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Jae Woong Sull 3 Articles
Differential Parental Transmission of Markers in BCL3 among Korean Cleft Case-parent Trios.
Beyoung Yun Park, Jae Woong Sull, Jung Yong Park, Sun Ha Jee, Terri H Beaty
J Prev Med Public Health. 2009;42(1):1-4.
DOI: https://doi.org/10.3961/jpmph.2009.42.1.1
  • 4,706 View
  • 48 Download
  • 14 Crossref
AbstractAbstract PDF
OBJECTIVES
Isolated cleft lip with or without cleft palate (CL/P) is among the most common human birth defects, with a prevalence of approximately 1 in 700 live births. The B-Cell Leukemia/lymphoma 3 (BCL3) gene has been suggested as a candidate gene for CL/P based on association and linkage studies in some populations. This study tests for an association between markers in BCL3 and isolated, non-syndromic CL/P using a case-parent trio design, while considering parent-of-origin effects. METHODS: Forty case-parent trios were genotyped for two single nucleotide polymorphisms (SNPs) in the BCL3 gene. We performed a transmission disequilibrium test (TDT) on individual SNPs, and the FAMHAP package was used to estimate haplotype frequencies and to test for excess transmission of multi-SNP haplotypes. RESULTS: The odds ratio for transmission of the minor allele, OR (transmission), was significant for SNP rs8100239 (OR=3.50, p=0.004) and rs2965169 (OR=2.08, p=0.027) when parent-of-origin was not considered. Parent-specific TDT revealed that SNP rs8100239 showed excess maternal transmission. Analysis of haplotypes of rs2965169 and rs8100239 also suggested excess maternal transmission. CONCLUSIONS: BCL3 appears to influence risk of CL/P through a parent-of-origin effect with excess maternal transmission.
Summary

Citations

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  • Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)
    Lord J. J. Gowans, Carissa L. Comnick, Peter A. Mossey, Mekonen A. Eshete, Wasiu L. Adeyemo, Thirona Naicker, Waheed A. Awotoye, Aline Petrin, Chinyere Adeleke, Peter Donkor, Tamara D. Busch, Olutayo James, Mobolanle O. Ogunlewe, Mary Li, Joy Olotu, Mohan
    The Cleft Palate-Craniofacial Journal.2022; 59(7): 841.     CrossRef
  • Association of nucleotide variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 genes with nonsyndromic cleft lip with/without cleft palate in multigenerational families: A retrospective study
    PraveenKumar Neela, SrinivasReddy Gosla, Akhter Husain, Vasavi Mohan, Sravya Thumoju, BV Rajeshwari
    Contemporary Clinical Dentistry.2021; 12(2): 138.     CrossRef
  • Genetic Factors in Nonsyndromic Orofacial Clefts
    Mahamad Irfanulla Khan, Prashanth CS, Narasimha Murthy Srinath
    Global Medical Genetics.2020; 07(04): 101.     CrossRef
  • An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis
    Giovanna Marchetti, Domenico Girelli, Carlotta Zerbinati, Barbara Lunghi, Simonetta Friso, Silvia Meneghetti, Matteo Coen, Teresa Gagliano, Giuseppe Guastella, Marie-Luce Bochaton-Piallat, Francesca Pizzolo, Francesco Mascoli, Giovanni Malerba, Matteo Bov
    Thrombosis and Haemostasis.2015; 113(03): 655.     CrossRef
  • Genomic expression in non syndromic cleft lip and palate patients: A review
    D. Mehrotra
    Journal of Oral Biology and Craniofacial Research.2015; 5(2): 86.     CrossRef
  • Variant of BCL3 gene is strongly associated with five-year survival of non-small-cell lung cancer patients
    Foteinos-Ioannis D. Dimitrakopoulos, Anna G. Antonacopoulou, Anastasia Kottorou, Stella Marousi, Ioulia Koukourikou, Melpomeni Kalofonou, Nikolaos Panagopoulos, Chrisoula Scopa, Dimitrios Dougenis, Helen Papadaki, Athanasios G. Papavassiliou, Haralabos P.
    Lung Cancer.2015; 89(3): 311.     CrossRef
  • Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians
    Jane C. Figueiredo, Stephanie Ly, Haley Raimondi, Kathy Magee, James W. Baurley, Pedro A. Sanchez‐Lara, Ugonna Ihenacho, Caroline Yao, Christopher K. Edlund, David van den Berg, Graham Casey, Yves A. DeClerk, Jonathan M. Samet, William Magee
    American Journal of Medical Genetics Part A.2014; 164(10): 2572.     CrossRef
  • Genome‐wide approaches (GWA) in oral and craniofacial diseases research
    H Kim, S Gordon, R Dionne
    Oral Diseases.2013; 19(2): 111.     CrossRef
  • Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease
    Anne-Sophie Jannot, Jeanne Amiel, Anna Pelet, Francesca Lantieri, Raquel M Fernandez, Joke B G M Verheij, Merce Garcia-Barcelo, Stacey Arnold, Isabella Ceccherini, Salud Borrego, Robert M W Hofstra, Paul K H Tam, Arnold Munnich, Aravinda Chakravarti, Fran
    European Journal of Human Genetics.2012; 20(9): 917.     CrossRef
  • Gene Expression Changes in C57BL/6J and DBA/2J Mice Following Prenatal Alcohol Exposure
    Chris Downing, Stephen Flink, Maria L. Florez‐McClure, Thomas E. Johnson, Boris Tabakoff, Katerina J. Kechris
    Alcoholism: Clinical and Experimental Research.2012; 36(9): 1519.     CrossRef
  • BCL3 gene role in facial morphology
    Baiba Lace, Inga Kempa, Janis Klovins, Janis Stavusis, Astrida Krumina, Ilze Akota, Biruta Barkane, Alexandre R. Vieira, Erika Nagle, Ieva Grinfelde, Ieva Maulina
    Birth Defects Research Part A: Clinical and Molecular Teratology.2012; 94(11): 918.     CrossRef
  • Microdeletion of Chromosome 15q24.3–25.2 and Orofacial Clefting
    Bindya Sing, Dongli Song, Glenn Desandre, Balaji Govindaswami, Scott Rosenthal, Shelly Gunn, Robert Wallerstein
    The Cleft Palate-Craniofacial Journal.2011; 48(5): 596.     CrossRef
  • MTHFR and MSX1 contribute to the risk of nonsyndromic cleft lip/palate
    Triin Jagomägi, Tiit Nikopensius, Kaarel Krjutškov, Veronika Tammekivi, Triin Viltrop, Mare Saag, Andres Metspalu
    European Journal of Oral Sciences.2010; 118(3): 213.     CrossRef
  • Parent‐of‐origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/palate
    José Suazo, José Luis Santos, Lilian Jara, Rafael Blanco
    American Journal of Medical Genetics Part A.2010; 152A(8): 2011.     CrossRef
Association between Alcohol Drinking and Cardiovascular Disease Mortality and All-cause Mortality: Kangwha Cohort Study.
Sang Wook Yi, Sang Hyun Yoo, Jae Woong Sull, Heechoul Ohrr
J Prev Med Public Health. 2004;37(2):120-126.
  • 2,455 View
  • 113 Download
AbstractAbstract PDF
OBJECTIONS: This study sought to examine relationships between alcohol drinking and cardiovascular disease mortality and all-cause mortality. METHODS: From March 1985 through December 1999, 2, 696 males and 3, 595 females aged 55 or over as of 1985 were followed up for their mortality until 31 December 1999. We calculated the mortality risk ratios by level of alcohol consumption. Among the drinker, the level of alcohol consumption was calculated by the frequency of alcohol comsumption and the type of alcohol. Cox proportional hazard model was used to adjust for confounding factors. RESULTS: Among males, compared to abstainer, heavy drinker had significantly higher mortality in all cause (Risk ratio=1.35), cardiovascular disease (Risk ratio=1.52) and cerebrovascular disease (Risk ratio =1.66). Although not significant, moderate drinker had lower ischemic heart disease mortality (Risk ratio =0.38). Among females, there was no statistically significant association between alcohol comsumption and mortality. CONCLUSION: The results of this study suggest that alcohol drinking has harmful effect on all-cause mortality, cardiovascular disease mortality and cerebrovascular disease mortality among males, especially in heavy drinker among males. Minimal evidence on protective effect for cardiovascular disease mortality in low or moderate drinker is observed.
Summary
Pesticides and Cancer Incidence: The Kangwha Cohort Study.
Jae Woong Sull, Sang Wook Yi, Tae Yong Sohn, Sun Ha Jee, Chung Mo Nam, Heechul Ohrr
Korean J Prev Med. 2002;35(1):24-32.
  • 2,431 View
  • 45 Download
AbstractAbstract PDF
OBJECTIVE
Few studies have examined the relationship between the risk of cancer and exposure to pesticides in Korea or in other East Asian that have until recently used chlorophenoxy herbicides. The aim of this study was to evaluate the relationship between the exposure to pesticides and cancer incidence. METHODS: We conducted a prospective cohort study with a follow-up period of 13 years (1985-1998). The subjects included 2,687 male and 3,589 female Kangwha Island residents, Koreans aged fifty-five or more as of March 1985, who received a personal health interview and completed a health examination survey. A Cox proportional hazards models were used to estimate relative risks (RR). RESULTS: At baseline, the mean age of the study participants in 1985 was 66.4 for males and 67.1 for females. During the 13 years follow-up, a total of 300 incidents of cancer in males and 146 in females developed. In males, the total cancer incidence in the highest group was RR, 1.4 (95% CI=1.0-1.9), p for trend=0.041, for digestive organ cancer incidence in the highest group, RR, 1.5 (95% CI=1.0-2.3), p for trend=0.057, for stomach cancer incidence in the highest group, RR, 1.6 (95% CI=0.9-2.8), p for trend=0.094, for gallbladder cancer incidence in the highest group, RR, 9.1 (95% CI=1.1-77.0), p for trend=0.014 were elevated according to the higher frequency of pesticide use per year. In particular, the risk of gallbladder cancer was very high. Although not significant, the risk of liver cancer was higher than in the non-exposed group (in the highest group, RR, 2.0 (95% CI=0.7-5.9)). In females, although not significant, breast cancer incidence in the highest exposure group was higher than in the non-exposed group (in the highest group, RR, 4.7 (95% CI=0.8-27.9)). CONCLUSIONS: This study demonstrates that Korean farmers who use pesticides, particularly males, have a significantly higher total cancer incidence, particularly from digestive organ cancers such as, stomach, gallbladder, and liver cancer. In particular, the risk of gallbladder cancer was very high.
Summary

JPMPH : Journal of Preventive Medicine and Public Health