关注
David Haan
David Haan
在 ucsc.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
1879*2020
Comprehensive molecular characterization of pheochromocytoma and paraganglioma
L Fishbein, I Leshchiner, V Walter, L Danilova, AG Robertson, ...
Cancer cell 31 (2), 181-193, 2017
6732017
CDK4/6 inhibitors have potent activity in combination with pathway selective therapeutic agents in models of pancreatic cancer
J Franco, AK Witkiewicz, ES Knudsen
Oncotarget 5 (15), 6512, 2014
2352014
Pathway and network analysis of more than 2500 whole cancer genomes
MA Reyna, D Haan, M Paczkowska, LPC Verbeke, M Vazquez, ...
Nature communications 11 (1), 729, 2020
1042020
RB loss contributes to aggressive tumor phenotypes in MYC-driven triple negative breast cancer
ES Knudsen, AK McClendon, J Franco, A Ertel, P Fortina, AK Witkiewicz
Cell Cycle 14 (1), 109-122, 2015
492015
Improved genome assembly of American alligator genome reveals conserved architecture of estrogen signaling
ES Rice, S Kohno, JS John, S Pham, J Howard, LF Lareau, BL O'Connell, ...
Genome research 27 (5), 686-696, 2017
452017
Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway
J Carrot-Zhang, X Yao, S Devarakonda, A Deshpande, JS Damrauer, ...
Cell reports 34 (5), 2021
302021
A community challenge to evaluate RNA-seq, fusion detection, and isoform quantification methods for cancer discovery
A Creason, D Haan, K Dang, KE Chiotti, M Inkman, A Lamb, T Yu, Y Hu, ...
Cell systems 12 (8), 827-838. e5, 2021
232021
Epigenomic blood-based early detection of pancreatic cancer employing cell-free DNA
D Haan, A Bergamaschi, V Friedl, GD Guler, Y Ning, R Reggiardo, ...
Clinical Gastroenterology and Hepatology 21 (7), 1802-1809. e6, 2023
92023
eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants
AM Thornton, L Fang, A Lo, M McSharry, D Haan, C O’Brien, AH Berger, ...
PLOS Computational Biology 17 (7), e1009132, 2021
92021
Using transcriptional signatures to find cancer drivers with LURE
D Haan, R Tao, V Friedl, IN Anastopoulos, CK Wong, AS Weinstein, ...
PACIFIC SYMPOSIUM ON BIOCOMPUTING 2020, 343-354, 2019
72019
PCAWG Drivers and Functional Interpretation Working Group, Reimand J, Stuart JM, Raphael BJ, PCAWG Consortium
MA Reyna, D Haan, M Paczkowska, LPC Verbeke, M Vazquez, ...
Pathway and network analysis of more than 2500, 0
7
Publisher Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
I Cortés-Ciriano, JJK Lee, R Xi, D Jain, YL Jung, L Yang, D Gordenin, ...
Nature genetics 55 (5), 893-893, 2023
32023
Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
I Cortés-Ciriano, JJK Lee, R Xi, D Jain, YL Jung, L Yang, D Gordenin, ...
nature genetics 55 (6), 1076-1076, 2023
22023
Author Correction: The evolutionary history of 2,658 cancers
M Gerstung, C Jolly, I Leshchiner, SC Dentro, S Gonzalez, D Rosebrock, ...
Nature 614 (7948), E42-E42, 2023
22023
Early detection of pancreatic cancer using 5-hydroxymethylation profiles in plasma-derived cell-free DNA.
A Bergamaschi, D Haan, M Collins, G Guler, M Peters, L Gigliotti, ...
Journal of Clinical Oncology 41 (4_suppl), 672-672, 2023
22023
Validation of a Pancreatic Cancer Detection Test in New-Onset Diabetes Using Cell-Free DNA 5-Hydroxymethylation Signatures
D Haan, A Bergamaschi, GD Guler, V Friedl, Y Ning, R Reggiardo, ...
MedRxiv, 2021.12. 27.21268450, 2021
22021
Author Correction: Pan-cancer analysis of whole genomes
Nature 614 (7948), E39-E39, 2023
12023
Pancreatic cancer detection using 5-hydroxymethylation signatures in plasma-derived cell free DNA in high-risk patients with new onset diabetes.
D Haan, G Guler, A Bergamaschi, W Volkmuth, S Levy
Journal of Clinical Oncology 40 (4_suppl), 539-539, 2022
12022
Analytical Validation of an Early Detection Pancreatic Cancer Test Using 5-Hydroxymethylation Signatures
S Chowdhury, M Kesling, M Collins, V Lopez, Y Xue, G Oliveira, V Friedl, ...
The Journal of Molecular Diagnostics, 2024
2024
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