Kelly Lammerts van Bueren

Author

University of California, San Francisco

Also Known As

Kelly Lammerts Van Bueren, Kelly Lammerts van Bueren

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

University of California, San Francisco Lawrence Berkeley National Laboratory University College London The University of Queensland University of California, Merced

About

Kelly Lammerts van Bueren is an author at University of California, San Francisco specializing in medicine, gene expression, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	459
2	Cell Biology	5	5	387
3	Natural Sciences	2	2	72
4	Cellular Physiology	2	2	163
5	Molecular Biology	1	1	10

Kelly Lammerts van Bueren

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants Stephen C.J. Parker, Michael L. Stitzel, D. Leland Taylor, Proceedings of the National Academy of Sciences	2013	730
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating<i>Gbx2</i>expression in the pharyngeal ectoderm Amélie Calmont, Sarah Ivins, Kelly Lammerts van Bueren, Development Pharyngeal EctodermPaa AbnormalitiesCellular PhysiologyPaa DevelopmentTissue Development	2009	144
Pax9 and Jagged1 act downstream of Gli3 in vertebrate limb development Edwina McGlinn, Kelly Lammerts van Bueren, Salvatore Fiorenza, Mechanisms of Development Cell LineageDevelopmental BiologyDevelopmental GeneticsGeneticsGenomic Mechanism	2005	99
Cardiovascular development and survival require Mef2c function in the myocardial but not the endothelial lineage Stefan C. Materna, Tanvi Sinha, Ralston M. Barnes, Developmental Biology Developmental BiologyCardiac ReprogrammingCardiovascular DiseaseMef2c FunctionPhysiology	2018	63
Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome Kelly Lammerts van Bueren, Irinna Papangeli, Francesca Rochais, Developmental Biology GeneticsMolecular GeneticsDeletion SyndromeTranscriptional RegulationTbx1 Null Cells	2010	62
Noncoding deletions reveal a gene that is critical for intestinal function Danit Oz-Levi, Tsviya Olender, Ifat Bar-Joseph, Nature Systems BiologyIntestinal FunctionGeneticsGenomic MechanismGene Characterization	2019	39
<i>HIC2</i> Is a Novel Dosage-Dependent Regulator of Cardiac Development Located Within the Distal 22q11 Deletion Syndrome Region Iain M. Dykes, Kelly Lammerts van Bueren, Rebekah J. Ashmore, Circulation Research	2014	34
Differential Etv2 threshold requirement for endothelial and erythropoietic development Tanvi Sinha, Kelly Lammerts van Bueren, Diane E. Dickel, Cell Reports	2022	24
Evolutionary conservation and murine embryonic expression of the gene encoding the SERTA domain-containing protein CDCA4 (HEPP) Jennifer S. Bennetts, Lindsay Fowles, Jennifer Berkman, Gene Developmental BiologyProtein ExpressionGeneticsGene StructureGene Regulation	2006	23
HIC2 regulates isoform switching during maturation of the cardiovascular system Iain M. Dykes, Kelly Lammerts van Bueren, Peter Scambler Journal of Molecular and Cellular Cardiology Cardiac MuscleCardiac Progenitor CellsCreatine KinaseCardiovascular FunctionCongenital Heart Anomaly	2017	19

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