Gösta Holmgren

Overview

Best Publications

• Identification of the gene responsible for Best macular dystrophy

  K. Petrukhin;M. J. Koisti;B. Bakall;Wen Li

  799
  Citations

• Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis

  G Holmgren;L Steen;O Suhr;B.-G Ericzon

  623
  Citations

• Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP‐met30)

  Gösta Holmgren;Lars Steen;Jan Ekstedt;Carl-Gustav Groth

  459
  Citations

• Coexpression of the sis and myc proto-oncogenes in developing human placenta suggests autocrine control of trophoblast growth

  Anton Scott Goustin;Christer Betsholtz;Susan Pfeifer-Ohlsson;Håkan Persson

  380
  Citations

• A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception

  Elisabet Einarsdottir;Anna Carlsson;Jan Minde;Göran Toolanen

  361
  Citations

• The X-ray crystal structure refinements of normal human transthyretin and the amyloidogenic Val-30→Met variant to 1.7-Å resolution

  Jean A. Hamilton;Larry K. Steinrauf;Bradford C. Braden;Juris Liepnieks

  298
  Citations

• The epidemiology of diabetes in Swedish children 0-14 years--a six-year prospective study.

  G. Dahlquist;L. Blom;G. Holmgren;B. Hägglöf

  287
  Citations

• Malnutrition and gastrointestinal dysfunction as prognostic factors for survival in familial amyloidotic polyneuropathy

  O. Suhr;Å. Danielsson;G. Holmgren;L. Steen

  284
  Citations

• Liver transplantation in familial amyloidotic polyneuropathy : follow-up of the first 20 Swedish patients

  Ole B. Suhr;Gösta Holmgren;Lars Steen;Lars Wikström

  247
  Citations

• Expanded CAG Repeats in Swedish Spinocerebellar Ataxia Type 7 (SCA7) Patients: Effect of CAG Repeat Length on the Clinical Manifestation

  Jenni Johansson;Lars Forsgren;Ola Sandgren;Alexis Brice

  215
  Citations

• Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method.

  K Lindblad;P O Nylander;A De bruyn;D Sourey

  194
  Citations

• Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate.

  G. Holmgren;P. M. P. Costa;C. Andersson;K. Asplund

  190
  Citations

• Oxidative stress is found in amyloid deposits in systemic amyloidosis.

  Yukio Ando;Nils Nyhlin;Ole Suhr;Gösta Holmgren

  186
  Citations

• Epidemiology of motor neuron disease in northern Sweden.

  L Forsgren;B G Almay;G Holmgren;S Wall

  171
  Citations

• Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26.

  Marie Burstedt;Ola Sandgren;Gösta Holmgren;Kristina Forsman-Semb

  168
  Citations

• Familial Amyloidotic Polyneuropathy in Sweden: Geographical Distribution, Age of Onset, and Prevalence

  Alda Sousa;Rune Andersson;Ulf Drugge;Gösta Holmgren

  163
  Citations

• A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)

  Carina K. Mårdh;Birgitta Bäckman;Gösta Holmgren;Jan C.-C. Hu

  159
  Citations

• An expanded CAG repeat sequence in spinocerebellar ataxia type 7.

  Kerstin Lindblad;Marja Liisa Savontaus;Giovanni Stevanin;Monica Holmberg

  145
  Citations

• Severe mental retardation in children in a northern Swedish county.

  H K Blomquist;K H Gustavson;G Holmgren

  144
  Citations

• Hereditary transthyretin amyloidosis from a Scandinavian perspective

  O. B. Suhr;I. Hastrup Svendsen;R. Andersson;Å. Danielsson

  143
  Citations