Farida Latif

Overview

Best Publications

• Identification of the von Hippel-Lindau disease tumor suppressor gene.

  F Latif;K Tory;J Gnarra;M Yao

  3511
  Citations

• Mutations of the VHL tumour suppressor gene in renal carcinoma

  J.R. Gnarra;K. Tory;Y. Weng;L. Schmidt

  2045
  Citations

• Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

  J G Herman;F Latif;Y Weng;M I Lerman

  1949
  Citations

• Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

  Dewi Astuti;Farida Latif;Ashraf Dallol;Patricia L.M. Dahia

  1259
  Citations

• Epigenetic Inactivation of RASSF1A in Lung and Breast Cancers and Malignant Phenotype Suppression

  David G. Burbee;Eva Forgacs;Sabine Zöchbauer-Müller;Latha Shivakumar

  1035
  Citations

• Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

  Chen F;Kishida T;Yao M;Hustad T

  648
  Citations

• High Resolution Chromosome 3p Allelotyping of Human Lung Cancer and Preneoplastic/Preinvasive Bronchial Epithelium Reveals Multiple, Discontinuous Sites of 3p Allele Loss and Three Regions of Frequent Breakpoints

  Ignacio I. Wistuba;Carmen Behrens;Arvind K. Virmani;Gina Mele

  590
  Citations

• Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.

  Angelo Agathanggelou;Sofia Honorio;Donia P Macartney;Alonso Martinez

  541
  Citations

• Role of the Ras-association domain family 1 tumor suppressor gene in human cancers.

  Angelo Agathanggelou;Wendy N. Cooper;Farida Latif

  537
  Citations

• Germline SDHB Mutations and Familial Renal Cell Carcinoma

  Christopher Ricketts;Emma R. Woodward;Pip Killick;Mark R. Morris

  399
  Citations

• Germline SDHD mutation in familial phaeochromocytoma

  Dewi Astuti;Fiona Douglas;Thomas W J Lennard;Irene A. Aligianis

  303
  Citations

• SLIT2, a Human Homologue of the Drosophila Slit2 Gene, Has Tumor Suppressor Activity and Is Frequently Inactivated in Lung and Breast Cancers

  Ashraf Dallol;Nancy Fernandes Da Silva;Paolo Viacava;John D. Minna

  287
  Citations

• The Role of RASSF1A Methylation in Cancer

  Luke B. Hesson;Wendy N. Cooper;Farida Latif

  287
  Citations

• Epigenetic Inactivation of the RASSF1A 3p21.3 Tumor Suppressor Gene in Both Clear Cell and Papillary Renal Cell Carcinoma

  Catherine Morrissey;Alonso Martinez;Malgorzata Zatyka;Angelo Agathanggelou

  277
  Citations

• Functional Properties of a New Voltage-dependent Calcium Channel α2δ Auxiliary Subunit Gene (CACNA2D2)

  Boning Gao;Yoshitaka Sekido;Anton Maximov;Mohamad Saad

  268
  Citations

• Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

  Dewi Astuti;Mark R Morris;Mark R Morris;Wendy N Cooper;Raymond H J Staals

  263
  Citations

• Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma.

  Mark Morris;Christopher Ricketts;Dean Gentle;Fiona McRonald

  240
  Citations

• Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

  Carol Hardy;Farhat Khanim;Rosarelis Torres;Rosarelis Torres;Martin Scott-Brown

  238
  Citations

• The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation

  Volker Endris;Birgit Wogatzky;Uwe Leimer;Dusan Bartsch

  238
  Citations

• Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.

  Hiltrud Brauch;Takeshi Kishida;Damjan Glavac;Fan Chen

  237
  Citations