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Timothy H.J. Goodship

Timothy H.J. Goodship

D-Index & Metrics

Biology and Biochemistry

D-Index
72
Citations
20842
World Ranking
6230
National Ranking
477

Medicine

D-Index
72
Citations
20879
World Ranking
19806
National Ranking
1780

Overview

Timothy H.J. Goodship is affiliated with Newcastle University in the United Kingdom. Their work is situated within an academic environment known for research and education.

No records of recent papers, frequent coauthors, or common publication venues are available, which limits insight into the detailed aspects of their scholarly output or collaborations.

Similarly, there is no available data on book publications, main fields of study, subfields of study, or main topics of work related to Goodship.

There are no recorded awards or honors attributed to this researcher at this time.

The absence of these data points conveys that specific details on Timothy H.J. Goodship's research focus, contributions, and recognition have not been documented or are not accessible through the current sources.

Best Publications

  • Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome

    C.M. Legendre;C. Licht;P. Muus;L.A. Greenbaum

  • Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

    Marina Noris;Jessica Caprioli;Elena Bresin;Chiara Mossali

  • Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

    Timothy H.J. Goodship;H. Terence Cook;Fadi Fakhouri;Fernando C. Fervenza

  • Genetic studies into inherited and sporadic hemolytic uremic syndrome

    Paul Warwicker;Timothy H.J. Goodship;Timothy H.J. Goodship;Timothy H.J. Goodship;Rosemary L. Donne;Rosemary L. Donne;Rosemary L. Donne;Yves Pirson;Yves Pirson;Yves Pirson

  • A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.

    Anne E Hughes;Nick Orr;Hossein Esfandiary;Martha Diaz-Torres

  • Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

    Anna Richards;Elizabeth J Kemp;M Kathryn Liszewski;Judith A Goodship

  • Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome

    David Kavanagh;Elizabeth J. Kemp;Elizabeth Mayland;Robin J. Winney

  • Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies

    Christoph Licht;Larry A. Greenbaum;Petra Muus;Sunil Babu

  • Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

    Elena Bresin;Erica Rurali;Jessica Caprioli;Pilar Sanchez-Corral

  • Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

    Peter F Zipfel;Matthew Edey;Stefan Heinen;Mihály Józsi

  • A randomized multicenter clinical trial comparing isosmolar Icodextrin with hyperosmolar glucose solutions in CAPD

    Chandra D. Mistry;Chandra D. Mistry;Ram Gokal;Ram Gokal;Elizabeth Peers;Elizabeth Peers;C.B. Brown

  • Atypical Hemolytic Uremic Syndrome

    David Kavanagh;Tim H. Goodship;Anna Richards

  • Atypical aHUS: State of the art.

    Carla M. Nester;Thomas Barbour;Santiago Rodriquez de Cordoba;Marie Agnes Dragon-Durey

  • Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort

    Jane E. Salmon;Cara Heuser;Michael Triebwasser;M. Kathryn Liszewski

  • Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

    Iain Moore;Lisa Strain;Isabel Pappworth;David Kavanagh

  • Correction of acidosis in hemodialysis decreases whole-body protein degradation.

    K. A. Graham;D. Reaich;S. M. Channon;S. Downie

  • Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.

    C Mark Taylor;Sam Machin;Stephen J Wigmore;Tim H J Goodship

  • Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

    H.-J. Lüdecke;J. Schaper;P. Meinecke;P. Momeni

  • Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background.

    Elena Bresin;Erica Daina;Marina Noris;Federica Castelletti

  • ATYPICAL HEMOLYTIC UREMIC SYNDROME AND C3 GLOMERULOPATHY: CONCLUSIONS FROM A «KIDNEY DISEASE: IMPROVING GLOBAL OUTCOMES» (KDIGO) CONTROVERSIES CONFERENCE

    Timothy H.J. Goodship;H. Terence Cook;Fadi Fakhouri;Fernando C. Fervenza

Frequent Co-Authors

David J. Kavanagh
David J. Kavanagh Queensland University of Technology
Judith A. Goodship
Judith A. Goodship Newcastle University
Marina Noris
Marina Noris Mario Negri Institute for Pharmacological Research
Giuseppe Remuzzi
Giuseppe Remuzzi Mario Negri Institute for Pharmacological Research
Chantal Loirat
Chantal Loirat Grenoble Alpes University
John P. Atkinson
John P. Atkinson Washington University in St. Louis
Peter F. Zipfel
Peter F. Zipfel Friedrich Schiller University Jena
Adrian S. Woolf
Adrian S. Woolf University of Manchester
Santiago Rodríguez de Córdoba
Santiago Rodríguez de Córdoba Spanish National Research Council

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