Rajesh Thakker (English Wikipedia)

Anon (2014). "Thakker, Prof. Rajesh Vasantlal". Who's Who (online edition via Oxford University Press ed.). A & C Black. doi:10.1093/ww/9780199540884.013.U37302. (Subscription or UK public library membership required.)
Holmes, David (2013). "Rajesh Thakker: A man of hidden depths". The Lancet Diabetes & Endocrinology. 1 (4): 274. doi:10.1016/S2213-8587(13)70196-7. PMID 24622412.
Lloyd, S. E.; Pearce, S. H.; Fisher, S. E.; Steinmeyer, K; Schwappach, B; Scheinman, S. J.; Harding, B; Bolino, A; Devoto, M; Goodyer, P; Rigden, S. P.; Wrong, O; Jentsch, T. J.; Craig, I. W.; Thakker, R. V. (1996). "A common molecular basis for three inherited kidney stone diseases". Nature. 379 (6564): 445–9. Bibcode:1996Natur.379..445L. doi:10.1038/379445a0. hdl:11858/00-001M-0000-0012-CBFE-2. PMID 8559248. S2CID 4364656.
Modlin, I. M.; Oberg, K.; Chung, D. C.; Jensen, R. T.; De Herder, W. W.; Thakker, R. V.; Caplin, M.; Delle Fave, G.; Kaltsas, G. A.; Krenning, E. P.; Moss, S. F.; Nilsson, O.; Rindi, G.; Salazar, R.; Ruszniewski, P.; Sundin, A. (2008). "Gastroenteropancreatic neuroendocrine tumours". The Lancet Oncology. 9 (1): 61–72. doi:10.1016/S1470-2045(07)70410-2. PMID 18177818. S2CID 46127116.
Pearce, S. H.; Williamson, C; Kifor, O; Bai, M; Coulthard, M. G.; Davies, M; Lewis-Barned, N; McCredie, D; Powell, H; Kendall-Taylor, P; Brown, E. M.; Thakker, R. V. (1996). "A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor". The New England Journal of Medicine. 335 (15): 1115–22. doi:10.1056/NEJM199610103351505. PMID 8813042.
Carpten, J. D.; Robbins, C. M.; Villablanca, A; Forsberg, L; Presciuttini, S; Bailey-Wilson, J; Simonds, W. F.; Gillanders, E. M.; Kennedy, A. M.; Chen, J. D.; Agarwal, S. K.; Sood, R; Jones, M. P.; Moses, T. Y.; Haven, C; Petillo, D; Leotlela, P. D.; Harding, B; Cameron, D; Pannett, A. A.; Höög, A; Heath h, 3rd; James-Newton, L. A.; Robinson, B; Zarbo, R. J.; Cavaco, B. M.; Wassif, W; Perrier, N. D.; Rosen, I. B.; et al. (2002). "HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome". Nature Genetics. 32 (4): 676–80. doi:10.1038/ng1048. PMID 12434154. S2CID 23713328.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Brandi, M. L.; Gagel, R. F.; Angeli, A; Bilezikian, J. P.; Beck-Peccoz, P; Bordi, C; Conte-Devolx, B; Falchetti, A; Gheri, R. G.; Libroia, A; Lips, C. J.; Lombardi, G; Mannelli, M; Pacini, F; Ponder, B. A.; Raue, F; Skogseid, B; Tamburrano, G; Thakker, R. V.; Thompson, N. W.; Tomassetti, P; Tonelli, F; Wells Jr, S. A.; Marx, S. J. (2001). "Guidelines for diagnosis and therapy of MEN type 1 and type 2". The Journal of Clinical Endocrinology and Metabolism. 86 (12): 5658–71. doi:10.1210/jcem.86.12.8070. PMID 11739416.
Lemmens, I; Van De Ven, W. J.; Kas, K; Zhang, C. X.; Giraud, S; Wautot, V; Buisson, N; De Witte, K; Salandre, J; Lenoir, G; Pugeat, M; Calender, A; Parente, F; Quincey, D; Gaudray, P; De Wit, M. J.; Lips, C. J.; Höppener, J. W.; Khodaei, S; Grant, A. L.; Weber, G; Kytölä, S; Teh, B. T.; Farnebo, F; Thakker, R. V. (1997). "Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1". Human Molecular Genetics. 6 (7): 1177–83. doi:10.1093/hmg/6.7.1177. PMID 9215690.

gdst.net (Global: low place; English: low place)

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"Oxford High School GDST School Governors". Archived from the original on 4 July 2014.

handle.net (Global: 102^nd place; English: 76^th place)

hdl.handle.net

Lloyd, S. E.; Pearce, S. H.; Fisher, S. E.; Steinmeyer, K; Schwappach, B; Scheinman, S. J.; Harding, B; Bolino, A; Devoto, M; Goodyer, P; Rigden, S. P.; Wrong, O; Jentsch, T. J.; Craig, I. W.; Thakker, R. V. (1996). "A common molecular basis for three inherited kidney stone diseases". Nature. 379 (6564): 445–9. Bibcode:1996Natur.379..445L. doi:10.1038/379445a0. hdl:11858/00-001M-0000-0012-CBFE-2. PMID 8559248. S2CID 4364656.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Lloyd, S. E.; Pearce, S. H.; Fisher, S. E.; Steinmeyer, K; Schwappach, B; Scheinman, S. J.; Harding, B; Bolino, A; Devoto, M; Goodyer, P; Rigden, S. P.; Wrong, O; Jentsch, T. J.; Craig, I. W.; Thakker, R. V. (1996). "A common molecular basis for three inherited kidney stone diseases". Nature. 379 (6564): 445–9. Bibcode:1996Natur.379..445L. doi:10.1038/379445a0. hdl:11858/00-001M-0000-0012-CBFE-2. PMID 8559248. S2CID 4364656.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Holmes, David (2013). "Rajesh Thakker: A man of hidden depths". The Lancet Diabetes & Endocrinology. 1 (4): 274. doi:10.1016/S2213-8587(13)70196-7. PMID 24622412.
Lloyd, S. E.; Pearce, S. H.; Fisher, S. E.; Steinmeyer, K; Schwappach, B; Scheinman, S. J.; Harding, B; Bolino, A; Devoto, M; Goodyer, P; Rigden, S. P.; Wrong, O; Jentsch, T. J.; Craig, I. W.; Thakker, R. V. (1996). "A common molecular basis for three inherited kidney stone diseases". Nature. 379 (6564): 445–9. Bibcode:1996Natur.379..445L. doi:10.1038/379445a0. hdl:11858/00-001M-0000-0012-CBFE-2. PMID 8559248. S2CID 4364656.
Modlin, I. M.; Oberg, K.; Chung, D. C.; Jensen, R. T.; De Herder, W. W.; Thakker, R. V.; Caplin, M.; Delle Fave, G.; Kaltsas, G. A.; Krenning, E. P.; Moss, S. F.; Nilsson, O.; Rindi, G.; Salazar, R.; Ruszniewski, P.; Sundin, A. (2008). "Gastroenteropancreatic neuroendocrine tumours". The Lancet Oncology. 9 (1): 61–72. doi:10.1016/S1470-2045(07)70410-2. PMID 18177818. S2CID 46127116.
Pearce, S. H.; Williamson, C; Kifor, O; Bai, M; Coulthard, M. G.; Davies, M; Lewis-Barned, N; McCredie, D; Powell, H; Kendall-Taylor, P; Brown, E. M.; Thakker, R. V. (1996). "A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor". The New England Journal of Medicine. 335 (15): 1115–22. doi:10.1056/NEJM199610103351505. PMID 8813042.
Carpten, J. D.; Robbins, C. M.; Villablanca, A; Forsberg, L; Presciuttini, S; Bailey-Wilson, J; Simonds, W. F.; Gillanders, E. M.; Kennedy, A. M.; Chen, J. D.; Agarwal, S. K.; Sood, R; Jones, M. P.; Moses, T. Y.; Haven, C; Petillo, D; Leotlela, P. D.; Harding, B; Cameron, D; Pannett, A. A.; Höög, A; Heath h, 3rd; James-Newton, L. A.; Robinson, B; Zarbo, R. J.; Cavaco, B. M.; Wassif, W; Perrier, N. D.; Rosen, I. B.; et al. (2002). "HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome". Nature Genetics. 32 (4): 676–80. doi:10.1038/ng1048. PMID 12434154. S2CID 23713328.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Brandi, M. L.; Gagel, R. F.; Angeli, A; Bilezikian, J. P.; Beck-Peccoz, P; Bordi, C; Conte-Devolx, B; Falchetti, A; Gheri, R. G.; Libroia, A; Lips, C. J.; Lombardi, G; Mannelli, M; Pacini, F; Ponder, B. A.; Raue, F; Skogseid, B; Tamburrano, G; Thakker, R. V.; Thompson, N. W.; Tomassetti, P; Tonelli, F; Wells Jr, S. A.; Marx, S. J. (2001). "Guidelines for diagnosis and therapy of MEN type 1 and type 2". The Journal of Clinical Endocrinology and Metabolism. 86 (12): 5658–71. doi:10.1210/jcem.86.12.8070. PMID 11739416.
Lemmens, I; Van De Ven, W. J.; Kas, K; Zhang, C. X.; Giraud, S; Wautot, V; Buisson, N; De Witte, K; Salandre, J; Lenoir, G; Pugeat, M; Calender, A; Parente, F; Quincey, D; Gaudray, P; De Wit, M. J.; Lips, C. J.; Höppener, J. W.; Khodaei, S; Grant, A. L.; Weber, G; Kytölä, S; Teh, B. T.; Farnebo, F; Thakker, R. V. (1997). "Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1". Human Molecular Genetics. 6 (7): 1177–83. doi:10.1093/hmg/6.7.1177. PMID 9215690.

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"EME Programme appoint new Chair of Funding Board". www.nihr.ac.uk. Archived from the original on 17 September 2016.

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ORCID 0000-0002-1438-3220

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Bowl, Michael Richard (2003). Molecular genetics of hypoparathyroid disorders (DPhil thesis). University of Oxford. EThOS uk.bl.ethos.275359.
Bradley, Karin J. (2006). Molecular genetics of the hyperparathyroidism-jaw tumour syndrome (DPhil thesis). University of Oxford.
Leotlela, Poloko D. (2003). Molecular genetics of multiple endocrine neoplasia type 1 and related disorders (DPhil thesis). University of Oxford.
Loureiro de Lemos, Manuel C. (2007). Genetic and phenotypic studies of the multiple endocrine neoplasia type 1 syndrome (DPhil thesis). University of Oxford. EThOS uk.bl.ethos.445777.
Jeyabalan, Jeshmi (2008). Role of sedlin in spondyloepiphyseal dysplasia tarda (DPhil thesis). University of Oxford. EThOS uk.bl.ethos.496979.
Turner, Jeremy James Osborne (2003). Molecular genetics of renal tubular disorders affecting urate transport (DPhil thesis). University of Oxford.
Wu, Fiona (2014). Dent's disease and the chloride channel, CLC-5 (DPhil thesis). University of Oxford.

some.ox.ac.uk

Professor Rajesh Thakker, Somerville College, University of Oxford

ocdem.ox.ac.uk

Prof Rajesh V Thakker, Oxford Centre for Diabetes, Endocrinology and Metabolism OCDEM

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gtr.rcuk.ac.uk

UK Government research grants awarded to Rajesh Thakker, via Research Councils UK

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"Professor Rajesh Thakker FMedSci FRS". London: The Royal Society. Archived from the original on 5 August 2014.

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Rajesh Thakker publications indexed by the Scopus bibliographic database. (subscription required)

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Lloyd, S. E.; Pearce, S. H.; Fisher, S. E.; Steinmeyer, K; Schwappach, B; Scheinman, S. J.; Harding, B; Bolino, A; Devoto, M; Goodyer, P; Rigden, S. P.; Wrong, O; Jentsch, T. J.; Craig, I. W.; Thakker, R. V. (1996). "A common molecular basis for three inherited kidney stone diseases". Nature. 379 (6564): 445–9. Bibcode:1996Natur.379..445L. doi:10.1038/379445a0. hdl:11858/00-001M-0000-0012-CBFE-2. PMID 8559248. S2CID 4364656.
Modlin, I. M.; Oberg, K.; Chung, D. C.; Jensen, R. T.; De Herder, W. W.; Thakker, R. V.; Caplin, M.; Delle Fave, G.; Kaltsas, G. A.; Krenning, E. P.; Moss, S. F.; Nilsson, O.; Rindi, G.; Salazar, R.; Ruszniewski, P.; Sundin, A. (2008). "Gastroenteropancreatic neuroendocrine tumours". The Lancet Oncology. 9 (1): 61–72. doi:10.1016/S1470-2045(07)70410-2. PMID 18177818. S2CID 46127116.
Carpten, J. D.; Robbins, C. M.; Villablanca, A; Forsberg, L; Presciuttini, S; Bailey-Wilson, J; Simonds, W. F.; Gillanders, E. M.; Kennedy, A. M.; Chen, J. D.; Agarwal, S. K.; Sood, R; Jones, M. P.; Moses, T. Y.; Haven, C; Petillo, D; Leotlela, P. D.; Harding, B; Cameron, D; Pannett, A. A.; Höög, A; Heath h, 3rd; James-Newton, L. A.; Robinson, B; Zarbo, R. J.; Cavaco, B. M.; Wassif, W; Perrier, N. D.; Rosen, I. B.; et al. (2002). "HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome". Nature Genetics. 32 (4): 676–80. doi:10.1038/ng1048. PMID 12434154. S2CID 23713328.{{cite journal}}: CS1 maint: numeric names: authors list (link)

ukwhoswho.com (Global: 1,450^th place; English: 814^th place)

Anon (2014). "Thakker, Prof. Rajesh Vasantlal". Who's Who (online edition via Oxford University Press ed.). A & C Black. doi:10.1093/ww/9780199540884.013.U37302. (Subscription or UK public library membership required.)

web.archive.org (Global: 1^st place; English: 1^st place)

"EME Programme appoint new Chair of Funding Board". www.nihr.ac.uk. Archived from the original on 17 September 2016.
"Professor Rajesh Thakker FMedSci FRS". London: The Royal Society. Archived from the original on 5 August 2014.
"Oxford High School GDST School Governors". Archived from the original on 4 July 2014.

Rajesh Thakker (English Wikipedia)

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