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Year | Number of Results |
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2010 | 1 |
2021 | 2 |
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Page 1
A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease.
Genome Res. 2021 Dec;31(12):2199-2208. doi: 10.1101/gr.275667.121. Epub 2021 Nov 15.
Genome Res. 2021.
PMID: 34782358
Free PMC article.
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Padhi EM, Hayeck TJ, Cheng Z, Chatterjee S, Mannion BJ, Byrska-Bishop M, Willems M, Pinson L, Redon S, Benech C, Uguen K, Audebert-Bellanger S, Le Marechal C, Férec C, Efthymiou S, Rahman F, Maqbool S, Maroofian R, Houlden H, Musunuri R, Narzisi G, Abhyankar A, Hunter RD, Akiyama J, Fries LE, Ng JK, Mehinovic E, Stong N, Allen AS, Dickel DE, Bernier RA, Gorkin DU, Pennacchio LA, Zody MC, Turner TN.
Padhi EM, et al. Among authors: fries le.
Hum Genomics. 2021 Jul 13;15(1):44. doi: 10.1186/s40246-021-00342-3.
Hum Genomics. 2021.
PMID: 34256850
Free PMC article.
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RET enhancer haplotype-dependent remodeling of the human fetal gut development program.
Chatterjee S, Fries LE, Yaacov O, Hu N, Berk-Rauch HE, Chakravarti A.
Chatterjee S, et al. Among authors: fries le.
PLoS Genet. 2023 Nov 10;19(11):e1011030. doi: 10.1371/journal.pgen.1011030. eCollection 2023 Nov.
PLoS Genet. 2023.
PMID: 37948459
Free PMC article.
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Racial/Ethnic group differences in bipolar symptomatology in a community sample of persons with bipolar I disorder.
Perron BE, Fries LE, Kilbourne AM, Vaughn MG, Bauer MS.
Perron BE, et al. Among authors: fries le.
J Nerv Ment Dis. 2010 Jan;198(1):16-21. doi: 10.1097/NMD.0b013e3181c818c5.
J Nerv Ment Dis. 2010.
PMID: 20061864
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