Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan; Korean Consortium of Hereditary Renal Diseases in Children; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group); NEPHROVIR

doi:10.1016/j.kint.2020.05.029

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan
, Korean Consortium of Hereditary Renal Diseases in Children
, Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group)
, NEPHROVIR

Pediatrics

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1308-1322
Number of pages	15
Journal	Kidney International
Volume	98
Issue number	5
DOIs	https://doi.org/10.1016/j.kint.2020.05.029
State	Published - Nov 2020

ASJC Scopus Subject Areas

Nephrology

Keywords

glomerulus
nephrotic syndrome
pediatric nephrology
podocyte

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10.1016/j.kint.2020.05.029

Cite this

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan, Korean Consortium of Hereditary Renal Diseases in Children, Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group), & NEPHROVIR (2020). Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. Kidney International, 98(5), 1308-1322. https://doi.org/10.1016/j.kint.2020.05.029

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. / The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan; Korean Consortium of Hereditary Renal Diseases in Children; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group) et al.
In: Kidney International, Vol. 98, No. 5, 11.2020, p. 1308-1322.

Research output: Contribution to journal › Article › peer-review

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan, Korean Consortium of Hereditary Renal Diseases in Children, Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group) & NEPHROVIR 2020, 'Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome', Kidney International, vol. 98, no. 5, pp. 1308-1322. https://doi.org/10.1016/j.kint.2020.05.029

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan, Korean Consortium of Hereditary Renal Diseases in Children, Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group), NEPHROVIR. Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. Kidney International. 2020 Nov;98(5):1308-1322. doi: 10.1016/j.kint.2020.05.029

The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan ; Korean Consortium of Hereditary Renal Diseases in Children ; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group) et al. / Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. In: Kidney International. 2020 ; Vol. 98, No. 5. pp. 1308-1322.

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title = "Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome",

keywords = "glomerulus, nephrotic syndrome, pediatric nephrology, podocyte",

author = "\{The Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan\} and \{Korean Consortium of Hereditary Renal Diseases in Children\} and \{Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group)\} and NEPHROVIR and Xiaoyuan Jia and Tomohiko Yamamura and Rasheed Gbadegesin and McNulty, \{Michelle T.\} and Kyuyong Song and China Nagano and Yuki Hitomi and Dongwon Lee and Yoshihiro Aiba and Khor, \{Seik Soon\} and Kazuko Ueno and Yosuke Kawai and Masao Nagasaki and Eisei Noiri and Tomoko Horinouchi and Hiroshi Kaito and Riku Hamada and Takayuki Okamoto and Koichi Kamei and Yoshitsugu Kaku and Rika Fujimaru and Ryojiro Tanaka and Yuko Shima and Yoshinori Araki and Yoshinobu Nagaoka and Yasuyuki Sato and Asako Hayashi and Toshiyuki Takahashi and Hayato Aoyagi and Michihiko Ueno and Masanori Nakanishi and Nariaki Toita and Kimiaki Uetake and Norio Kobayashi and Shoji Fujita and Kazushi Tsuruga and Naonori Kumagai and Hiroki Kudo and Eriko Tanaka and Tae Omori and Mari Okada and Yoshiho Hatai and Tomohiro Udagawa and Yaeko Motoyoshi and Kenji Ishikura and Masao Ogura and Mai Sato and Yuji Kano and Motoshi Hattori and Abiodun Omoloja",

note = "Publisher Copyright: {\textcopyright} 2020 International Society of Nephrology",

year = "2020",

month = nov,

doi = "10.1016/j.kint.2020.05.029",

language = "English",

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AU - Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group)

AU - NEPHROVIR

AU - Jia, Xiaoyuan

AU - Yamamura, Tomohiko

AU - Gbadegesin, Rasheed

AU - McNulty, Michelle T.

AU - Song, Kyuyong

AU - Nagano, China

AU - Hitomi, Yuki

AU - Lee, Dongwon

AU - Aiba, Yoshihiro

AU - Khor, Seik Soon

AU - Ueno, Kazuko

AU - Kawai, Yosuke

AU - Nagasaki, Masao

AU - Noiri, Eisei

AU - Horinouchi, Tomoko

AU - Kaito, Hiroshi

AU - Hamada, Riku

AU - Okamoto, Takayuki

AU - Kamei, Koichi

AU - Kaku, Yoshitsugu

AU - Fujimaru, Rika

AU - Tanaka, Ryojiro

AU - Shima, Yuko

AU - Araki, Yoshinori

AU - Nagaoka, Yoshinobu

AU - Sato, Yasuyuki

AU - Hayashi, Asako

AU - Takahashi, Toshiyuki

AU - Aoyagi, Hayato

AU - Ueno, Michihiko

AU - Nakanishi, Masanori

AU - Toita, Nariaki

AU - Uetake, Kimiaki

AU - Kobayashi, Norio

AU - Fujita, Shoji

AU - Tsuruga, Kazushi

AU - Kumagai, Naonori

AU - Kudo, Hiroki

AU - Tanaka, Eriko

AU - Omori, Tae

AU - Okada, Mari

AU - Hatai, Yoshiho

AU - Udagawa, Tomohiro

AU - Motoyoshi, Yaeko

AU - Ishikura, Kenji

AU - Ogura, Masao

AU - Sato, Mai

AU - Kano, Yuji

AU - Hattori, Motoshi

AU - Omoloja, Abiodun

PY - 2020/11

Y1 - 2020/11

KW - glomerulus

KW - nephrotic syndrome

KW - pediatric nephrology

KW - podocyte

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JO - Kidney International

JF - Kidney International

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ER -

Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome

ASJC Scopus Subject Areas

Keywords

Access to Document

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