All Stories

  1. STK11 Gene Analysis Reveals a Significant Number of Splice Mutations in Chinese PJS Patients

    Article • Cancer Genetics, November 2018, Elsevier

    Dr Zi-Ye ZHAO

  2. Adenoma miss rate determined by very shortly repeated colonoscopy

    Article • Medicine, September 2018, Wolters Kluwer Health

    Dr Zi-Ye ZHAO

  3. The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome

    Article • BMC Medical Genetics, August 2018, Springer Science + Business Media

    Dr Zi-Ye ZHAO

  4. A novel STK11 missense mutation (c.346G > T) causing Peutz–Jeghers syndrome in a Chinese male with a negative family history

    Article • Digestive and Liver Disease, June 2018, Elsevier

    Dr Zi-Ye ZHAO

  5. Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl

    Article • BMC Surgery, April 2018, Springer Science + Business Media

    Dr Zi-Ye ZHAO

  6. A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family

    Article • Digestive and Liver Disease, March 2018, Elsevier

    Dr Zi-Ye ZHAO

  7. Drugs for Neuropathic Pain Are Promising in Treating Feed-induced Dystonia in Central Nervous System Disabled Children

    Article • Journal of Pediatric Gastroenterology and Nutrition, January 2018, Wolters Kluwer Health

    Dr Zi-Ye ZHAO

  8. A novel germline mutation (c.A527G) in STK11 gene causes Peutz–Jeghers syndrome in a Chinese girl

    Article • Medicine, December 2017, Wolters Kluwer Health

    Dr Zi-Ye ZHAO

  9. Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient

    Article • BMC Medical Genetics, November 2017, Springer Science + Business Media

    Dr Zi-Ye ZHAO

  10. A 23-Nucleotide Deletion in STK11 Gene Causes Peutz–Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History

    Article • Digestive Diseases and Sciences, October 2017, Springer Science + Business Media

    Dr Zi-Ye ZHAO

  11. Detection and miss rates of autofluorescence imaging of adenomatous and polypoid lesions during colonoscopy: a systematic review and meta-analysis

    Article • Endoscopy International Open, May 2015, Thieme Publishing Group

    Dr Zi-Ye ZHAO