Papers authored by Rajesh Thakker
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2013
Sarah A. Howles,
Mark H. Edwards,
Cyrus Cooper,
Rajesh V. Thakker 
Kidney Stones: A Fetal Origins Hypothesis†
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Paul J. Newey,
Caroline M. Gorvin,
Stephen J. Cleland,
Christian B. Willberg,
Marcus Bridge,
Mohammed Azharuddin,
Russell S. Drummond,
P. Anton van der Merwe,
P. Anton van der Merwe,
Paul Klenerman,
Chas Bountra,
Rajesh V. Thakker
Mutant Prolactin Receptor and Familial Hyperprolactinemia
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Rajesh V. Thakker
Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)
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Jonathan L. Moskowitz,
Sian E. Piret,
Karl Lhotta,
Thomas M. Kitzler,
Adam P. Tashman,
Erin Velez,
Rajesh V. Thakker ,
Peter Kotanko
,
Peter Kotanko
Association between Genotype and Phenotype in Uromodulin-Associated Kidney Disease
Download from cjasn.asnjournals.org
Caroline M. Gorvin,
Martijn J. G. Wilmer,
Sian E. Piret,
Brian Harding,
Lambertus P. van den Heuvel,
L. P. W. J. van den Heuvel,
Oliver Wrong,
Parmjit S. Jat ,
Jonathan D. Lippiat ,
Elena N. Levtchenko,
Rajesh V. Thakker
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,
Jonathan D. Lippiat ,
Elena N. Levtchenko,
Rajesh V. Thakker
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Paul J. Newey,
Newey Pj,
M. Andrew Nesbit,
M. Andrew Nesbit,
Nesbit Ma,
Andrew J. Rimmer,
Rimmer Aj,
Rosie A. Head,
Caroline M. Gorvin,
Head Ra,
Moustafa Attar,
Lorna Gregory,
John A. H. Wass,
Gorvin Cm,
David Buck
and 8 other authors
Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas
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A. Karunaratne,
A. Boyde,
Ct T. Esapa,
J. Hiller,
Nj J. Terrill ,
Sd D. M. Brown,
Rd D. Cox,
Rv V. Thakker ,
Hs S. Gupta
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,
Sd D. M. Brown,
Rd D. Cox,
Rv V. Thakker ,
Hs S. Gupta
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Nellie Y. Loh,
Liz Bentley,
Henrik Dimke,
Sjoerd Verkaart,
Paolo Tammaro,
Caroline M. Gorvin,
Michael J. Stechman,
Bushra N. Ahmad,
Fadil M. Hannan,
Sian E. Piret,
Holly Evans,
Ilaria Bellantuono,
Tertius A. Hough,
William D. Fraser,
Joost G. J. Hoenderop
and 5 other authors
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2012
M. Andrew Nesbit,
M. Andrew Nesbit,
Sa Howles,
Aac Reed,
Ce Thakker,
Aj Rimmer,
Treena Cranston,
Pj Morrison,
Lorna Gregory,
Sj Hunter,
Nigel Rust,
Una Graham,
Fm Hannan,
Michael P. Whyte,
Gil Mcvean
and 2 other authors
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3
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