Page 63 - GPD-1-1
P. 63
Gene & Protein in Disease Bangladesh genetic disease database
Nutr, 18(2): 121–127. https://doi.org/10.4103/2278-330X.119901
https://doi.org/10.5223/pghn.2015.18.2.121 120. Yesmin ZA, Nishat L, Banik D, et al., 2018, Current status in
108. Islam SS, Cader FA, Haq MM, et al., 2014, Williams medical genetics: Bangladesh perspective. Ann Int Med Dent
Syndrome presenting with supra valvular aortic stenosis: Res, 4(6): 10–14.
A case report. Ibrahim Card Med J, 4(1): 42–47. https://doi.org/10.21276/aimdr.2018.4.6.AT3
https://doi.org/10.3329/icmj.v4i1.52873 121. Lowrance WW, 2001, The promise of human genetic
109. Begum T, Mannan A, Khan MS, et al., 2006, Siblings with databases. BMJ, 322(7293): 1009–1010.
xeroderma pigmentosum: A case report. Bangladesh J Child https://doi.org/10.1136/bmj.322.7293.1009
Health, 30: 32–35.
122. Wall JD, Stawiski EW, Ratan A, et al., 2019, The GenomeAsia
https://doi.org/10.3329/bjch.v30i1.6182 100K Project enables genetic discoveries across Asia. Nature,
110. Moniruzzaman A, Absar M, Sarker S, et al., 2005, Xeroderma 576(7785): 106–111.
pigmentosum with squamous cell carcinoma: A case report and https://doi.org/10.1038/s41586-019-1793-z
literature review. Bangladesh J Child Health, 29(3): 104–106.
123. Bleich SN, Koehlmoos TL, Rashid M, et al., 2011,
https://doi.org/10.3329/bjch.v29i3.6189 Noncommunicable chronic disease in Bangladesh:
111. Khan MS, Jahan S, Paul SR, et al., 2019, A 19 month old male Overview of existing programs and priorities going forward.
child with xeroderma pigmentosum – A case report. Int J Health Policy (New York), 100(2–3): 282–289.
Clin Dermatol, 2(2): 15–18. https://doi.org/10.1016/j.healthpol.2010.09.004
https://doi.org/10.11648/j.ijcd.20190202.12 124. Bna.bh. 2022, Bahrain News Agency. Available
112. Bangaldesh Thalassemia Foundation. Available from: from: https://www.bna.bh/en/NationalGenome Center
https://www.thals.org/[Last accessed on 2021 Oct 27]. hopestocompletegenomeproject second phase by December.
aspx [Last accessed on 2022 Mar 07].
113. Ayub Q, Tyler-Smith C, 2009, Genetic variation in South
Asia: Assessing the influences of geography, language and 125. Ngdc.cncb.ac.cn. 2022, Databases - National Genomics Data
ethnicity for understanding history and disease risk. Brief Center (CNCB - NGDC). Available from: https://ngdc.cncb.
Funct Genomics, 8(5): 395–404. ac.cn/databases [Last accessed on 2022 Mar 07].
https://doi.org/10.1093/bfgp/elp015 126. 2022, Available from: https://www.dha.gov.ae/en/[Last
114. Noor FA, Sultana N, Bhuyan GS, et al., 2020, Nationwide accessed on 2022 Mar 07].
carrier detection and molecular characterization of 127. Diana N, 2017, The first modular database of Indonesian
β-thalassemia and hemoglobin E variants in Bangladeshi genes-associated diseases information. J Theor Appl Inf
population. Orphanet J Rare Dis, 15(1): 15. Technol, 95(6): 2017.
https://doi.org/10.1186/s13023-020-1294-z 128. Motazacker MM, Taherzadeh-Fard E, Husseini Z, et al.,
115. Sultana S, Hossain ML, Parvin MN, 2020, Pattern and 2007, The Iranian human mutation database. Arch Iran Med,
treatment of Parkinson’s disease at different health care 10(3): 372–375.
levels in Bangladesh: A hospital based survey. Int J Sci Rep, https://doi.org/07103/AIM.0016
6(4): 139–145.
129. Zlotogora J, van Baal S, Patrinos GP, 2009, The Israeli
https://doi.org/10.18203/issn.2454-2156.IntJSciRep20201269 National Genetic Database. Isr Med Assoc J, 11(6): 373–375.
116. Parkinson’s Disease in Bangladesh. Available from: https:// 130. Kamada M, Nakatsui M, Kojima R, et al., 2019, MGeND:
www.worldlifeexpectancy.com/bangladesh-parkinson- An integrated database for Japanese clinical and genomic
disease [Last accessed on 2021 Aug 14]. information. Hum Genome Var, 6(1): 53.
117. Akhter S, Hussain AH, Shefa J, et al., 2018, Prevalence of https://doi.org/10.1038/s41439-019-0084-4
Autism Spectrum Disorder (ASD) among the children aged
18-36 months in a rural community of Bangladesh: A cross 131. Park MH, Koo SK, Lee JS, et al., 2012, KMD: Korean
sectional study. F1000Research, 7: 424. mutation database for genes related to diseases. Hum Mutat,
33(4): E2332–E2340.
https://doi.org/10.12688/f1000research.13563.1
https://doi.org/10.1002/humu.22039
118. Autistic Children’s Welfare Foundation, Bangladesh.
Available from: http://www.acwf-bd.org/frequency_autism. 132. Halim-Fikri H, Etemad A, Abdul Latif AZ, et al., 2015,
php [Last accessed on 2021 Aug 14]. The first Malay database toward the ethnic-specific target
molecular variation. BMC Res Notes, 8(1): 176.
119. Hussain SM, 2013, Comprehensive update on cancer
scenario of Bangladesh. South Asian J Cancer, 2(4): 279–284. https://doi.org/10.1186/s13104-015-1123-y
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