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Connection

Mohammed Orloff to Genetic Predisposition to Disease

This is a "connection" page, showing publications Mohammed Orloff has written about Genetic Predisposition to Disease.

 
Connection Strength
  
 
 
1.138
  
  1. Orloff MS, Zhang L, Bebek G, Eng C. Integrative genomic analysis reveals extended germline homozygosity with lung cancer risk in the PLCO cohort. PLoS One. 2012; 7(2):e31975.
    View in: PubMed
    Score: 0.328
  2. Carter TC, Kay DM, Pangilinan F, Almli LM, Jenkins MM, Blue EE, Sok P, White JJ, Cunniff CM, Agopian AJ, Bamshad MJ, Botto LD, Brody LC, Gucsavas-Calikoglu M, Chong JX, Gomez-Acevedo H, Lupo PJ, Moore CA, Nembhard WN, Olney RS, Olshan AF, Orloff MS, Reefhuis J, Romitti PA, Shaw GM, Werler MM, Yazdy MM, Browne ML, Howley MM. Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study. Birth Defects Res. 2025 May; 117(5):e2472.
    View in: PubMed
    Score: 0.204
  3. Patel J, Bircan E, Tang X, Orloff M, Hobbs CA, Browne ML, Botto LD, Finnell RH, Jenkins MM, Olshan A, Romitti PA, Shaw GM, Werler MM, Li J, Nembhard WN. Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach. PLoS Genet. 2021 03; 17(3):e1009413.
    View in: PubMed
    Score: 0.153
  4. Jin J, Robeson H, Fagan P, Orloff MS. Association of PARP1-specific polymorphisms and haplotypes with non-small cell lung cancer subtypes. PLoS One. 2020; 15(12):e0243509.
    View in: PubMed
    Score: 0.151
  5. Orloff MS, He X, Peterson C, Chen F, Chen JL, Mester JL, Eng C. Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes. Am J Hum Genet. 2013 Jan 10; 92(1):76-80.
    View in: PubMed
    Score: 0.087
  6. Orloff M, Peterson C, He X, Ganapathi S, Heald B, Yang YR, Bebek G, Romigh T, Song JH, Wu W, David S, Cheng Y, Meltzer SJ, Eng C. Germline mutations in MSR1, ASCC1, and CTHRC1 in patients with Barrett esophagus and esophageal adenocarcinoma. JAMA. 2011 Jul 27; 306(4):410-9.
    View in: PubMed
    Score: 0.079
  7. Waddell N, Arnold J, Cocciardi S, da Silva L, Marsh A, Riley J, Johnstone CN, Orloff M, Assie G, Eng C, Reid L, Keith P, Yan M, Fox S, Devilee P, Godwin AK, Hogervorst FB, Couch F, Grimmond S, Flanagan JM, Khanna K, Simpson PT, Lakhani SR, Chenevix-Trench G. Subtypes of familial breast tumours revealed by expression and copy number profiling. Breast Cancer Res Treat. 2010 Oct; 123(3):661-77.
    View in: PubMed
    Score: 0.070
  8. Mukherjee N, Bolin EH, Qasim A, Orloff MS, Lupo PJ, Nembhard WN. DNA methylation of the Lamin A/C gene is associated with congenital heart disease. Birth Defects Res. 2024 Jul; 116(7):e2381.
    View in: PubMed
    Score: 0.048
  9. Shiovitz S, Everett J, Huang SC, Orloff MS, Eng C, Gruber SB. Head circumference in the clinical detection of PTEN hamartoma tumor syndrome in a clinic population at high-risk of breast cancer. Breast Cancer Res Treat. 2010 Nov; 124(2):459-65.
    View in: PubMed
    Score: 0.018
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.