Neil V. Morgan

Overview

Best Publications

• Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia

  Richard Trembath;J R Thomson;Rajiv Machado;N Morgan

  872
  Citations

• Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family.

  Jennifer R Thomson;Rajiv D Machado;Michael W Pauciulo;Neil V Morgan

  849
  Citations

• BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

  Rajiv D Machado;Michael W. Pauciulo;Jennifer R. Thomson;Kirk B. Lane

  637
  Citations

• HIF activation identifies early lesions in VHL kidneys: Evidence for site-specific tumor suppressor function in the nephron

  Stefano J Mandriota;Kevin J Turner;David R Davies;Paul G Murray

  627
  Citations

• PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

  Neil V Morgan;Shawn K Westaway;Jenny E V Morton;Allison Gregory

  582
  Citations

• Constitutive Activation of Hypoxia-inducible Genes Related to Overexpression of Hypoxia-inducible Factor-1α in Clear Cell Renal Carcinomas

  Michael S. Wiesener;Philine M. Münchenhagen;Irina Berger;Neil V. Morgan

  461
  Citations

• Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

  P Gissen;P Gissen;C A Johnson;N Morgan;J M Stapelbroek

  359
  Citations

• The transmembrane protein meckelin ( MKS3 ) is mutated in Meckel-Gruber syndrome and the wpk rat

  Ursula M Smith;Mark Consugar;Louise J Tee;Brandy M McKee

  332
  Citations

• Association of complementation group and mutation type with clinical outcome in Fanconi anemia

  Laurence Faivre;Philippe Guardiola;Cathryn Lewis;Inderjeet Dokal

  308
  Citations

• The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity

  Rune Busk Damgaard;Jennifer A. Walker;Paola Marco-Casanova;Neil V. Morgan

  301
  Citations

• Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene.

  Johan P. de Winter;Carola G.M. van Berkel;Martin A. Rooimans

  284
  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

• Positional cloning of the Fanconi anaemia group A gene

  Sinoula Apostolou;Scott A. Whitmore;Joanna Crawford;Gregory Lennon

  269
  Citations

• STAT2 deficiency and susceptibility to viral illness in humans

  Sophie Hambleton;Stephen Goodbourn;Dan F. Young;Paul Dickinson

  264
  Citations

• Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)

  M. A. Kurian;N. V. Morgan;L. MacPherson;K. Foster

  261
  Citations

• Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

  Manju A. Kurian;Juan Zhen;Shu-Yuan Cheng;Yan Li

  253
  Citations

• Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

  Irene A Aligianis;Colin A Johnson;Paul Gissen;Dongrong Chen

  251
  Citations

• Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism

  Quinten Waisfisz;Neil V. Morgan;Maria Savino;Johan P. de Winter

  247
  Citations

• Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency

  Alexandre Bolze;Minji Byun;David McDonald;Neil V. Morgan

  219
  Citations

• Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

  Neil V. Morgan;Mark R. Morris;Hakan Cangul;Hakan Cangul;Diane Gleeson

  208
  Citations