FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Hyung-Goo Kim

Research Profile

Disorders

Physiology

Chemicals & Drugs

Anatomy

Procedures

Living Beings

Mouse

Genes & Molecular Sequences

Devices

Microarray Analysis

Co-author Network

Publications

TOP 3
Lam S Nguyen; Jill A Rosenfeld; Lisa G Shaffer; Yiping Shen; James F Gusella; Hyung-Goo Kim; Yves Lacassie; Lawrence C Layman; Jozef Gecz
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.
Eric T Siegel; Hiromi Koso Nishimoto; Hyung-Goo Kim; Lawrence C Layman
The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models.
Samuel D Quaynor; Richard J Sherins; Tiera Williams; David P Bick; Elizabeth M Cappello; Lynn P Chorich; Hyung-Goo Kim; Lawrence C Layman
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Hyung-Goo Kim (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Lam S Nguyen; Jill A Rosenfeld; Lisa G Shaffer; Yiping Shen; James F Gusella; Hyung-Goo Kim; Yves Lacassie; Lawrence C Layman; Jozef Gecz
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.
Human molecular genetics 2013;22(9):1816-25.
2013: Eric T Siegel; Hiromi Koso Nishimoto; Hyung-Goo Kim; Lawrence C Layman
The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models.
Reproductive sciences (Thousand Oaks, Calif.) 2013;20(3):211-33.
2011: Samuel D Quaynor; Richard J Sherins; Tiera Williams; David P Bick; Elizabeth M Cappello; Lynn P Chorich; Hyung-Goo Kim; Lawrence C Layman
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Fertility and sterility 2011;96(6):1424-1430.e6.
2011: Hyung-Goo Kim; Lawrence C Layman
The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Molecular and cellular endocrinology 2011;346(1-2):74-83.
2011: Ning Xu; Hyung-Goo Kim; Balasubramanian Bhagavath; Sung-Gyu Cho; Jae Ho Lee; Kyungsoo Ha; Irene Meliciani; Wolfgang Wenzel; Robert Podolsky; Lynn P Chorich; Kathryn A Stackhouse; Anna M H Grove; Lawrence N Odom; metin ozata; David P Bick; Richard J Sherins; Soo-Hyun Kim; Richard S Cameron; Lawrence C Layman
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Fertility and sterility 2011;95(5):1613-20.e1-7.
2011: Shobhit Jain; Hyung-Goo Kim; Ingo Kurth; Felicitas Lacbawan; Lawrence C Layman; Irene Meliciani; Morris Schoeneman; Josefina Sharma; Svetlana Ten; Wolfgang Wenzel; Elka Jacobson-Dickman
Unique phenotype in a patient with CHARGE syndrome.
International journal of pediatric endocrinology 2011;2011():11.
2010: Hyung-Goo Kim; Jang-Won Ahn; Ingo Kurth; Reinhard Ullmann; Hyun-Taek Kim; Anita S Kulharya; Kyung-Soo Ha; Yasuhide Itokawa; Irene Meliciani; Wolfgang Wenzel; Deresa Lee; Georg Rosenberger; metin ozata; David P Bick; Richard J Sherins; Takahiro Nagase; Mustafa Tekin; Soo-Hyun Kim; Cheol-Hee Kim; Hans-Hilger Ropers; James Gusella; Vera Kalscheuer; Cheol Yong Choi; Lawrence C Layman
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
American journal of human genetics 2010;87(4):465-79.
2010: Ning Xu; Balasubramanian Bhagavath; Hyung-Goo Kim; Lisa Halvorson; Robert Podolsky; Lynn P Chorich; Puttur D Prasad; Wencheng Xiong; Richard S Cameron; Lawrence C Layman
NELF is a nuclear protein involved in hypothalamic GnRH neuronal migration.
Molecular and cellular endocrinology 2010;319(1-2):47-55.
2010: Majid Aminzadeh; Hyung-Goo Kim; Lawrence C Layman; Timothy D Cheetham
Rarer syndromes characterized by hypogonadotropic hypogonadism.
Frontiers of hormone research 2010;39():154-67.
2010: Hyung-Goo Kim; Jennifer Pedersen-White; Balasubramanian Bhagavath; Lawrence C Layman
Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutations.
Frontiers of hormone research 2010;39():94-110.
2008: Hyung-Goo Kim; Ingo Kurth; Fei Lan; Irene Meliciani; Wolfgang Wenzel; Soo Hyun Eom; Gil Bu Kang; Georg Rosenberger; Mustafa Tekin; metin ozata; David P Bick; Richard J Sherins; Steven L Walker; Yang Shi; James Gusella; Lawrence C Layman
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
American journal of human genetics 2008;83(4):511-9.
2008: Hyung-Goo Kim; Balasubramanian Bhagavath; Lawrence C Layman
Clinical manifestations of impaired GnRH neuron development and function.
Neuro-Signals 2008;16(2-3):165-82.
2008: Hyung-Goo Kim; Shotaro Kishikawa; Anne W Higgins; Ihn Sik Seong; Diana J Donovan; Yiping Shen; Eric Lally; Lauren A Weiss; Juliane Najm; Kerstin Kutsche; Maria Descartes; Lynn Holt; Stephen Braddock; Robin Troxell; Lee Kaplan; Fred Volkmar; Ami Klin; Katherine Tsatsanis; David J Harris; Ilse Noens; David L Pauls; Mark J Daly; Marcy E MacDonald; Cynthia C Morton; Bradley J Quade; James Gusella
Disruption of neurexin 1 associated with autism spectrum disorder.
American journal of human genetics 2008;82(1):199-207.
2007: Benjamin Abo-Dalo; Hyung-Goo Kim; Melanie Roes; Margarita Stefanova; Anne Higgins; Yiping Shen; Stefan Mundlos; Bradley J Quade; James Gusella; Kerstin Kutsche
Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
American journal of medical genetics. Part A 2007;143A(22):2668-74.
2007: Weining Lu; Albertien M van Eerde; Xueping Fan; Fabiola Quintero-Rivera; Shashikant Kulkarni; Heather Ferguson; Hyung-Goo Kim; Yanli Fan; Qiongchao Xi; Qing-Gang Li; Damien Sanlaville; William Andrews; Vasi Sundaresan; Weimin Bi; Jiong Yan; Jacques C Giltay; Cisca Wijmenga; Tom de Jong; Sally A Feather; Adrian S Woolf; Yi Rao; James R Lupski; Michael Eccles; Bradley J Quade; James Gusella; Cynthia C Morton; Richard L Maas
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.
American journal of human genetics 2007;80(4):616-32.
2007: Hyung-Goo Kim; Anne W Higgins; Steven R Herrick; Shotaro Kishikawa; Linda Nicholson; Kerstin Kutsche; Azra H Ligon; David J Harris; Marcy E MacDonald; Gail A P Bruns; Cynthia C Morton; Bradley J Quade; James Gusella
Candidate loci for Zimmermann-Laband syndrome at 3p14.3.
American journal of medical genetics. Part A 2007;143(2):107-11.
2006: Hye-Jin Jeong; Hyun Jae Kim; Sook-Hwan Lee; KyuBum Kwack; So-Yeon Ahn; Yoon-Jeong Choi; Hyung-Goo Kim; Kyo-Won Lee; Chung-No Lee; Kwang-Yul Cha
Gene expression profiling of the pre-implantation mouse embryo by microarray analysis: comparison of the two-cell stage and two-cell block.
Theriogenology 2006;66(4):785-96.