Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Liu, Jimmy Z, van Sommeren, Suzanne, Huang, Hailiang, Ng, Siew C, Alberts, Rudi, Takahashi, Atsushi, Ripke, Stephan, Lee, James C, Jostins, Luke, Shah, Tejas, Abedian, Shifteh, Cheon, Jae Hee, Cho, Judy, Daryani, Naser E, Franke, Lude, Fuyuno, Yuta, Hart, Ailsa, Juyal, Ramesh C, Juyal, Garima, Kim, Won Ho, Morris, Andrew P, Poustchi, Hossein, Newman, William G, Midha, Vandana, Orchard, Timothy R, Vahedi, Homayon, Sood, Ajit, Sung, Joseph J Y, Malekzadeh, Reza, Westra, Harm-Jan, Yamazaki, Keiko, Yang, Suk-Kyun, Barrett, Jeffrey C, Franke, Andre, Alizadeh, Behrooz Z, Parkes, Miles, B K, Thelma, Daly, Mark J, Kubo, Michiaki, Anderson, Carl A, Weersma, Rinse K
Published in Nature genetics (01.09.2015)
Published in Nature genetics (01.09.2015)
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Association of TGFβ1, TNFα, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian Indians
Prasad, Pushplata, Tiwari, Arun K, Kumar, KM Prasanna, Ammini, AC, Gupta, Arvind, Gupta, Rajeev, Thelma, BK
Published in BMC medical genetics (12.04.2007)
Published in BMC medical genetics (12.04.2007)
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Association analysis of ADPRT1, AKR1B1, RAGE, GFPT2 and PAI-1 gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes
Prasad, Pushplata, Tiwari, Arun K, Kumar, K M Prasanna, Ammini, A C, Gupta, Arvind, Gupta, Rajeev, Thelma, B K
Published in BMC medical genetics (31.03.2010)
Published in BMC medical genetics (31.03.2010)
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De novo deletion in MECP2 in a monozygotic twin pair: a case report
Mittal, Kirti, Kabra, Madhulika, Juyal, Ramesh, BK, Thelma
Published in BMC medical genetics (27.08.2011)
Published in BMC medical genetics (27.08.2011)
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Chronic renal insufficiency among Asian Indians with type 2 diabetes: I. Role of RAAS gene polymorphisms
Prasad, Pushplata, Tiwari, Arun K, Kumar, K M Prasanna, Ammini, A C, Gupta, Arvind, Gupta, Rajeev, Sharma, A K, Rao, A R, Nagendra, R, Chandra, T Satish, Tiwari, S C, Rastogi, Priyanka, Gupta, B Lal, Thelma, B K
Published in BMC medical genetics (03.05.2006)
Published in BMC medical genetics (03.05.2006)
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Pre-prescription testing in psychiatry: An overview
Mukhopadhyay, Anirban, Rai, Chandra Bhushan, Deshpande, Smita N, Thelma, BK
Published in Open journal of psychiatry & allied sciences (01.12.2022)
Published in Open journal of psychiatry & allied sciences (01.12.2022)
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An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians
Juyal, Garima, Prasad, Pushplata, Senapati, Sabyasachi, Midha, Vandana, Sood, Ajit, Amre, Devendra, Juyal, Ramesh C, BK, Thelma
Published in PloS one (31.01.2011)
Published in PloS one (31.01.2011)
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SA120FAMILY BASED RARE VARIANT STUDY SUPPORTS THE CUMULATIVE CONTRIBUTION OF NEURODEVELOPMENTAL PATHWAY GENES IN SCHIZOPHRENIA ETIOLOGY
Thelma, BK, John, Jibin, Kukshal, Prachi, Bhatia, Triptish, Nimgaonkar, Vishwajit, Deshpande, Smita
Published in European neuropsychopharmacology (2019)
Published in European neuropsychopharmacology (2019)
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Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism
Sudhaman, Sumedha, Prasad, Kameshwar, Behari, Madhuri, Muthane, Uday B, Juyal, Ramesh C, Thelma, BK
Published in Journal of medical genetics (01.07.2016)
Published in Journal of medical genetics (01.07.2016)
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Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study
Chowdhury MadhumitaRoy, Kabra Madhulika, Sharma Deepti, Singh Deepika, Dabral Anjali, Thelma BK, Kalra Veena
Published in Indian journal of human genetics (01.01.2006)
Published in Indian journal of human genetics (01.01.2006)
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Association of regulatory variants of dopamine β-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects
Punchaichira, Toyanji J, Mukhopadhyay, Anirban, Kukshal, Prachi, Bhatia, Triptish, Deshpande, Smita N, Thelma, B K
Published in Journal of psychopharmacology (Oxford) (01.03.2020)
Published in Journal of psychopharmacology (Oxford) (01.03.2020)
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Findings From Continuing Gene Hunt In Families With Schizophrenia
Thelma, BK, John, Jibin, Kukshal, Prachi, Bhatia, Triptish, Nimgaonkar, V L, Deshpande, S N
Published in European neuropsychopharmacology (2017)
Published in European neuropsychopharmacology (2017)
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Factors Associated with Transient Neonatal Hyperthyrotropinemia
Garg, Ritika, Sait, Haseena, Jindal, Ankur, Juneja, Monica, Gupta, Sangeeta, Thelma, BK, Kapoor, Seema
Published in Indian journal of pediatrics (01.06.2020)
Published in Indian journal of pediatrics (01.06.2020)
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Targeted Deep Resequencing Identifies MID2 Mutation for X-Linked Intellectual Disability with Varied Disease Severity in a Large Kindred from India
Geetha, Thenral S., Michealraj, Kulandaimanuvel Antony, Kabra, Madhulika, Kaur, Gurjit, Juyal, Ramesh C., Thelma, B.K.
Published in Human mutation (01.01.2014)
Published in Human mutation (01.01.2014)
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