Hou JW, Wang TR (1997): Primed in situ (PRINS) labeling for rapid detection of numerical and structural chromosome anomalies. J Formos Med Assoc 96(1): 46-50.
Hou JW, Wang JK, Wang TR (1997): Microdeletion of chromosomal region 7q11.23 in Williams syndrome. J Formos Med Assoc 96(2): 137-140.
Hou JW, Wang PJ, Wang TR (1997): Angelman syndrome assessed by neurological and molecular cytogenetic investigations. Pediatr Neurol 16(1):17-22.
Lu FL, *Hou JW, Tsai WS, Teng RJ, Tsou Yau KI, Wang TR (1997): Tricho-rhino-phalangeal syndrome type II associated with epiglottic aplasia and congenital nephrotic syndrome. J Formos Med Assoc 96(3): 217-221(corresponding author).
Hou JW, Wang TR (1997): Differentiation of Fanconi anemia from aplastic anemia by chromosomal breakage test. Acta Paediatr Sin 38:121-126.
Jeng SF, Liao HF, Lai JS, Hou JW (1997): Optimization of walking in children. Med Sci Sports Exerc 29:370-376.
Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR (1997): CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. J Formos Med Assoc 96(6):419-423.
Hsu HL, Hsiao PH, *Hou JW, Tsai WY, Wang TR (1997): Partial DiGeorge anomaly associated with 10p deletion. J Formos Med Assoc 96(12):996-999 (corresponding author)
Hou JW, Wang TR (1998): Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan. J Eur Pediatr 157:122-127.
Lin JH, *Hou JW, Lin KH, Wang TR (1998): Jacobsen syndrome with myelodysplastic changes of hemopoietic cells in distal 11q. Am J Med Genet 75:341-344 (corresponding author).
Hou JW, Wang TR, Chuang SM (1998): An epidemiological and etiological study of children with intellectual disability in Taiwan. J Intell Disabil Research 42:137-143.
Lu CY, Teng RJ, Hou JW, Cheng TJ (1998): Bifid tongue associated with midline cleft palate, mandible, cervical vertebral and linea alba. Eur J Pediatr 157:86.
Hou JW, Wang JK, Wang TR (1998): FISH analysis in both classical and atypical cases of Williams-Beuren syndrome. Acta Paediatr Sin 39:398-403.
Hou JW, Wang TR(1999):Extreme Poland anomaly associated with congenital diaphragmatic pernia. Eur J Pediatr 158: 433-434.
Lin SC, Hu FR, Hou JW, et al. (1999): Corneal opacity and congenital glaucoma associated with massive heparan sulfaturia. Acta Paediatr Sin 40:49-52.
Hou JW, Tsai WY, Wang TR (1999): Detection of KAL-1 gene deletion with fluorescence in situ hybridization. J Formos Med Assoc 98: 448-451.
Hsieh YC, *Hou JW (1999): Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect. Am J Med Genet 86; 278-281. (corresponding author).
Wang SM, Hou JW, Lin JL (2006): A retrospective epidemiologic and etiological study of metabolic disorders in children with cardiomyopathies. Acta Paediatr Tw 47: 83-87. (Corresponding author)
Hou JW (2006): Chromosome 10q24.3-qter deletion associated with left-sided first branchial arch defect, diaphragmatic eventration, and duplicated renal pelvis. Am J Med Genet 140A:2241-2244.
Hou JW (2006): Double aneuploidy: trisomy 18 and XXY in a boy. Chang Gung Med J 29 (4 Suppl): 6-12.
Hou JW (2006): Atlantoaxial subluxation with recurrent consciousness disturbance in a boy of Lesch-Nyhan syndrome. Acta Paediatr 95:1500-1504.
Chen RL, Hou JW, Chang PY, et al. (2007): Matched unrelated bone marrow transplantation without splenectomy for a child with Gaucher disease caused by homozygosity of the L444P mutation, who also suffered from schizencephaly. J Pediatr Hematolo/Oncol 29(1): 57-59.
Sato D, Shimokawa O, Harada N, Olsen OE, Hou JW, et al. (2007): Congenital arhinia: Molecular-genetic analysis of five patients. Am J Med Genet 143A(6):546-552.
侯家瑋(2007): 生長激素於兒科疾病治療之新應用。台北市醫師公會會刊 (Journal of Taipei Medical Association)。51(6):42-46.(中文)
Hsu HF, Hou JW (2007): Variable expressivity in Patau syndrome in not all related to trisomy 13 mosaicism. Am J Med Genet (Corresponding author) 143A(15):1739-1748.
Huang JJ, Hou JW, TanYC, Chen KT, Lo LJ, Chen YR (2007): Van der Woude syndrome: Clinical presentation in 64 patients. Cleft Plate-Craniofac J 44(6): 649-652.
Shaw SW, Chen CP, Cheng PJ, Wang TH, Hou JW, Lin CT, Chang SD, Hwa HL, Lin JL, Chao AS, Soong YK, Hsieh FJ (2008): Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome. J Hum Genet 53(2):136-143.
Hou JW (2008): Rapidly progressive scoliosis after successful treatment for osteopenia in Costello syndrome. Am J Med Genet 2008; 146A(3):393-396.
Hannibal MC, Buckingham KJ, Ng SB, Ming JE, Hou JW, et al (2011): Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome. Am J Med Genet Jun 10 [Epub ahead of print]
INTERNATIONAL CONFERENCE PAPERS:
Hou JW, Wu MH, Lue HC (1990): Left ventricular function in beta-thalassemia major by echocardiography. 5th International Symposium of the International College of Pediatrics, April 1-5, 1990. Taipei, Taiwan.
Hou JW, Wang TR, Tsai MH (1990): Study of the gene locus of human ornithine transcarbamylase by restriction fragment length polymorphism in normal Chinese. 5th International Symposium of the International College of Pediatrics, April 1-5, 1990, Taipei, Taiwan.
Lin SJ, Hu SC, Hsu SF, Hou JW, Chio PC, Chao MC, Wang TR (1990): Growth study in Chinese children with Down syndrome in Taiwan: 1 month to 18 years of age. 41st Annual Meeting of the American Society of Human Genetics, October 16-20, 1990, Cincinnati, USA.
Hyland KM, Wydner KL, Hou JW (1991): Use of in situ hybridization in determining the origin of a fragment in a Turner mosaic. 8th International Congress of Human genetics, October 6-11, 1991, Washington D.C., U.S.A.
Wang TR, Hwu WL, Hou JW (1992): Current status of detecting fragile-X syndrome using molecular biology techniques at the National Taiwan University Hospital. In: 1992 San Diego Conference on Nucleic acids: Genetic Recognition.
Hou JW (2001): Clinical and genetic criteria in Taiwan. 2nd Organizational Meeting for International Genetic Epidemiology of Oral Clefts, April 9&10, 2001, Singapore. (Invited Speaker)
Hou JW (2001): Neonatal progeroid disorders: more than one disease. 10th International Congress of Human Genetics, May 14-19, 2001, Vienna, Austria.
Hou JW, Lee TH (2002): Genetic factors in young patients with stroke in Taiwan. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 475.]
Wang SM, Hou JW, Lin J (2002): Treatment experience of neonatal hyperammonemia. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 412.]
Lin J, Wang S, Hou JW (2002): Evaluating clinical efficacy and safety of palmidronate in patients with osteogenesis imperfecta. American Society of Human Genetics, 52nd Annual Meeting, Oct 15-19, 2002, Baltimore, USA. [Am J Hum Genet 71 (suppl): 255.]
Hou JW (2003): No evidence of HESX1 mutation in five cases of septo-optic dysplasia with variable phenotype, including metabolic cardiomyopathy and further brain anomalies. European Human Genetics Conference 2003, May 3-6 Birmingham, England.
Hou JW (2003): Wolf-Hirschhorn syndrome: clinical and molecular cytogenetic studies in Taiwan. American Society of Human Genetics, 53rd Annual Meeting, Nov. 14-8, 2003, Los Angeles, USA. [Am J Hum Genet 73 (suppl): 273.]
Hou JW (2004): Growth hormone deficiency associated with chronic diseases. 15th Symposium on Growth Hormone and Endocrinology, Apr. 1-3, 2004, Malta.
Hou JW (2004): Issues and management of GHD in Taiwan. North Asia Paediatric Endocrinology Workshop, July 10-11, Guilin, China. (Invited Speaker)
Hou JW (2004): Effects of coenzyme Q10 and growth hormone on psychomotor in children with Prader-Willi syndrome. The 3rd Biennial Scientific Meeting Asia Pacific Paediatric Endocrine Society, Sept 24-26, Kobe, Japan
Hou JW (2004): American Society of Human Genetics, 54th Annual Meeting, Dec. 26-30, 2004, Toronto, Canada. [Am J Hum Genet 74 (suppl):]
Hou JW (2005): Long-term follow-up of patients with Kabuki syndrome in Taiwan. European Human Genetics Conference, May 7-10, 2005, Prague, Czech Republic.
Hou JW (2006): Clinical Approach to Carnitine Deficiency Disorders. 4th International Huaxia Congress of Endocrinology, Dec 15-18, 2006, Hong Kong. (Invited Speaker)
Hou JW (2007): MPS diseases. 10th Annual Asia LSD Symposium, Dec 9-12, 2007, Kuala Lumpur, Malaysia. (Invited Speaker)
Tato L, Chatelain P, Duk-Hee K, Bashnina E, Sultanova L, Hou JW, Olivier C, Saunders H, Clayton P, and the PREDICT investigators (2008): Baseline auxological and biochemical characteristics of prepubertal growth hormone deficient (GHD) versus Turner syndrome (TS) children in the PREDICT study. The Endocrine Society’s 90th Annual Meeting, June 15-18, 2008, San Francisco, USA.
Hou JW (2010): Maple syrup urine disease and infantile epilepsy. International Symposium on Epilepsy in Neurometabolic Diseases. The 13th Annual Meeting of Infantile Seizure Society. Mar 26-28, Taipei, Taiwan (Invited Speaker)
Feng WK, Hung KL, Hou JW (2010): Epilesies in MELAS syndrome. International Symposium on Epilepsy in Neurometabolic Diseases. The 13th Annual Meeting of Infantile Seizure Society. Mar 26-28, Taipei
Hou JW (2010): Identification and carrier-frequency detection of maple syrup urine disease in the aboriginal tribes of north Taiwan: different gene preference from Asian Society for Pediatric Research. Apr 15-18, Taipei