Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide
Stuart, Philip E., Tsoi, Lam C., Nair, Rajan P., Ghosh, Manju, Kabra, Madhulika, Shaiq, Pakeeza A., Raja, Ghazala K., Qamar, Raheel, Thelma, B.K., Patrick, Matthew T., Parihar, Anita, Singh, Sonam, Khandpur, Sujay, Kumar, Uma, Wittig, Michael, Degenhardt, Frauke, Tejasvi, Trilokraj, Voorhees, John J., Weidinger, Stephan, Franke, Andre, Abecasis, Goncalo R., Sharma, Vinod K., Elder, James T.
Published in HGG advances (13.01.2022)
Published in HGG advances (13.01.2022)
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Journal Article
Enantiodivergent synthesis of (−)-methylenolactocin and (+)-methylenolactocin from d-mannitol
Ghosh, Manju, Bose, Sritama, Maity, Soumitra, Ghosh, Subrata
Published in Tetrahedron letters (16.12.2009)
Published in Tetrahedron letters (16.12.2009)
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Journal Article
Novel non-identical MECP2 mutations in Rett syndrome family: A rare presentation
Khajuria, Rajni, Gupta, Neerja, Sapra, Savita, Gulati, Sheffali, Ghosh, Manju, Kalra, Veena, Kabra, Madhulika
Published in Brain & development (Tokyo. 1979) (01.01.2012)
Published in Brain & development (Tokyo. 1979) (01.01.2012)
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Journal Article
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC
AHMED, Zubair M, SMITH, Tenesha N, FRIEDMAN, Thomas B, WILCOX, Edward R, RIAZUDDIN, Saima, MAKISHIMA, Tomoko, GHOSH, Manju, BOKHARI, Sirosh, MENON, Puthezhath S. N, DESHMUKH, Dilip, GRIFFITH, Andrew J, RIAZUDDIN, Sheikh
Published in Human genetics (01.06.2002)
Published in Human genetics (01.06.2002)
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Journal Article
Molecular Genetic Studies in Indian Patients With Megalencephalic Leukoencephalopathy
Shukla, Pallavi, PhD, Gupta, Neerja, MD, Ghosh, Manju, MD, Vasisht, Suman, PhD, Gulati, Sheffali, MD, Balakrishnan, Prahlad, PhD, Sharma, Raju, MD, Gupta, Arun K., MD, Kamate, Mahesh, MD, Kalra, Veena, MD, Kabra, Madhulika, MD
Published in Pediatric neurology (01.06.2011)
Published in Pediatric neurology (01.06.2011)
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Journal Article
In vivo assessment of toxicity and pharmacokinetics of methylglyoxal
Ghosh, Manju, Talukdar, Dipa, Ghosh, Swapna, Bhattacharyya, Nivedita, Ray, Manju, Ray, Subhankar
Published in Toxicology and applied pharmacology (01.04.2006)
Published in Toxicology and applied pharmacology (01.04.2006)
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Journal Article
Sequential occurrence of preneoplastic lesions and accumulation of loss of heterozygosity in patients with gallbladder stones suggest causal association with gallbladder cancer
Jain, Kajal, Mohapatra, Trilochan, Das, Prasenjit, Misra, Mahesh Chandra, Gupta, Siddhartha Datta, Ghosh, Manju, Kabra, Madhulika, Bansal, Virinder Kumar, Kumar, Subodh, Sreenivas, Vishnubhatla, Garg, Pramod Kumar
Published in Annals of surgery (01.12.2014)
Published in Annals of surgery (01.12.2014)
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Journal Article
Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients – A study from a tertiary care genetic centre in India
Sharma, Pankaj, Gupta, Neerja, Chowdhury, Madhumita Roy, Sapra, Savita, Ghosh, Manju, Gulati, Sheffali, Kabra, Madhulika
Published in Gene (15.09.2016)
Published in Gene (15.09.2016)
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Journal Article
Identification of a novel homozygous mutation in transmembrane channel like 1 ( TMC1 ) gene, one of the second-tier hearing loss genes after GJB2 in India
Singh, Pawan Kumar, Ghosh, Manju, Sharma, Shipra, Shastri, Shivaram, Gupta, Neerja, Chowdhury, Madhumita Roy, Anand, Anuranjan, Kabra, Madhulika
Published in Indian journal of medical research (New Delhi, India : 1994) (01.04.2017)
Published in Indian journal of medical research (New Delhi, India : 1994) (01.04.2017)
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Journal Article
Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
Schultz, Julie M, Bhatti, Rashid, Madeo, Anne C, Turriff, Amy, Muskett, Julie A, Zalewski, Christopher K, King, Kelly A, Ahmed, Zubair M, Riazuddin, Saima, Ahmad, Nazir, Hussain, Zawar, Qasim, Muhammad, Kahn, Shaheen N, Meltzer, Meira R, Liu, Xue Z, Munisamy, Murali, Ghosh, Manju, Rehm, Heidi L, Tsilou, Ekaterini T, Griffith, Andrew J, Zein, Wadih M, Brewer, Carmen C, Riazuddin, Sheikh, Friedman, Thomas B
Published in Journal of medical genetics (01.11.2011)
Published in Journal of medical genetics (01.11.2011)
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Journal Article
Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39
Schultz, Julie M., Khan, Shaheen N., Ahmed, Zubair M., Riazuddin, Saima, Waryah, Ali M., Chhatre, Dhananjay, Starost, Matthew F., Ploplis, Barbara, Buckley, Stephanie, Velásquez, David, Kabra, Madhulika, Lee, Kwanghyuk, Hassan, Muhammad J., Ali, Ghazanfar, Ansar, Muhammad, Ghosh, Manju, Wilcox, Edward R., Ahmad, Wasim, Merlino, Glenn, Leal, Suzanne M., Riazuddin, Sheikh, Friedman, Thomas B., Morell, Robert J.
Published in American journal of human genetics (10.07.2009)
Published in American journal of human genetics (10.07.2009)
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Journal Article
Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India
Sharma, Pankaj, Gupta, Neerja, Chowdhury, Madhumita R., Phadke, Shubha R., Sapra, Savita, Halder, Ashutosh, Ghosh, Manju, Kabra, Madhulika
Published in Cytogenetic and genome research (01.11.2015)
Published in Cytogenetic and genome research (01.11.2015)
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Journal Article
Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide
Stuart, Philip E, Tsoi, Lam C, Nair, Rajan P, Ghosh, Manju, Kabra, Madhulika, Shaiq, Pakeeza A, Raja, Ghazala K, Qamar, Raheel, Thelma, B K, Patrick, Matthew T, Parihar, Anita, Singh, Sonam, Khandpur, Sujay, Kumar, Uma, Wittig, Michael, Degenhardt, Frauke, Tejasvi, Trilokraj, Voorhees, John J, Weidinger, Stephan, Franke, Andre, Abecasis, Goncalo R, Sharma, Vinod K, Elder, James T
Published in HGG advances (13.01.2022)
Published in HGG advances (13.01.2022)
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Journal Article
Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function
Griffith, Andrew J, Kurima, Kiyoto, Peters, Linda M, Yang, Yandan, Riazuddin, Saima, Ahmed, Zubair M, Naz, Sadaf, Arnaud, Deidre, Drury, Stacy, Mo, Jianhong, Makishima, Tomoko, Ghosh, Manju, Menon, P.S.N, Deshmukh, Dilip, Oddoux, Carole, Ostrer, Harry, Khan, Shaheen, Riazuddin, Sheikh, Deininger, Prescott L, Hampton, Lori L, Sullivan, Susan L, Battey, James F, Keats, Bronya J.B, Wilcox, Edward R, Friedman, Thomas B
Published in Nature genetics (01.03.2002)
Published in Nature genetics (01.03.2002)
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Journal Article
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing
Nal, Nevra, Ahmed, Zubair M, Erkal, Engin, Alper, Özgül M, Lüleci, Güven, Dinç, Oktay, Waryah, Ali Muhammad, Ain, Quratul, Tasneem, Saba, Husnain, Tayyab, Chattaraj, Parna, Riazuddin, Saima, Boger, Erich, Ghosh, Manju, Kabra, Madhulika, Riazuddin, Sheikh, Morell, Robert J, Friedman, Thomas B
Published in Human mutation (01.10.2007)
Published in Human mutation (01.10.2007)
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Journal Article
In vivo assessment of toxicity and pharmacokinetics of methylglyoxal Augmentation of the curative effect of methylglyoxal on cancer-bearing mice by ascorbic acid and creatine
GHOSH, Manju, TALUKDAR, Dipa, GHOSH, Swapna, BHATTACHARYYA, Nivedita, RAY, Manju, RAY, Subhankar
Published in Toxicology and applied pharmacology (01.04.2006)
Published in Toxicology and applied pharmacology (01.04.2006)
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Journal Article