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| 37948459 | RET enhancer haplotype-dependent remodeling of the human fetal gut development program. | PLoS Genet | 2023 |
| 37948459 | RET enhancer haplotype-dependent remodeling of the human fetal gut development program. | PLoS Genet | 2023 |
| 37585461 | <i>Ret</i> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development. | Proc Natl Acad Sci U S A | 2023 |
| 37910504 | Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure. | Cell Rep | 2023 |
| 37708408 | Cardiac muscle-restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features. | G3 (Bethesda) | 2023 |
| 37910504 | Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure. | Cell Rep | 2023 |
| 37708408 | Cardiac muscle-restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features. | G3 (Bethesda) | 2023 |
| 37585461 | <i>Ret</i> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development. | Proc Natl Acad Sci U S A | 2023 |
| 34989438 | Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores. | Genet Epidemiol | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 36508674 | Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive model. | Proc Natl Acad Sci U S A | 2022 |
| 34989438 | Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores. | Genet Epidemiol | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 36508674 | Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive model. | Proc Natl Acad Sci U S A | 2022 |
| 34285053 | Sequence-based correction of barcode bias in massively parallel reporter assays. | Genome Res | 2021 |
| 34285053 | Sequence-based correction of barcode bias in massively parallel reporter assays. | Genome Res | 2021 |
| 34006365 | Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. | J Pediatr Surg | 2021 |
| 34006365 | Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. | J Pediatr Surg | 2021 |
| 32436959 | Analysis of putative cis-regulatory elements regulating blood pressure variation. | Hum Mol Genet | 2020 |
| 32436959 | Analysis of putative cis-regulatory elements regulating blood pressure variation. | Hum Mol Genet | 2020 |
| 32839576 | The road ahead in genetics and genomics. | Nat Rev Genet | 2020 |
| 32839576 | The road ahead in genetics and genomics. | Nat Rev Genet | 2020 |
| 30262922 | Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. | Eur J Hum Genet | 2019 |
| 31666091 | Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations. | Orphanet J Rare Dis | 2019 |
| 31818953 | Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease. | Proc Natl Acad Sci U S A | 2019 |
| 30262922 | Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. | Eur J Hum Genet | 2019 |
| 31127295 | A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. | Hum Mol Genet | 2019 |
| 31068470 | Multiple <i>SCN5A</i> variant enhancers modulate its cardiac gene expression and the QT interval. | Proc Natl Acad Sci U S A | 2019 |
| 31107799 | High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease. | J Pediatr Gastroenterol Nutr | 2019 |
| 31313802 | A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease. | Hum Mol Genet | 2019 |
| 31666091 | Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations. | Orphanet J Rare Dis | 2019 |
| 31818953 | Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease. | Proc Natl Acad Sci U S A | 2019 |
| 31313802 | A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease. | Hum Mol Genet | 2019 |
| 31127295 | A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. | Hum Mol Genet | 2019 |
| 31068470 | Multiple <i>SCN5A</i> variant enhancers modulate its cardiac gene expression and the QT interval. | Proc Natl Acad Sci U S A | 2019 |
| 31107799 | High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease. | J Pediatr Gastroenterol Nutr | 2019 |
| 29261189 | RET somatic mutations are underrecognized in Hirschsprung disease. | Genet Med | 2018 |
| 30169657 | A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. | Eur Heart J | 2018 |
| 30113482 | Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. | Medicine (Baltimore) | 2018 |
| 30429575 | Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 29912962 | Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. | PLoS One | 2018 |
| 30139769 | Human cardiac <i>cis</i>-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants. | Genome Res | 2018 |
| 30044860 | The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis. | PLoS One | 2018 |
| 30224653 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 29261189 | RET somatic mutations are underrecognized in Hirschsprung disease. | Genet Med | 2018 |
| 29750786 | Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. | PLoS Genet | 2018 |
| 29379196 | Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. | Eur J Hum Genet | 2018 |
| 29509840 | MSR1 repeats modulate gene expression and affect risk of breast and prostate cancer. | Ann Oncol | 2018 |
| 29455858 | A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. | Am J Hum Genet | 2018 |
| 29677652 | Cardiomyocytes have mosaic patterns of protein expression. | Cardiovasc Pathol | 2018 |