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Yan-Ling Fei

Research Profile

Disorders

Beckwith-Wiedemann Syndrome

Chemicals & Drugs

Physiology

Anatomy

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Publications

TOP 3
Jocelyne M Lew; Yan-Ling Fei; Kirk Aleck; Benjamin J Blencowe; Rosanna Weksberg; Paul D Sadowski
CDKN1C mutation in Wiedemann-Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer.
Rosanna Weksberg; Cheryl Shuman; Oana Caluseriu; Adam Smith; Yan-Ling Fei; Joy Nishikawa; Tracy L Stockley; Lyle Best; David Chitayat; Ann Olney; Elizabeth Ives; Adele Schneider; Timothy H Bestor; Madeline Li; Paul D Sadowski; Jeremy Squire
Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.
Rosanna Weksberg; Joy Nishikawa; Oana Caluseriu; Yan-Ling Fei; Cheryl Shuman; C Wei; Leslie Steele; J Cameron; Adam Smith; I Ambus; Madeline Li; Peter N Ray; Paul D Sadowski; Jeremy Squire
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

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All Publications

2004: Jocelyne M Lew; Yan-Ling Fei; Kirk Aleck; Benjamin J Blencowe; Rosanna Weksberg; Paul D Sadowski
CDKN1C mutation in Wiedemann-Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer.
American journal of medical genetics. Part A 2004;127A(3):268-76.
2002: Rosanna Weksberg; Cheryl Shuman; Oana Caluseriu; Adam Smith; Yan-Ling Fei; Joy Nishikawa; Tracy L Stockley; Lyle Best; David Chitayat; Ann Olney; Elizabeth Ives; Adele Schneider; Timothy H Bestor; Madeline Li; Paul D Sadowski; Jeremy Squire
Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.
Human molecular genetics 2002;11(11):1317-25.
2001: Rosanna Weksberg; Joy Nishikawa; Oana Caluseriu; Yan-Ling Fei; Cheryl Shuman; C Wei; Leslie Steele; J Cameron; Adam Smith; I Ambus; Madeline Li; Peter N Ray; Paul D Sadowski; Jeremy Squire
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
Human molecular genetics 2001;10(26):2989-3000.
2001: Madeline Li; Cheryl Shuman; Yan-Ling Fei; E Cutiongco; H A Bender; C Stevens; Louise Wilkins-Haug; D Day-Salvatore; S L Yong; M T Geraghty; Jeremy Squire; Rosanna Weksberg
GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome.
American journal of medical genetics 2001;102(2):161-8.
2001: Madeline Li; Jeremy Squire; Cheryl Shuman; Yan-Ling Fei; J Atkin; R Pauli; Adam Smith; Joy Nishikawa; David Chitayat; Rosanna Weksberg
Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
Genomics 2001;74(3):370-6.
2000: Jeremy A Squire; Madeline Li; S Perlikowski; Yan-Ling Fei; Jane Bayani; Z M Zhang; Rosanna Weksberg
Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
Genomics 2000;65(3):234-42.