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Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Hum Genomics. 2021 Jul 13;15(1):44. doi: 10.1186/s40246-021-00342-3.
Hum Genomics. 2021.
PMID: 34256850
Free PMC article.
A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease.
Chatterjee S, Karasaki KM, Fries LE, Kapoor A, Chakravarti A.
Chatterjee S, et al. Among authors: fries le.
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.
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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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