Publication Overview
Journal Article (90)
1.
Journal Article
115 (51), pp. 13021 - 13026 (2018)
Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 2.
Journal Article
34 (6), pp. 996 - 1011 (2018)
Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell 3.
Journal Article
23 (6), pp. 900 - 904 (2018)
Esrrb Unlocks Silenced Enhancers for Reprogramming to Naive Pluripotency - Correction. Cell Stem Cell 4.
Journal Article
25 (10), e7, pp. 2676 - 2688 (2018)
tRNA Translocation by the Eukaryotic 80S Ribosome and the Impact of GTP Hydrolysis. Cell Reports 5.
Journal Article
177 (8), pp. 691 - 699 (2018)
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Am J Med Genet B Neuropsychiatr Genet 6.
Journal Article
33, pp. 20 - 24 (2018)
Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. Stem Cell Research 7.
Journal Article
210 (4), pp. 1527 - 1542 (2018)
Identification of two novel candidate genes for insulin secretion by comparative genomics of multiple backcross populations. Genetics 8.
Journal Article
33, pp. 120 - 124 (2018)
Generation of two human isogenic iPSC lines from fetal dermal fibroblasts. Stem Cell Research 9.
Journal Article
7, e40757 (2018)
Targets and genomic constraints of ectopic Dnmt3b expression. eLife 10.
Journal Article
145 (22), pii: dev168617 (2018)
Comparative genomic analysis of embryonic, lineage-converted and stem cell-derived motor neurons. Development 11.
Journal Article
563 (7731), p. 325 (2018)
Paying PIs from grants blocks talent and diversity. Nature 12.
Journal Article
16 (1), 138 (2018)
Classifying human promoters by occupancy patterns identifies recurring sequence elements, combinatorial binding, and spatial interactions. BMC Biology 13.
Journal Article
14 (11), e1007793 (2018)
Synthetic STARR-seq reveals how DNA shape and sequence modulate transcriptional output and noise. PLoS Genetics 14.
Journal Article
10 (466), eaau7137 (2018)
Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand. Science Translational Medicine 15.
Journal Article
20, pp. 1481 - 1482 (2018)
Response to Peron et al. GENETICS IN MEDICINE 16.
Journal Article
103 (5), pp. 512 - 521 (2018)
Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis. Calcified Tissue International 17.
Journal Article
9, 9:484 (2018)
Network and Pathway Analysis of Toxicogenomics Data. Frontiers in Genetics 18.
Journal Article
8 (1), 14611 (2018)
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation. Scientific Reports 19.
Journal Article
50 (10), pp. 1442 - 1451 (2018)
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature Genetics 20.
Journal Article
50 (10), pp. 1463 - 1473 (2018)
Dynamic 3D chromatin architecture determines enhancer specificity and morphogenetic identity in limb development. Nature Genetics