[1]
Xing J , Wuren T, Simonson TS , Watkins WS, Witherspoon DJ , Wu W , Qin G , Huff CD, Jorde LB , Ge R . 2013. Genomic Analysis of Natural Selection and Phenotypic Variation in High-Altitude Mongolians. PLoS Genet. 9 (7) :1-13.
DOI: 10.1371/journal.pgen.1003634
Google Scholar
[2]
Pitchappan RM. 2002. Castes, Migration, Immunogenetics and infectious diseases in South India. Community Genetics. 5: 157-161.
DOI: 10.1159/000066329
Google Scholar
[3]
Tamang R and Thangaraj K. 2012.Genomic view on the peopling of India. Investigative Genetics. 3 : 20 :1-9.
DOI: 10.1186/2041-2223-3-20
Google Scholar
[4]
Sugunan AP, Ghosh AR, Subarna Roy, Gupte MD, and Sehgal SC. 2004. A cholera epidemic among the nicobarese tribe of nancowry, andaman, and nicobar, India. Am. J. Trop. Med. Hyg. 71(6). p.822–827.
DOI: 10.4269/ajtmh.2004.71.822
Google Scholar
[5]
Haimanti Bhattacharya, Debdutta Bhattacharya, Subarna Roy, and Sugunan AP. 2014. Occult hepatitis B infection among individuals belonging to the aboriginal Nicobarese tribe of IndiaJ Infect Dev Ctries. 8 (12) :1630-1635.
DOI: 10.3855/jidc.4350
Google Scholar
[6]
Sharma PR, ain S, Bamezai R N K and Tiwari1 P K. 2010. Utility of serum ldh isoforms in the assessment ofmycobacterium tuberculosis induced pathology in tb patients ofsahariya tribe Indian Journal of Clinical Biochemistry. 25 (1) 57-63.
DOI: 10.1007/s12291-010-0012-3
Google Scholar
[7]
Balgir RS. 2010. Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India J Community Genet . 1:117–123
DOI: 10.1007/s12687-010-0016-y
Google Scholar
[8]
Deepak Bharti, Ashish Kumar, Ranjeet Singh Mahla, Sushil Kumar, Harshad Ingle, Tushar Yadav,Anamika Mishra, Ashwin Ashok Raut and Himanshu Kuma. 2015. Low prevalence of CCR5‑Δ32, CCR2‑64I and SDF1‑3'A alleles in the Baiga and Gond tribes of Central India . SpringerPlus. 4: 451 DOI 10. 1186/s40064-015- 1238-6.
DOI: 10.1186/s40064-015-1238-6
Google Scholar
[9]
Murhekar MV, Murhekar KM . Arankalle VA . and Sehgal. SC. 2002. Epidemiology of hepatitis B infection among the Nicobarese a mongoloid tribe of the Andaman and Nicobar Islands, India Epidemiol. Infect.128, 465 – 471. DOI:10.1017}S095026880200691X
DOI: 10.1017/s095026880200691x
Google Scholar
[10]
Ruchira Chaudhary and Gunjan Sharma. 2010 Genetic assessment of serological and biochemical markers in Bharia tribe of Chhindwara district of Madhya Pradesh. Indian Journal of Human Genetics . Vol.16 Iss. 3
DOI: 10.4103/0971-6866.73401
Google Scholar
[11]
Sharma G, Tamang R, Chaudhary R, Singh VK, Shah AM, Anugula S, Rani DS, Reddy AG, Eaaswarkhanth M, Chaubey G, Singh L and Thangaraj K. 2012. Genetic Affinities of the Central Indian Tribal Populations. PLoS ONE 7(2): e32546.
DOI: 10.1371/journal.pone.0032546
Google Scholar
[12]
Bhuniya S, Maji D, Mandal D and Mondal N. 2013. Measles outbreak among the Dukpa tribe of Buxa hills in West Bengal, India: Epidemiology and vaccine effi cacy. Indian J Public Health . 57:272-5
DOI: 10.4103/0019-557x.123273
Google Scholar
[13]
Ashok K. Kayal, Munindra Goswami, Marami Das, and Hussain Masaraf. 2011. A case of Spinocerebellar Ataxia from ethnic tribe of Assam. Ann Indian Acad Neuro.14: 122-3
DOI: 10.4103/0972-2327.82802
Google Scholar
[14]
Rao VG, Gopi PG, Bhat J, Selvakumar N, Yadav R, Tiwari B, Gadge V, Bhondeley MK, and Wares F. 2010. Pulmonary tuberculosis: a public health problem amongst the Saharia, a primitive tribe of Madhya Pradesh, Central India International Journal of Infectious Diseases. 14 e713–e716.
DOI: 10.1016/j.ijid.2010.02.2243
Google Scholar
[15]
Krithika S, Maji S and Vasulu TS. 2008. A Microsatellite Guided Insight into the Genetic Status of Adi, an Isolated Hunting-Gathering Tribe of Northeast India. PLoS ONE . 3(7): e2549. doi:10.1371 / journal.pone.0002549.
DOI: 10.1371/journal.pone.0002549
Google Scholar
[16]
Rao VG, Gopi PG, Bhat J, Yadav R, Selvakumar N, and Wares DF. 2010. Selected risk factors associated with pulmonary tuberculosis among Saharia tribe of Madhya Pradesh, central India European Journal of Public Health. Vol. 22, No. 2, 273 – 278.
DOI: 10.1093/eurpub/ckr009
Google Scholar
[17]
Thurston E and Rangachari K . Castes and Tribes of Southern India. 1909. I -V I I (A and Z), Madras: Government Press. Retrieved 2011.
Google Scholar
[18]
Singh KS. The Scheduled Tribes . Anthropological Survey of India, 1992. (National Series Vol. III). Oxforod University Press. Retrieved 2010.
Google Scholar
[19]
Vishwanathan H, Edwin D, Cordaux R, Stoneking M, Usha Rani MV. and Majumder PP. 2004. Genetic structure and affinitiesamong tribal populations of southern India: a study of 24 auto-somal DNA markers.Ann. Hum. Genet. 68, 128–138.
DOI: 10.1046/j.1529-8817.2003.00083.x
Google Scholar
[20]
Kanthimathi A, Vijaya M, and Ramesh A. 2008. Genetic study of Dravidian caste of Tamil Nadu. J Genet. 87(2) : 175-179.
DOI: 10.1007/s12041-008-0027-1
Google Scholar
[21]
Deva A, Nandakumar R, Raghu P and Prabhakaran K. 2016. Autosomal DNA Polymorphisms of Four South India Tribal Populations. WSN (2016). 35.62-72.
Google Scholar
[22]
Fei Zhou Y, Yan Y, Ping Hou X, Miao J, Zhang J, Xiang Yin Q, Jie L J, Xiao- Zhang Y,Yuan Li and Yand Lan Luo H. 2013. Association study of Angiotensin converting enzyme gene polymorphism with elderly diabetic hypertension and lipids levels. Lipids in Health and Disease 12:187.
DOI: 10.1186/1476-511x-12-187
Google Scholar
[23]
Xia H, Sriramula S, Chhabra KH and Lazartigues E. 2013. Brain Angiotensin-converting enzyme type shedding contributes to the development of neurogenic hypertension. Circ Res 113(9):1087–96.
DOI: 10.1161/circresaha.113.301811
Google Scholar
[24]
Chaoxin J, Daili S, Yanxin H, Ruwei G, Chenlong W and Yaobin T. 2013. The influence of angiotensin-converting enzyme 2 gene polymorphisms on type 2 diabetes mellitus and coronary heart disease. Eur Rev Med PharmacolSci. 17(19):2654–9.
Google Scholar
[25]
Muñoz-Barrios S, Guzmán-Guzmán IP, Muñoz-Valle JF, Salgado-Bernabé AB, Salgado-Goytia L and Parra-Rojas I. 2012. Association of the HindIII and S447X polymorphisms in LPL gene with hypertension and type 2 diabetes in Mexican families. Dis Markers. 33 (6) : 313–20.
DOI: 10.1155/2012/673452
Google Scholar
[26]
Zarouk WA, Hussein IR, Esmaeil NN, Raslan HM, Reheim HA, Moguib O, Emara NA, Aly AA, and Hamed M. 2012. Association of angiotensin converting enzyme gene (I/D) polymorphism with hypertension and type 2 diabetes. Bratisl Lek Listy . 113 (1) :14–8.
DOI: 10.4149/bll_2012_003
Google Scholar
[27]
Al-Rubeaan K, Siddiqui K, Saeb AT, Nazir N, Al-Naqeb D, Al-Qasim S. 2013. ACE I/D and MTHFR C677T polymorphisms are significantly associated with type 2 diabetes in Arab ethnicity: a meta-analysis. Gene. 520 (2) : 166 –77.
DOI: 10.1016/j.gene.2013.02.017
Google Scholar
[28]
Al-Harbi EM, Farid EM, Gumaa KA, Darwish AH, Alenizi M and Singh J. 2013. Genetic combination of angiotensin-converting enzyme with methylene tetrahydrofolate reductase polymorphisms and the risk of type 2 diabetes mellitus in Bahrain. J Renin Angiotensin Aldosterone Syst
DOI: 10.1177/1470320313478286
Google Scholar
[29]
Purnamasari D, Widjojo BD, Antono D, and Syampurnawati M. 2012. ACE gene polymorphism and atherosclerotic lesion of carotid artery among off springs of type 2 diabetes mellitus. Acta Med Indones . 44 (2) :128–34.
Google Scholar
[30]
Narne P, Ponnaluri KC, Singh S, Siraj M, and Ishaq M. 2012. Relationship between angiotensin-converting enzyme gene insertion/deletion polymorphism, angiographically defined coronary artery disease and myocardial infarction in patients with type 2 diabetes mellitus. J Renin Angiotensin Aldosterone Syst. 13 (4) : 478–86.
DOI: 10.1177/1470320312448947
Google Scholar
[31]
Sinorita H, Madiyan M, Pramono RB, Purnama LB, Ikhsan MR and Asdie AH. 2010. ACE gene insertion/deletion polymorphism among patients with type 2 diabetes, and its relationship with metabolic syndrome at Sardjito Hospital Yogyakarta, Indonesia. Acta Med Indones . 42(1):12–6.
Google Scholar
[32]
Niu W, Qi Y, Gao P, and Zhu D. 2010. Angiotensin converting enzyme D allele is associated with an increased risk of type 2 diabetes: evidence from a meta-analysis. Endocr J . 57 (5) : 431–8.
DOI: 10.1507/endocrj.k09e-360
Google Scholar
[33]
Chmaisse HN, Jammal M, Fakhoury H, and Fakhoury R. 2009. A study on the association between angiotensin-I converting enzyme I/D dimorphism and type-2 diabetes mellitus. Saudi J Kidney Dis Transpl. 20 (6) : 1038 – 46.
DOI: 10.4103/1319-2442.202789
Google Scholar
[34]
Rasyid H, Bakri S, and Yusuf I. 2012. Angiotensin-converting enzyme gene polymorphisms, blood pressure and pulse pressure in subjects with essential hypertension in a South Sulawesi Indonesian population. Acta Med Indones . 44 (4) : 280 –3.
Google Scholar
[35]
Zhu M, Zhang J, Nie S and Yan W. 2012 Associations of ACE I/D, AGT M235T gene polymorphisms with pregnancy induced hypertension in Chinese population: a meta-analysis. J Assist Reprod Genet . 29 (9) : 921–32.
DOI: 10.1007/s10815-012-9800-4
Google Scholar
[36]
Miller SA, Dykes DD and Poesky HF 1988. A Simple Salting Out Procedure Form Extracting DNA From Human Nucleated Cells. Nucleic Acids Res.70: 3321- 3323.
DOI: 10.1093/nar/16.3.1215
Google Scholar
[37]
Stoneking M, Fontius JJ, Clifford SL, Soodyall H, Arcot S et al.1997. Alu insertion/ deletion polymorphism and human evolution: Evidence for a larger population size in Africa. Genome Res. 7: 1061- 1071.
DOI: 10.1101/gr.7.11.1061
Google Scholar
[38]
Majumder PP, Roy B, Banerjee S, Chakraborty M, Dey B et al.1997. Human - specific insertion/deletion polymorphisms in Indian populations and their possible evolutionary implications. Eur J Hum Genet. 7: 435-446
DOI: 10.1038/sj.ejhg.5200317
Google Scholar
[39]
Yeh FC, and Yang RC. A Joint Project Development: POPGENE 1.32. Centre for International Forestry Research. Canada: University of Alberta and TimBoyle. 1999.
Google Scholar
[40]
Cowie CC, Port FK, Wolfe RA, Savage PJ, Moll PP and Hawthorne VM. 1989. Disparities in incidence of diabetic end-stage renal disease according to race and type of diabetes. N Engl J Med. 321: 1074–9.
DOI: 10.1056/nejm198910193211603
Google Scholar
[41]
Zhu M, Zhang J, Nie S and Yan W. 2012. Associations of ACE I/D, AGT M235T gene polymorphisms with pregnancy induced hypertension in Chinese population: a meta-analysis. J Assist Reprod Genet . 29 (9) : 921–32.
DOI: 10.1007/s10815-012-9800-4
Google Scholar
[42]
Haynes SR, Toomey TP, Leinwand L, and Jelinek WR. 1981. The Chinese Hamster Alu-Equivalent Sequence: a Conserved, Highly Repetitious, Interspersed Deoxyribonucleic Acid Sequence in Mammals Has a Structure Suggestive of a Transposable Element. Moleu. and cellu. Bio. 1(7) pp.573-583
DOI: 10.1128/mcb.1.7.573-583.1981
Google Scholar
[43]
Houck CM, Rinehart FP and Schmid CW. 1979. A ubiquitous family of repeated DNA sequences in the human genome. J Mol Biol .132: 289–306.
DOI: 10.1016/0022-2836(79)90261-4
Google Scholar
[44]
Comas D, Calafell F, Benchemsi N, Helal A, Lefranc G, Stoneking M, Batzer MA, Bertranpetit J and Sajantila A. 2000. Alu insertion polymorphisms in NW Africa and the Iberian Peninsula:evidence for a strong genetic boundary through the Gibraltar Straits. Hum Genet.107: 312-319.
DOI: 10.1007/s004390000370
Google Scholar
[45]
Nasidze I, Risch GM, Robichaux M, Sherry ST, Batzer MA and Stoneking M. 2001. Alu insertion polymorphisms and the genetic structure of human populations from theCaucasus. Eur J Hum Genet. 9: 267-272.
DOI: 10.1038/sj.ejhg.5200615
Google Scholar
[46]
Harun Mustafa, Matei David and Michael Brudno. 2014. Assembly and characterization of novel Alu inserts detected from next-generation sequencing data. Mobile Genetic Elements 4:5. 17.
DOI: 10.4161/21592543.2014.969584
Google Scholar
[47]
Schilter KF, Reis LM, Sorokina EA and Semina EV. 2015. Identification of an Alu-repeat-mediated deletion of OPTN upstream region in a patient with a complex ocularphenotype. Molecular Genetics & Genomic Medicine. 3(6): 490 – 499.
DOI: 10.1002/mgg3.159
Google Scholar
[48]
Wildschutte JH, Baron A, Diroff NM, Kidd JM. 2015. Discovery and characterization of Alu repeat sequences via precise local read assembly. Nucleic Acids Research.43.(21).
DOI: 10.1093/nar/gkv1089
Google Scholar
[49]
Rishishwar L,Tellez Villa CL and King Jordan I. 2015. Transposable element polymorphisms recapitulate human evolution. Mobile DNA . 6:21.
DOI: 10.1186/s13100-015-0052-6
Google Scholar
[50]
Siu-Kin Ng, Taobo Hu, Xi Long, Cheuk-Hin Chan, Shui-Ying Tsang and Hong Xue. 2016. Feature co-localization landscape of the human genome. Scientific Reports. 6:20650.
DOI: 10.1038/srep20650
Google Scholar
[51]
Qian Y, Kehr B and Halld Orsson BV.2015 .PopAlu: population-scale detection of Alu polymorphisms. Peer J .3:e1269.
DOI: 10.7717/peerj.1269
Google Scholar
[52]
Sang-Je Park, Young-Hyun Kim, Sang-Rae Lee, Se-Hee Choe, Myung-Jin Kim, Sun-Uk Kim,Ji-Su Kim, Bo-Woong Sim, Bong-Seok Song, Kang-Jin Jeong, Yeung-Bae Jin, Youngjeon Lee1 Young-Ho Park, Young Il Park, Jae-Won Huh and Kyu-Tae Chang. 2015. Gain of a New Exon by a Lineage-Specific Alu Element-Integration Event in the BCS1L Gene during Primate Evolution. Mol. Cells . 38(11): 950958m.
DOI: 10.14348/molcells.2015.0121
Google Scholar
[53]
Kaur S and Pociot F. 2015. Alu Elements as Novel Regulators of Gene Expression in Type I Diabetes Susceptibility Genes?.Genes 2015. 6. 577-591;.
DOI: 10.3390/genes6030577
Google Scholar
[54]
Zhou D, Ruiter R, Zhang J, Zhou M, Liu H, Liu W and Wang S 2012. Angiotensin converting enzyme I/D polymorphism is not associated with type 2 diabetes in a Chinese population. J Renin Angiotensin Aldosterone Syst. 13 : 372–8.
DOI: 10.1177/1470320311435535
Google Scholar
[55]
Bhaskar LV, Mahin S and Ginila RT, Soundararajan P. 2013. Role of the ACE ID and PPARG P12A Polymorphisms in Genetic Susceptibility of Diabetic Nephropathy in a South Indian Population. Nephrourol Mon. 5 (3) : 813–817.
DOI: 10.5812/numonthly.9573
Google Scholar
[56]
Woo SW, Bang S, Chung MW, Jin SK, Kim YS and Lee SH. 2009. Lack of association between ACE and bradykinin B2 receptor gene polymorphisms and ACE inhibitor-induced coughing in hypertensive Koreans. J Clin Pharm Ther . 34 (5) :561–7.
DOI: 10.1111/j.1365-2710.2009.01028.x
Google Scholar
[57]
He Q, Fan C, Yu M, Wallar G, Zhang ZF, Wang L, Zhang X and Hu R 2013. Associations of ACE Gene Insertion/Deletion Polymorphism, ACE Activity, and ACE mRNA Expression with Hypertension in a Chinese Population. PLoS One . 8(10):e75870.
DOI: 10.1371/journal.pone.0075870
Google Scholar
[58]
Zivko M, Kusec R and Galesić K. 2013. Impact of angiotensin-converting enzyme gene polymorphism on proteinuria and arterial hypertension. Coll Antropol. 37:765–770.
Google Scholar
[59]
Haque SF, Ahmad M, Khan AU, Gupta V and Khan AS. 2010. ACE Insertion / Detetion gene polymorphism and sequence in Diabetic nephropathy. Int J Diabetes & Matab . 18:14 – 118.
Google Scholar