Marcin Imielinski
Cornell University
H-index: 57
North America-United States
Top articles of Marcin Imielinski
Title | Journal | Author(s) | Publication Date |
---|---|---|---|
Passenger mutations link cellular origins and transcriptional identity in human lung adenocarcinoma | Cancer Research | Sukanya Panja Padmaja Mantri Juan Andrade Martinez Marcin Imielinski | 2024/3/22 |
Abstract IA009: Scars of faulty DNA repair in cancer whole genomes | Cancer Research | Jeremy Setton Simon Powell Marcin Imielinski | 2024/1/9 |
Molecular evolution of classic Hodgkin lymphoma revealed through whole-genome sequencing of Hodgkin and Reed Sternberg cells | Blood cancer discovery | Francesco Maura Bachisio Ziccheddu Jenny Z Xiang Bhavneet Bhinder Joel Rosiene | 2023/5/1 |
HLA-DP on epithelial cells enables tissue damage by Nkp44+ natural killer cells in ulcerative colitis | Gastroenterology | Martin E Baumdick Annika Niehrs Frauke Degenhardt Maria Schwerk Ole Hinrichs | 2023/10/1 |
A mass balance principle for finding loose ends in cancer genomes | Nature Genetics | Zi-Ning Choo Marcin Imieliński | 2023/12 |
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes | Nature | Esther Rheinbay Morten Muhlig Nielsen Federico Abascal Jeremiah A Wala Ofer Shapira | 2020/2/6 |
Patterns of somatic structural variation in human cancer genomes (vol 578, pg 112, 2020) | Nature | Yilong Li Nicola D Roberts Jeremiah A Wala Ofer Shapira Steven E Schumacher | 2020/2/6 |
Long-molecule scars of backup DNA repair in BRCA1-and BRCA2-deficient cancers | Nature | Jeremy Setton Kevin Hadi Zi-Ning Choo Katherine S Kuchin Huasong Tian | 2023/9/7 |
Most large structural variants in cancer genomes can be detected without long reads | Nature Genetics | Zi-Ning Choo Julie M Behr Aditya Deshpande Kevin Hadi Xiaotong Yao | 2023/12 |
Detecting significantly recurrent genomic connections from simple and complex rearrangements in the cancer genome | bioRxiv | Shu Zhang Kiran H Kumar Ofer Shapira Xiaotong Yao Jeremiah Wala | 2023 |
Author Correction: Pan-cancer analysis of whole genomes | Nature | 2023/2/16 | |
Faster detection of somatic structural variants | Nature Biomedical Engineering | Zi-Ning Choo Marcin Imieliński | 2023/7 |
The importance of escalating molecular diagnostics in patients with low-grade pediatric brain cancer | Molecular Case Studies | Majd Al Assaad Gunes Gundem Benjamin Liechty Andrea Sboner Juan Medina | 2023/12/1 |
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes | Nature | Esther Rheinbay Morten Muhlig Nielsen Federico Abascal Jeremiah A Wala Ofer Shapira | 2023/2/16 |
Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing | Nature genetics | Isidro Cortés-Ciriano Jake June-Koo Lee Ruibin Xi Dhawal Jain Youngsook L Jung | 2023/6 |
Genomic sequence context differs between germline and somatic structural variants allowing for their differentiation in tumor samples without paired normals | bioRxiv | Wolu Chukwu Siyun Lee Alexander Crane Shu Zhang Ipsa Mittra | 2023/10/12 |
Author Correction: Patterns of somatic structural variation in human cancer genomes | Nature | Yilong Li Nicola D Roberts Jeremiah A Wala Ofer Shapira Steven E Schumacher | 2023/2/16 |
Publisher Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing | Nature genetics | Isidro Cortés-Ciriano Jake June-Koo Lee Ruibin Xi Dhawal Jain Youngsook L Jung | 2023/5 |
A sequence context-based germline filter for structural variant calling from tumor samples without paired normal | W Chukwu S Lee A Crane S Zhang I Mittra | 2023/10/12 | |
Author Correction: The evolutionary history of 2,658 cancers | Nature | Moritz Gerstung Clemency Jolly Ignaty Leshchiner Stefan C Dentro Santiago Gonzalez | 2023/2/16 |