| Massively parallel functional dissection of mammalian enhancers in vivo RP Patwardhan, JB Hiatt, DM Witten, MJ Kim, RP Smith, D May, C Lee, ... Nature biotechnology 30 (3), 265-270, 2012 | 685 | 2012 |
| Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice A Visel, Y Zhu, D May, V Afzal, E Gong, C Attanasio, MJ Blow, JC Cohen, ... Nature 464 (7287), 409-412, 2010 | 568 | 2010 |
| Large-scale discovery of enhancers from human heart tissue D May, MJ Blow, T Kaplan, DJ McCulley, BC Jensen, JA Akiyama, A Holt, ... Nature genetics 44 (1), 89-93, 2012 | 332 | 2012 |
| A high-resolution enhancer atlas of the developing telencephalon A Visel, L Taher, H Girgis, D May, O Golonzhka, RV Hoch, GL McKinsey, ... Cell 152 (4), 895-908, 2013 | 287 | 2013 |
| Ero1-Lα plays a key role in a HIF-1-mediated pathway to improve disulfide bond formation and VEGF secretion under hypoxia: implication for cancer D May, A Itin, O Gal, H Kalinski, E Feinstein, E Keshet Oncogene 24 (6), 1011-1020, 2005 | 225 | 2005 |
| Transgenic system for conditional induction and rescue of chronic myocardial hibernation provides insights into genomic programs of hibernation D May, D Gilon, V Djonov, A Itin, A Lazarus, O Gordon, C Rosenberger, ... Proceedings of the National Academy of Sciences 105 (1), 282-287, 2008 | 147 | 2008 |
| Functional importance of cardiac enhancer-associated noncoding RNAs in heart development and disease S Ounzain, I Pezzuto, R Micheletti, F Burdet, R Sheta, M Nemir, ... Journal of molecular and cellular cardiology 76, 55-70, 2014 | 144 | 2014 |
| 52 genetic loci influencing myocardial mass P Van der Harst, J van Setten, N Verweij, G Vogler, L Franke, ... Journal of the American College of Cardiology 68 (13), 1435-1448, 2016 | 143 | 2016 |
| Genome-wide compendium and functional assessment of in vivo heart enhancers DE Dickel, I Barozzi, Y Zhu, Y Fukuda-Yuzawa, M Osterwalder, ... Nature communications 7 (1), 12923, 2016 | 121 | 2016 |
| Chromosome 9p21 and coronary artery disease R McPherson New England Journal of Medicine 362 (18), 1736-1737, 2010 | 87 | 2010 |
| A transgenic model for conditional induction and rescue of portal hypertension reveals a role of VEGF-mediated regulation of sinusoidal fenestrations D May, V Djonov, G Zamir, M Bala, R Safadi, M Sklair-Levy, E Keshet PloS one 6 (7), e21478, 2011 | 70 | 2011 |
| Metabolic homeostasis is maintained in myocardial hibernation by adaptive changes in the transcriptome and proteome M Mayr, D May, O Gordon, B Madhu, D Gilon, X Yin, Q Xing, I Drozdov, ... Journal of Molecular and Cellular Cardiology 50 (6), 982-990, 2011 | 28 | 2011 |
| Vascular Endothelial Growth Factor–Induced Neovascularization Rescues Cardiac Function But Not Adverse Remodeling at Advanced Ischemic Heart Disease O Gordon, D Gilon, Z He, D May, A Lazarus, A Oppenheim, E Keshet Arteriosclerosis, thrombosis, and vascular biology 32 (7), 1642-1651, 2012 | 17 | 2012 |
| RNA binding protein IGF2BP2 expression is induced by stress in the heart and mediates dilated cardiomyopathy M Krumbein, F Oberman, Y Cinnamon, M Golomb, D May, G Vainer, ... Communications Biology 6 (1), 1229, 2023 | 14 | 2023 |
| Psychiatric Collaboration Models in Israel. O Avny, KC Nahum, T Michnick, T Teitelbaum, D May The Israel Medical Association Journal: IMAJ 18 (2), 71-75, 2016 | 4 | 2016 |
| Genetic testing of neurodevelopmental disorders in Israel D May, R Barshir, M Shahar, AJ Rose, D Shmueli JAMA network open 8 (8), e2527464-e2527464, 2025 | 2 | 2025 |
| Discovering predisposing genes for hereditary breast cancer using deep learning G Passi, S Lieberman, F Zahdeh, O Murik, P Renbaum, R Beeri, M Linial, ... Briefings in Bioinformatics 25 (4), 2024 | 2 | 2024 |
| Familial NSD1 Exon 3 Deletion Associated with Phenotypic and Epigenetic Variability SL Lee, A Foster, D May, C Batterton, E Ochoa, B Yngvadottir, ... Genes 16 (10), 1190, 2025 | | 2025 |
| Cytosolic PEPCK deficiency caused by a novel homozygous frame-shift variant presenting as resolved hypoglycemia and acute liver failure at birth D Burg, G Altarescu, S Korman, E Shteyer, D May Molecular Genetics and Metabolism Reports 42, 101175, 2025 | | 2025 |
| Cytosolic PEPCK deficiency caused by a novel homozygous frame-shift variant presenting as hypoglycemia and acute liver failure at birth D May, G Altarescu, S Korman, E Shteyer EUROPEAN JOURNAL OF HUMAN GENETICS 32, 168-168, 2024 | | 2024 |
Len A. PennacchioSenior Staff Scientist, Lawrence Berkeley National LaboratoryVerified email at lbl.gov
