Go Hun Seo

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 11

Top Topics

Low Density Lipoprotein

Bioinformatics Analysis

Top Venues

Molecular genetics & genomic medicine

Journal of Korean medical science

This page only lists publications with an associated author ORCID identifier.

Publications

Yongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, Go Hun Seo, Hane Lee
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLR. Molecular genetics & genomic medicine 12 (3) (2024)
Jun Hee Cho, Soojin Hwang, Yoon Hae Kwak, Mi-Sun Yum, Go Hun Seo, June-Young Koh, Young Seok Ju, Ji-Hee Yoon, Minji Kang, Hyo-Sang Do, Soyoung Kim, Gu-Hwan Kim, Hyunwoo Bae, Beom-Hee Lee
Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature. Molecular genetics & genomic medicine 12 (4) (2024)
Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Lee
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine 12 (3) (2024)
Yongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, Go Hun Seo, Hane Lee
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLR. Molecular genetics & genomic medicine 12 (3) (2024)
Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Lee
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine (2024)
Jun Hee Cho, Soojin Hwang, Yoon Hae Kwak, Mi-Sun Yum, Go Hun Seo, June-Young Koh, Young Seok Ju, Ji-Hee Yoon, Minji Kang, Hyo-Sang Do, Soyoung Kim, Gu-Hwan Kim, Hyunwoo Bae, Beom-Hee Lee
Clinical and genetic characteristics of three patients with congenital insensitivity to pain with anhidrosis: Case reports and a review of the literature. Molecular genetics & genomic medicine 12 (4) (2024)
Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Lee
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine 12 (3) (2024)
Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Lee
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine 12 (3) (2024)
Yongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, Go Hun Seo, Hane Lee
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLR. Molecular genetics & genomic medicine 12 (3) (2024)
Seung Woo Ryu, Ji-Hee Yoon, Dong-Wook Kim, Beomman Han, Heonjong Han, Joohyun Han, Hane Lee, Go Hun Seo, Beom Hee Lee
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular genetics & genomic medicine 12 (3) (2024)
Jisun Park, Dong Jun Ha, Go Hun Seo, Seri Maeng, Sung Mo Kang, Su Jin Kim, Ji Eun Lee
Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka Syndrome. Journal of Korean medical science 36 (18) (2021)