MTHFR C677T and A1298C polymorphisms are risk factors for Down’s syndrome in Indian mothers AK Rai, S Singh, S Mehta, A Kumar, LK Pandey, R Raman Journal of human genetics 51 (4), 278-283, 2006 | 105 | 2006 |
Different population histories of the Mundari-and Mon-Khmer-speaking Austro-Asiatic tribes inferred from the mtDNA 9-bp deletion/insertion polymorphism in Indian populations K Thangaraj, V Sridhar, T Kivisild, AG Reddy, G Chaubey, VK Singh, ... Human genetics 116, 507-517, 2005 | 91 | 2005 |
A live cysticercosis in anterior chamber leading to glaucoma secondary to pupilary block A Chandra, MK Singh, VP Singh, AK Rai, S Chakraborty, OPS Maurya Journal of Glaucoma 16 (2), 271-273, 2007 | 20 | 2007 |
Choline metabolic pathway gene polymorphisms and risk for Down syndrome: an association study in a population with folate-homocysteine metabolic impairment SK Jaiswal, KK Sukla, A Chauhan, AR Lakhotia, A Kumar, AK Rai European journal of clinical nutrition 71 (1), 45-50, 2017 | 17 | 2017 |
Maternal risk for down syndrome and polymorphisms in the promoter region of the DNMT3B gene: A case–control study SK Jaiswal, KK Sukla, N Kumari, AR Lakhotia, A Kumar, AK Rai Birth Defects Research Part A: Clinical and Molecular Teratology 103 (4 …, 2015 | 17 | 2015 |
Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome P Chauhan, SK Jaiswal, AR Lakhotia, AK Rai Journal of assisted reproduction and genetics 33, 1161-1168, 2016 | 14 | 2016 |
Corneal stem cells niche and homeostasis impacts in regenerative medicine; concise review F Tavakkoli, TK Eleiwa, AM Elhusseiny, M Damala, AK Rai, K Cheraqpour, ... European journal of ophthalmology 33 (4), 1536-1552, 2023 | 12 | 2023 |
Complete androgen insensitivity syndrome due to mutations in the DNA-binding domain of the human androgen receptor gene P Chauhan, A Rani, SK Singh, AK Rai Sexual Development 12 (6), 269-274, 2018 | 11 | 2018 |
Two familial cases of Robertsonian transloacations 13; 14 and its clinical consequences SK Jaiswal, A Upadhyay, A Ali, SK Upadhyay, A Kumar, A Rai J Genet Syndr Gene Ther 7 (1), 1-4, 2016 | 9 | 2016 |
Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies SK Jaiswal, A Kumar, A Ali, AK Rai Gene 559 (1), 94-98, 2015 | 8 | 2015 |
Transcriptomic profiling of human limbus-derived stromal/mesenchymal stem cells—novel mechanistic insights into the pathways involved in corneal wound healing F Tavakkoli, M Damala, MA Koduri, A Gangadharan, AK Rai, D Dash, ... International Journal of Molecular Sciences 23 (15), 8226, 2022 | 7 | 2022 |
Association of genetic polymorphisms in genes involved at the branch point of nucleotide biosynthesis and remethylation with down syndrome birth risk: a case-control study SK Jaiswal, KK Sukla, SK Mishra, AR Lakhotia, A Kumar, AK Rai J Mol Genet Med 10 (207), 1747-0862.1000207, 2016 | 7 | 2016 |
Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study SK Jaiswal, KK Sukla, V Gupta, AK Rai Journal of genetics 93, 865-868, 2014 | 7 | 2014 |
Clinical, hematological, and cytogenetic profile of aplastic anemia S Das, V Tilak, V Gupta, A Singh, M Kumar, A Rai The Egyptian Journal of Haematology 40 (1), 3-10, 2015 | 6 | 2015 |
Hepatocellular carcinoma presenting as neutrophilic leukaemoid reaction--a rare entity. V Tilak, M Rai, VP Singh, AK Rai, R Raman Journal of the Indian Medical Association 105 (8), 462, 464-5, 2007 | 6 | 2007 |
Molecular cytogenetic classification of down syndrome and screening of somatic aneuploidy in mothers SK Jaiswal, A Kumar, AK Rai Cytogenetic and Genome Research 161 (8-9), 397-405, 2021 | 2 | 2021 |
Adoption Behaviour of Farmers about Recommended Wheat Production Practices in Prayagrag District of Uttar Pradesh DK Bose, OP Maurya, AK Rai Small (up to 1 ha) 67, 55.83, 0 | 2 | |
Identification of Novel Nucleotide Changes in INHBB Gene by Mutation Screening in Females with Ovarian Dysgenesis: A Case Report P Chauhan, A Rani, AK Rai Journal of Reproduction & Infertility 22 (4), 295, 2021 | 1 | 2021 |
Identification of human limbal stem cell by p63, a specific stem cell marker in cadaveric limbal tissue and in in-vitro limbal stem culture D Prakash, A Rai, S Patne, S Kumar, OPS Maurya, A Chandra The Journal of Community Health Management 2 (1), 33-42, 2015 | 1 | 2015 |
Molecular cytogenetic analysis using FISH and HD-oligo micro array identified an unusual novel Down syndrome caseMolecular cytogenetic analysis using FISH and HD-oligo micro … SK Jaiswal, AK Rai World Journal of Biology Pharmacy and Health Sciences 14 (2), 320-328, 2023 | | 2023 |