A, Weeks DE. Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. Bmc Medical Genetics. 10: 85. PMID 19728873 DOI: 10.1186/1471-2350-10-85 |
0.362 |
|
| 2009 |
Yang H, Ding Y, Hutchins LN, Szatkiewicz J, Bell TA, Paigen BJ, Graber JH, de Villena FPM, Churchill GA. A customized and versatile high-density genotyping array for the mouse Nature Methods. 6: 663-666. PMID 19668205 DOI: 10.1038/Nmeth.1359 |
0.391 |
|
| 2008 |
Paigen K, Szatkiewicz JP, Sawyer K, Leahy N, Parvanov ED, Ng SH, Graber JH, Broman KW, Petkov PM. The recombinational anatomy of a mouse chromosome. Plos Genetics. 4: e1000119. PMID 18617997 DOI: 10.1371/Journal.Pgen.1000119 |
0.311 |
|
| 2008 |
Su Z, Tsaih SW, Szatkiewicz J, Shen Y, Paigen B. Candidate genes for plasma triglyceride, FFA, and glucose revealed from an intercross between inbred mouse strains NZB/B1NJ and NZW/LacJ. Journal of Lipid Research. 49: 1500-10. PMID 18362393 DOI: 10.1194/Jlr.M800053-Jlr200 |
0.356 |
|
| 2008 |
Szatkiewicz JP, Beane GL, Ding Y, Hutchins L, Pardo-Manuel De Villena F, Churchill GA. An imputed genotype resource for the laboratory mouse Mammalian Genome. 19: 199-208. PMID 18301946 DOI: 10.1007/S00335-008-9098-9 |
0.336 |
|
| 2005 |
Szatkiewicz JP, Feingold E. QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies. Genetic Epidemiology. 28: 326-40. PMID 15662636 DOI: 10.1002/Gepi.20065 |
0.52 |
|
| 2004 |
Szatkiewicz JP, Feingold E. A powerful and robust new linkage statistic for discordant sibling pairs. American Journal of Human Genetics. 75: 906-9. PMID 15368196 DOI: 10.1086/425523 |
0.516 |
|
| 2003 |
T Cuenco K, Szatkiewicz JP, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for selected sibling pairs. American Journal of Human Genetics. 73: 863-73. PMID 12970847 DOI: 10.1086/378589 |
0.538 |
|
| 2003 |
Szatkiewicz JP, T Cuenco K, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs. American Journal of Human Genetics. 73: 874-85. PMID 12970846 DOI: 10.1086/378590 |
0.504 |
|
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