Dr. Bin Tean Teh
National Cancer Center, USA
Email: Teh.bin.tean@singhealth.com.sg
Qualifications
Group Director, Translational
Research, Singapore
Principal Investigator, National
Cancer Centre, Singapore
Professor, Duke-NUS Graduate Medical
School, Singapore
Professor, Center for Cancer Genomics
and Computational Biology, Singapore
Head, Laboratory of Cancer Genetics,
Singapore
Co-Head, Kidney Cancer Research
Program, Singapore
Publications (Selected)
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Larsson C, Calender A, Grimmond S,
Giraud S, Hayward N, Teh BT, Farnebo F. Molecular tools for presymptomatic
testing in multiple endocrine neoplasia type 1.J Int Med 238: 239–244, 1995
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Teh BT, Silburn P, Linblad K, Betz R,
Boyle R, Schalling M, Larsson C. Familial periodic cerebellar ataxia without
myokimia maps to a 19-cM region on chromosome 19p13.Am J Hum Genet
56: 1443–1449, 1995
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Cuneo RC, Hickman PE, Wallace JD, Teh
BT, Ward G, Veldhuis JD, Walters MJ. Altered endogenous growth hormone
secretory kinetics and diurnal GH-binding protein profiles in adults with
chronic liver disease.Clin Endocrinol 43: 265–275, 1995
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Teh BT, Hansen J, Svensson PJ, Hartley
L. Bilateral recurrent phaeochromocytoma associated with a growth
hormone-secreting pituitary tumour.Br J Surg 83: 1132, 1996
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Heath H 3rd, Odelberg S, Jackson CE,
Teh BT, Hayward N, Larsson C, Buist NR, Krapcho KJ, Hung BC, Capuano IV,
Garrett JE, Leppert MF. Clustered inactivating mutations and benign
polymorphisms of the calcium receptor gene in familial benign hypocalciuric
hypercalcemia suggest receptor functional domains.J Clin Endocrinol Metab
81: 1312–1317, 1996
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Grimmond SM, Teh BT, Hii SI, Cardinal
J, Walters M, Epstein M, Edwards M, Hockey A, Pullan PT, Perry-Keene D, Boyages
S, Cameron D, Hayward NK. Predictive diagnosis of multiple endocrine neoplasia
(MEN1) in four Australian kindreds.Aust NZ J Med 26: 27–32, 1996
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Grimmond SM, Palmer JM, Walters MK,
Scott C, Nancarrow DJ, Teh BT, Elmes C, Pyke C, Khoo S, Bennett I, Wetzig N,
Hayward NK. Confirmation of a susceptibility locus on chromosome 13 in
Australian breast cancer families.Hum Genet 98: 80–85, 1996
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Teh BT, McArdle J, Parameswaran V,
David R, Larsson C, Shepherd J. Sporadic primary hyperparathyroidism in the
setting of multiple endocrine neoplasia type 1.Arch Surg 131: 1230–1232, 1996
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Dotzenrath C, Teh BT, Farnebo F,
Cupisti K, Svensson A, Toell A, Goretzki P, Larsson C. Allelic loss of the
retinoblastoma tumor suppressor gene: a marker for aggressive parathyroid
tumors? J Clin Endocrinol Metab 81: 3194–3196,
1996
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Teh BT, Farnebo F, Kristoffersson U,
Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath H 3rd, Cameron D,
Larsson C. Autosomal dominant primary hyperparathyroidism-jaw tumour syndrome
associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32
and loss of the wild-type allele in renal hamartomas.J Clin Endocrinol Metab
81: 4204–4211, 1996
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Sullivan AA, Teh BT, Jeavons S,
Schalling M, Silburn P, Larsson C, Boyle R. Cerebral autosomal dominant
arteriopathy with subcortical infarcts and leucoencephalopathy. J Clin
Neuroscience 4: 176–180, 1997
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Teh BT, Sullivan AA, Farnebo F, Zander
C, Li FY, Strachan N, Schalling M, Larsson C, Sandstrom P. Oculopharyngeal
muscular dystrophy (OPMD)--case report and genetic studies of an Australian
kindred.Clin Genet 51: 52–55, 1997
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Stock J, Warth M, Teh BT, Coderre JA,
Overdorf JH, Baumann G, Hintz RL, Hartman ML, Seizinger BR, Larsson C, Aronin
N. A kindred with a variant of multiple endocrine neoplasia type 1
demonstrating frequent expression of pituitary tumors but not linked to
multiple endocrine neoplasia type 1 locus at chromosome region 11q13.J Clin
Endocrinol Metab 82: 486–492, 1997
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Teh BT, McArdle J, Chan SP, Mennon J,
Hartley L, Pullen P, Ho J, Khir A, Wilkinson S, Larsson C, Cameron D, Shepherd
J. Clinicopathologic studies of thymic carcinoids in multiple endocrine
neoplasia type 1.Medicine 76: 21–29, 1997
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Teh BT, Birrell G, Farrell A, Leonard
H, Walters M, Palmer J, Ramsay J, Schlect D, Furnival C, Lavin M, Bennett I,
Hayward N. Malignant breast cancer in six patients with neurofibromatosis type
1. Breast 6: 155–160, 1997
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Lassam NJ, Lin Z, Shennan MG,
Courseaux A, Teh BT, Gaudray P, Larsson C. Fine mapping of the MLK-3 gene
within 11q13 and its exclusion as the MEN1 susceptibility gene. Hum Genet
99: 776–780, 1997
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Farnebo F, Teh BT, Dotzenrath C,
Wassif WS, Svensson A, White I, Betz R, Goretzki P, Sandelin K, Farnebo LO,
Larsson C. Differential loss of heterozygosity in familial, sporadic and uremic
hyperparathyroidism.Hum Genet 99: 342–349, 1997