Tom Strachan

Research.com Recognitions

• 2006 - Fellow of the Royal Society of Edinburgh

Overview

Best Publications

• Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family

  Li Qy;Newbury-Ecob Ra;Newbury-Ecob Ra;Terrett Ja;Wilson Di

  1052
  Citations

• Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

  A. Sakuntabhai;V. Ruiz-Perez;S. Carter;N. Jacobsen

  964
  Citations

• Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

  Mayada Tassabehji;Andrew P. Read;Valerie E. Newton;Rodney Harris

  819
  Citations

• A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

  R Bashir;S Britton;T Strachan;S Keers

  796
  Citations

• Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

  Edgar A. Otto;Bernhard Schermer;Tomoko Obara;John F. O'Toole

  720
  Citations

• NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome.

  Emma T Tonkin;Tzu-Jou Wang;Steven Lisgo;Michael J Bamshad

  719
  Citations

• The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome

  Mark Clement-Jones;Simone Schiller;Ercole Rao;Rüdiger J. Blaschke

  540
  Citations

• Downregulation of NANOG induces differentiation of human embryonic stem cells to extraembryonic lineages.

  Louise Hyslop;Miodrag Stojkovic;Lyle Armstrong;Theresia Walter

  522
  Citations

• Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

  W.H.I. McLean;E.L. Rugg;D.P. Lunny;S.M. Morley

  431
  Citations

• Hailey–Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump

  Ralf Sudbrak;Joanna Brown;Carol Dobson-Stone;Simon Carter

  386
  Citations

• SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

  N.A Hanley;D.M Hagan;M Clement-Jones;S.G Ball

  356
  Citations

• Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

  David Morgan;Lee Turnpenny;Judith Goodship;Weilie Dai

  340
  Citations

• An Autogeneic Feeder Cell System That Efficiently Supports Growth of Undifferentiated Human Embryonic Stem Cells

  Petra Stojkovic;Majlinda Lako;Rebecca Stewart;Stefan Przyborski

  331
  Citations

• A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

  Alison J. Ross;Victor Ruiz-Perez;Yiming Wang;Donna Marie Hagan

  328
  Citations

• Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.

  May Tassabehji;Andrew P. Read;Valerie E. Newton;Michael Patton

  284
  Citations

• Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.

  D. G R Evans;L. Trueman;A. Wallace;S. Collins

  262
  Citations

• A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy Maps to Chromosome 2p

  R. Bashir;T. Strachan;S. Keers;A. Stephenson

  257
  Citations

• Autosomal dominant sacral agenesis: Currarino syndrome

  Sally Ann Lynch;Yiming Wang;T Strachan;John Burn

  252
  Citations

• Derivation of human embryonic stem cells from day-8 blastocysts recovered after three-step in vitro culture.

  Miodrag Stojkovic;Majlinda Lako;Petra Stojkovic;Rebecca Stewart

  249
  Citations

• A genetic study oftype2neurofibromatosi s in theUnitedKingdom. I.Prevalence, mutation rate,fitness, andconfirmation ofmaternal transmission effect on severity

  D G R Evans;SM Huson;D Donnai;W Neary

  0
  Citations