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Suh-Jen Chen

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TOP 3
Pen-Hua Su; Y-N Su; C-P Chen; Suh-Jen Chen; L-L Lin; Jia-Yuh Chen
Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
Pen-Hua Su; Shun-Fa Yang; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
A polymorphism in the leptin receptor gene at position 223 is associated with growth hormone replacement therapy responsiveness in idiopathic short stature and growth hormone deficiency patients.
Pen-Hua Su; Shun-Fa Yang; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
Study of the leptin levels and its gene polymorphisms in patients with idiopathic short stature and growth hormone deficiency.

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All Publications

2013: Pen-Hua Su; Y-N Su; C-P Chen; Suh-Jen Chen; L-L Lin; Jia-Yuh Chen
Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
Genetics and molecular research : GMR 2013;12(2):1311-7.
2012: Pen-Hua Su; Shun-Fa Yang; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
A polymorphism in the leptin receptor gene at position 223 is associated with growth hormone replacement therapy responsiveness in idiopathic short stature and growth hormone deficiency patients.
European journal of medical genetics 2012;55(12):682-7.
2012: Pen-Hua Su; Shun-Fa Yang; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
Study of the leptin levels and its gene polymorphisms in patients with idiopathic short stature and growth hormone deficiency.
Endocrine 2012;42(1):196-204.
2012: Ching-Hsuan Hu; Yu-Fan Liu; Yan-Yan Ng; Pen-Hua Su; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain.
American journal of medical genetics. Part A 2012;158A(4):726-31.
2012: Pen-Hua Su; Shun-Fa Yang; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen
Study of leptin levels and gene polymorphisms in patients with central precocious puberty.
Pediatric research 2012;71(4 Pt 1):361-7.
2012: Tsung-Hsin Wu; Trang-Tiau Wu; Jia-Yuh Chen; Soo-Cheen Ng; Yan-Yan Ng; Pen-Hua Su; Suh-Jen Chen
Herlyn-Werner-Wunderlich syndrome consisting of uterine didelphys, obstructed hemivagina and ipsilateral renal agenesis in a newborn.
Pediatrics and neonatology 2012;53(1):68-71.
2011: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen
Siblings with deletion 22q13.3 and trisomy 15q26 inherited from a maternally balanced translocation.
Pediatrics and neonatology 2011;52(5):287-9.
2011: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Inn-Chi Lee; Ju-Shan Yu; Teng-Fu Tsao
Interstitial deletions of the short arm of chromosome 4 in a patient with mental retardation and focal seizure.
Pediatrics and neonatology 2011;52(3):165-8.
2011: Chiu-Yueh Hsiao; Shu-Hsing Lee; Suh-Jen Chen; Marcia Van Riper; Shu-Chin Lin
Taiwanese nursing students' perceived knowledge and clinical comfort with genetics.
Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau 2011;43(2):125-32.
2011: Pen-Hua Su; Jia-Yuh Chen; Ju-Shan Yu; Suh-Jen Chen; Shun-Fa Yang
Leptin expression and leptin receptor gene polymorphisms in growth hormone deficiency patients.
Human genetics 2011;129(4):455-62.
2011: Pen-Hua Su; Jia-Yuh Chen; Teng-Fu Tsao; Suh-Jen Chen
De novo interstitial deletion of chromosome 2 (p23p24).
Pediatrics and neonatology 2011;52(1):46-50.
2011: Pen-Hua Su; Ju-Shan Yu; Suh-Jen Chen; Jia-Yuh Chen; Teng-Fu Tsao
Persistent falcine sinus and unilateral renal agenesis in a girl with Sotos syndrome.
Clinical dysmorphology 2011;20(1):42-6.
2010: Fong-Fong Lim; Yan-Yan Ng; Jui-Ming Hu; Suh-Jen Chen; Pen-Hua Su; Jia-Yuh Chen
Ocular findings in a case of trisomy 18 with variant of Dandy-Walker syndrome.
Pediatrics and neonatology 2010;51(5):292-5.
2010: Pen-Hua Su; Jia-Yuh Chen; Chin-Lung Chiang; Yan-Yan Ng; Suh-Jen Chen
Exclusion of MYF5, GSC, RUNX2, and TCOF1 mutation in a case of cerebro-costo-mandibular syndrome.
Clinical dysmorphology 2010;19(2):51-5.
2010: Chi-Yung So; Yan-Yan Ng; Chih-Yu Peng; Jui-Ming Hu; Suh-Jen Chen; Jia-Yuh Chen; Pen-Hua Su
Successful weaning of a laryngeal mask airway after a tongue-lip adhesion operation in a case with cerebro-costo-mandibular syndrome.
Pediatrics and neonatology 2010;51(1):57-60.
2009: Pen-Hua Su; Jia-Yuh Chen; Inn-Chi Lee; Yan-Yan Ng; Jui-Ming Hu; Suh-Jen Chen
Pfeiffer-like syndrome with holoprosencephaly: a newborn with maternal smoking and alcohol exposure.
Pediatrics and neonatology 2009;50(5):234-8.
2008: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Teng-Fu Tsao; Yu-Jie Lai
Sacral dysgenesis associated with terminal deletion of chromosome 7 (q36-qter).
Pediatrics and neonatology 2008;49(5):189-92.
2008: Pen-Hua Su; Shu-Li Wang; Jia-Yuh Chen; Jui-Ming Hu; Hua-Pin Chang; Suh-Jen Chen
Transthyretin levels are not related to Apgar score in low birth weight and very low birth weight infants.
Early human development 2008;84(8):533-8.
2008: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Kai-Chi Yang
Terminal deletion of chromosome 6q.
Pediatrics and neonatology 2008;49(3):88-93.
2008: Yi-Jen Hou; Fong-Lin Chen; Yan-Yan Ng; Jui-Ming Hu; Suh-Jen Chen; Jia-Yuh Chen; Pen-Hua Su
Trisomy 18 syndrome with incomplete Cantrell syndrome.
Pediatrics and neonatology 2008;49(3):84-7.
2008: Yeak-Wun Quek; Pen-Hua Su; Teng-Fu Tsao; Jia-Yuh Chen; Yan-Yan Ng; Jui-Ming Hu; Suh-Jen Chen
Hydranencephaly associated with interruption of bilateral internal carotid arteries.
Pediatrics and neonatology 2008;49(2):43-7.
2008: Pen-Hua Su; Shu-Li Wang; Jia-Yuh Chen; Suh-Jen Chen; Jui-Chen Ke
A study of anthropomorphic and biochemical characteristics in girls with central precocious puberty and thelarche variant.
Journal of pediatric endocrinology & metabolism : JPEM 2008;21(3):213-20.
2007: Pen-Hua Su; Ju-Shan Yu; Jia-Yuh Chen; Suh-Jen Chen; Shuan-Yow Li; Hsiao-Neng Chen
Mutations and new polymorphic changes in the TCOF1 gene of patients with oculo-auriculo-vertebral spectrum and Treacher-Collins syndrome.
Clinical dysmorphology 2007;16(4):261-7.
2007: Pen-Hua Su; Jia-Yuh Chen; Chih-Hao Hsu; Suh-Jen Chen; Si-Wa Chan; Li-Ling Lin
Trisomy 18 with multiple rare malformations: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2007;48(5):272-5.
2007: Pen-Hua Su; Pao-Lin Kuo; Suh-Jen Chen; Jia-Yuh Chen; Ju-Shan Yu; Yuh-Ling Liu; I-Wen Kao
Kabuki make-up (Niikawa-Kuroki) syndrome with mosaicism ring chromosome X and incomplete XIST gene expression.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2007;48(1):28-31.
2007: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Ming-Shiang Yang; I-Wen Kao; Chin-Yi Tsai
Deletion of chromosome region 18q21.3-->qter in a patient: clinical, endocrine and imaging abnormalities.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2007;48(1):23-7.
2006: Chih-Fang Lee; Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Kai-Chi Yang; Li-Ling Lin
Short stature in patients with 45,X/46,XY mosaicism: report of three cases.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2006;47(6):312-6.
2006: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Li-Ling Lin
Clinical manifestations of chromosome 21 interstitial deletion: report of four cases.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2006;47(6):303-8.
2006: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Ming-Shiang Yang; Yuh-Ling Liu
Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q.
Clinical dysmorphology 2006;15(4):225-8.
2006: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Huei-Mei Hung; Hung-Chih Ting; Ching-Yi Lin; Yeak Wen Quek
45,X/46,XX mosaicism in a mother and one of her discordant monozygotic twin daughters: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2006;47(5):252-4.
2006: Pen-Hua Su; Jia-Yu Chen; Suh-Jen Chen; Ju-Shan Yu
Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.
Journal of the Formosan Medical Association = Taiwan yi zhi 2006;105(6):518-21.
2006: Yan-Yan Ng; Jui-Ming Hu; Pen-Hua Su; Jia-Yuh Chen; Ming-Shiang Yang; Suh-Jen Chen
Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2006;47(3):142-5.
2005: Pen-Hua Su; Shu-Li Wang; Chin-Yu Lin; Jia-Yuh Chen; Cheng-Pin Changlai; Shu-Hua Jian; Suh-Jen Chen
Leptin changes in Taiwanese girls with central precocious puberty before and during the GnRH agonist treatment.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2005;46(5):278-83.
2005: Pen-Hua Su; Shi-Ping Luh; Da-Mien Yieh; Jia-Yuh Chen; Suh-Jen Chen; Huei-Mei Hung; Pei-Fen Liao
Anterior mediastinal immature teratoma with precocious puberty in a child with Klinefelter syndrome.
Journal of the Formosan Medical Association = Taiwan yi zhi 2005;104(8):601-4.
2005: Pen-Hua Su; Pao-Lin Kuo; Suh-Jen Chen; Shu-Chi Huang; Jia-Yuh Chen; Huei-Mei Hung
Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation.
Journal of the Formosan Medical Association = Taiwan yi zhi 2005;104(7):525-30.
2004: Pen-Hua Su; Jia-Yuh Chen; Suh-Jen Chen; Huei-Mei Hung
Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation.
Journal of the Formosan Medical Association = Taiwan yi zhi 2004;103(11):853-7.
2004: Pen-Hua Su; Jia-Yuh Chen; Ju-Shan Yu; Chi-Ming Su; Tzu-Ching Huang; Suh-Jen Chen
De Novo incontinentia pigmenti in female twins.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2004;45(3):178-80.
2004: Pen-Hua Su; Suh-Jen Chen; Inn-Chi Lee; Kao-Lun Wang; Jia-Yuh Chen; Huei-Mei Hung; Chih-Fang Lee
Interstitial deletion of chromosome 14q in a Taiwanese infant with microcephaly.
Journal of the Formosan Medical Association = Taiwan yi zhi 2004;103(5):385-7.
2002: Pen-Hua Su; Jia-Yuh Chen; Huei-Mei Hung; Jung-Pin Chen; Ching-Ming Wang; Suh-Jen Chen
Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation.
Journal of the Formosan Medical Association = Taiwan yi zhi 2002;101(4):301-3.