ResearcherMount Sinai HospitalNo recent work listed
Wigdan Al-Sukhni
Matched on OpenAlex author ID A5068679594. Sources: OpenAlex.
Their work
- Papers
- 3 (first author 1, last author 0)
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 15
2012: 2 papers · 2013: 1 paper
Papers 3
- Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer. First author DOI 10.1186/1479-7364-7-11↗
- Identification of germline genomic copy number variation in familial pancreatic cancer. Co-author DOI 10.1007/s00439-012-1183-1↗
- Screening for pancreatic cancer in a high-risk cohort: an eight-year experience. Co-author DOI 10.1007/s11605-011-1781-6↗
Closest collaborators
The 15 strongest of 15 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Spring Holter · 3 shared papers, 2012–2013 · strength 0.08
- Paper Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer. DOI 10.1186/1479-7364-7-11↗
- Paper Screening for pancreatic cancer in a high-risk cohort: an eight-year experience. DOI 10.1007/s11605-011-1781-6↗
- Paper Identification of germline genomic copy number variation in familial pancreatic cancer. DOI 10.1007/s00439-012-1183-1↗
- Ayelet Borgida · 3 shared papers, 2012–2013 · strength 0.08
- Paper Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer. DOI 10.1186/1479-7364-7-11↗
- Paper Screening for pancreatic cancer in a high-risk cohort: an eight-year experience. DOI 10.1007/s11605-011-1781-6↗
- Paper Identification of germline genomic copy number variation in familial pancreatic cancer. DOI 10.1007/s00439-012-1183-1↗
- Steve Gallinger · 3 shared papers, 2012–2013 · strength 0.08
- Paper Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer. DOI 10.1186/1479-7364-7-11↗
- Paper Screening for pancreatic cancer in a high-risk cohort: an eight-year experience. DOI 10.1007/s11605-011-1781-6↗
- Paper Identification of germline genomic copy number variation in familial pancreatic cancer. DOI 10.1007/s00439-012-1183-1↗
- Robert C. Grant · 2 shared papers, 2012–2013 · strength 0.06
- Zaheer S. Kanji · 1 shared paper, 2013 · strength 0.03
- Stefano Serra · 1 shared paper, 2013 · strength 0.03
- Steven Alexander Narod · 1 shared paper, 2012 · strength 0.03
- Masoom A. Haider · 1 shared paper, 2012 · strength 0.03
- Kartik S. Jhaveri · 1 shared paper, 2012 · strength 0.03
- Malcolm J. Moore · 1 shared paper, 2012 · strength 0.03
- Kari G. Rabe · 1 shared paper, 2012 · strength 0.02
- Alison P. Klein · 1 shared paper, 2012 · strength 0.02
- Sapna Syngal · 1 shared paper, 2012 · strength 0.02
- Gloria M. Petersen · 1 shared paper, 2012 · strength 0.02
- George Zogopoulos · 1 shared paper, 2012 · strength 0.02
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.