ResearcherJohns Hopkins UniversityNo recent work listed
Erica J. Childs
Matched on OpenAlex author ID A5077977193. Sources: OpenAlex.
Their work
- Papers
- 14 (first author 2, last author 0)
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 52
2014: 1 paper · 2015: 1 paper · 2016: 3 papers · 2017: none · 2018: 1 paper · 2019: 2 papers · 2020: 2 papers · 2021: 4 papers
Papers 14
- Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. Co-author DOI 10.1001/jamaoncol.2021.3701↗
- A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. First author DOI 10.1038/s41416-021-01580-x↗
- Hepcidin-regulating iron metabolism genes and pancreatic ductal adenocarcinoma: a pathway analysis of genome-wide association studies. Co-author DOI 10.1093/ajcn/nqab217↗
- Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3. Co-author DOI 10.1158/0008-5472.can-20-3267↗
- A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer. Co-author DOI 10.1093/jnci/djz246↗
- Genome-Wide Gene-Diabetes and Gene-Obesity Interaction Scan in 8,255 Cases and 11,900 Controls from PanScan and PanC4 Consortia. Co-author DOI 10.1158/1055-9965.epi-20-0275↗
- Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer. Co-author DOI 10.1093/jnci/djy155↗
- Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. First author DOI 10.1158/1055-9965.epi-18-1235↗
- Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. Co-author DOI 10.1038/s41467-018-02942-5↗
- Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study. Co-author DOI 10.1158/1055-9965.epi-15-1217↗
- Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer. Co-author DOI 10.1158/2159-8290.cd-15-0402↗
- Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21. Co-author DOI 10.18632/oncotarget.11041↗
- Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. Co-author DOI 10.1038/ng.3341↗
- Having pancreatic cancer with tumoral loss of ATM and normal TP53 protein expression is associated with a poorer prognosis. Co-author DOI 10.1158/1078-0432.ccr-13-1239↗
Closest collaborators
The 25 strongest of 52 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Alison P. Klein · 6 shared papers, 2014–2021 · strength 0.42
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. DOI 10.1158/1055-9965.epi-18-1235↗
- Michael Goggins · 6 shared papers, 2014–2021 · strength 0.42
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. DOI 10.1158/1055-9965.epi-18-1235↗
- Kari G. Rabe · 5 shared papers, 2016–2021 · strength 0.38
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. DOI 10.1158/1055-9965.epi-18-1235↗
- Steve Gallinger · 5 shared papers, 2016–2021 · strength 0.38
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. DOI 10.1158/1055-9965.epi-18-1235↗
- Gloria M. Petersen · 5 shared papers, 2016–2021 · strength 0.38
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study. DOI 10.1158/1055-9965.epi-18-1235↗
- Ralph H. Hruban · 5 shared papers, 2014–2021 · strength 0.35
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study. DOI 10.1158/1055-9965.epi-15-1217↗
- Sapna Syngal · 4 shared papers, 2016–2021 · strength 0.31
- Paper Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene. DOI 10.1001/jamaoncol.2021.3701↗
- Paper A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO. DOI 10.1038/s41416-021-01580-x↗
- Paper Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study. DOI 10.1158/1055-9965.epi-15-1217↗
- Ayelet Borgida · 2 shared papers, 2021 · strength 0.23
- Nancy R. Porter · 2 shared papers, 2021 · strength 0.23
- Amanda L. Blackford · 2 shared papers, 2019–2021 · strength 0.18
- Nicholas Jason Roberts · 2 shared papers, 2016–2021 · strength 0.15
- George Zogopoulos · 2 shared papers, 2016–2021 · strength 0.15
- Fang‐Chi Hsu · 1 shared paper, 2021 · strength 0.11
- Giovanni Parmigiani · 1 shared paper, 2021 · strength 0.11
- Harvey A. Risch · 2 shared papers, 2016–2019 · strength 0.11
- Sara H. Olson · 2 shared papers, 2016–2019 · strength 0.10
- Robert C. Kurtz · 2 shared papers, 2016–2019 · strength 0.10
- Joseph M. Herman · 2 shared papers, 2014–2016 · strength 0.08
- Christopher Lee Wolfgang · 2 shared papers, 2014–2016 · strength 0.08
- Rachel Ε. Neale · 1 shared paper, 2019 · strength 0.07
- Paul Brennan · 1 shared paper, 2019 · strength 0.07
- Fei Chen · 1 shared paper, 2019 · strength 0.07
- Rayjean J. Hung · 1 shared paper, 2019 · strength 0.07
- Evelina Mocci · 1 shared paper, 2019 · strength 0.07
- Herbert Yu · 1 shared paper, 2019 · strength 0.07
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.