Connection

Co-Authors

This is a "connection" page, showing publications co-authored by RICHARD GIBBS and MARIE-CLAUDE GINGRAS.
Connection Strength

3.037
  1. Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplant. Life Sci Alliance. 2021 09; 4(9).
    View in: PubMed
    Score: 0.722
  2. Double Mosaicism in Xia-Gibbs Syndrome. Am J Med Genet A. 2026 Feb 25.
    View in: PubMed
    Score: 0.248
  3. Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism. Hum Mutat. 2022 12; 43(12):2033-2053.
    View in: PubMed
    Score: 0.196
  4. Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications. Genet Med. 2021 12; 23(12):2404-2414.
    View in: PubMed
    Score: 0.181
  5. Germline mutation in POLR2A: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulation. HGG Adv. 2021 Jan 14; 2(1).
    View in: PubMed
    Score: 0.172
  6. Community-based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability. Mol Genet Genomic Med. 2020 10; 8(10):e1439.
    View in: PubMed
    Score: 0.169
  7. An open access pilot freely sharing cancer genomic data from participants in Texas. Sci Data. 2016 Feb 16; 3:160010.
    View in: PubMed
    Score: 0.124
  8. Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation. Cell Rep. 2016 Feb 02; 14(4):907-919.
    View in: PubMed
    Score: 0.123
  9. Whole-genome sequencing for optimized patient management. Sci Transl Med. 2011 Jun 15; 3(87):87re3.
    View in: PubMed
    Score: 0.090
  10. Association between somatostatin receptor 5 gene polymorphisms and pancreatic cancer risk and survival. Cancer. 2011 Jul 01; 117(13):2863-72.
    View in: PubMed
    Score: 0.087
  11. Sequencing the full-length of the phosphatase and tensin homolog (PTEN) gene in hepatocellular carcinoma (HCC) using the 454 GS20 and Illumina GA DNA sequencing platforms. World J Surg. 2009 Apr; 33(4):647-52.
    View in: PubMed
    Score: 0.077
  12. Expanding the Clinical and Molecular Spectrum of TUBB2B Through Distinct Variants Identified Across Multiple Families. medRxiv. 2025 Dec 29.
    View in: PubMed
    Score: 0.061
  13. Pre-sequencing assessment of RNA-Seq library quality using real-time qPCR. Biotechniques. 2025 Sep-Oct; 77(9-10):319-329.
    View in: PubMed
    Score: 0.061
  14. The GENESTAR manual for biospecimen collection biobanking and omics data generation from commercial space missions. NPJ Microgravity. 2025 May 14; 11(1):16.
    View in: PubMed
    Score: 0.059
  15. An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports KAT6B as a novel neuroblastoma susceptibility gene. Genet Med Open. 2025; 3:101901.
    View in: PubMed
    Score: 0.057
  16. Somatic mutations of esophageal adenocarcinoma: a comparison between Black and White patients. Sci Rep. 2024 04 18; 14(1):8988.
    View in: PubMed
    Score: 0.055
  17. Novel potential ALL low-risk markers revealed by gene expression profiling with new high-throughput SSH-CCS-PCR. Leukemia. 2003 Sep; 17(9):1891-900.
    View in: PubMed
    Score: 0.052
  18. Structural variation across 138,134 samples in the TOPMed consortium. Res Sq. 2023 Feb 03.
    View in: PubMed
    Score: 0.050
  19. Structural variation across 138,134 samples in the TOPMed consortium. bioRxiv. 2023 Jan 25.
    View in: PubMed
    Score: 0.050
  20. Transmission event of SARS-CoV-2 delta variant reveals multiple vaccine breakthrough infections. BMC Med. 2021 10 01; 19(1):255.
    View in: PubMed
    Score: 0.046
  21. Transmission event of SARS-CoV-2 Delta variant reveals multiple vaccine breakthrough infections. medRxiv. 2021 Jul 12.
    View in: PubMed
    Score: 0.045
  22. DNA methylation patterns identify subgroups of pancreatic neuroendocrine tumors with clinical association. Commun Biol. 2021 02 03; 4(1):155.
    View in: PubMed
    Score: 0.044
  23. Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases. Hum Mutat. 2020 12; 41(12):2094-2104.
    View in: PubMed
    Score: 0.043
  24. NF-?B and STAT3 co-operation enhances high glucose induced aggressiveness of cholangiocarcinoma cells. Life Sci. 2020 Dec 01; 262:118548.
    View in: PubMed
    Score: 0.043
  25. Whole-genome landscape of pancreatic neuroendocrine tumours. Nature. 2017 03 02; 543(7643):65-71.
    View in: PubMed
    Score: 0.033
  26. Genomic analyses identify molecular subtypes of pancreatic cancer. Nature. 2016 Mar 03; 531(7592):47-52.
    View in: PubMed
    Score: 0.031
  27. Trans-ancestry mutational landscape of hepatocellular carcinoma genomes. Nat Genet. 2014 Dec; 46(12):1267-73.
    View in: PubMed
    Score: 0.028
  28. Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature. 2012 Nov 15; 491(7424):399-405.
    View in: PubMed
    Score: 0.025
  29. Genomic sequencing of key genes in mouse pancreatic cancer cells. Curr Mol Med. 2012 Mar; 12(3):331-41.
    View in: PubMed
    Score: 0.024
  30. Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome. Am J Hum Genet. 2012 Feb 10; 90(2):282-9.
    View in: PubMed
    Score: 0.023
  31. Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma. HPB (Oxford). 2009 Aug; 11(5):435-44.
    View in: PubMed
    Score: 0.020
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.