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J

Juha Kere

karolinska institutetProfessor/Senior Physician, Molecular Genetics, Department of Medicine, Huddinge
H指数:112
被引数:4.9万

个人简介

Juha Kere (born 1958) is professor of molecular genetics at KI since 2001. He graduated with MD (1984), PhD in molecular genetics (1989) and specialist physician degree in clinical genetics (1994) from University of Helsinki. He was postdoctoral associate at Washington University in St.Louis, Missouri 1990-93 and became acting professor and chief physician of medical genetics at University of Helsinki and Helsinki University Central Hospital 1994. He was then founding director of the Finnish Genome Center 1998-2001, after which he moved to KI. He has published over 640 scientific original and review articles and supervised 54 completed doctoral theses in Finland and Sweden.

教育背景

  • 1984.12

    University of Helsinki MD MD

  • 1989.12

    University of Helsinki PhD PhD in molecular genetics

  • 1994.12

    University of Helsinki specialist physician degree specialist physician degree in clinical genetics

工作经历

  • 2024.01 – 至今

    Karolinska Institutet

    Professor/Senior Physician, Molecular Genetics, Department of Medicine, Huddinge

  • 2001.01 – 2024.12

    Karolinska Institutet

    Professor/Senior Physician, Molecular Genetics, Department of Biosciences and Nutrition

  • 1998.01 – 2001.12

    Finnish Genome Center

    founding director

  • 1994.01 – 至今

    University of Helsinki

    acting professor and chief physician of medical genetics

  • 1994.01 – 至今

    Helsinki University Central Hospital

    acting professor and chief physician of medical genetics

  • 1990.01 – 至今

    Washington University in St.Louis

    postdoctoral associate

荣誉奖项

暂无内容

Integrated Methylome–Transcriptome Analysis Reveals Epigenomic Remodeling and Rho GTPase–Linked Immune–Epithelial Crosstalk in Atopic Dermatitis

整合甲基化组-转录组分析揭示了特应性皮炎中的表观基因组重塑及Rho GTP酶相关的免疫-上皮串扰

Allergy
IF12
2026-02-170
OAAI
Tiina Skoog; Ying Yang; Peter Olah; Shintaro Katayama; Piia Karisola; Catherine Smith; Stephan Weidinger; Jonathan Barker; Antti Lauerma; Björn Andersson; Bernhard Homey; Nanna Fyhrquist; Juha Kere; Harri Alenius; MAARS Consortium
The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

HRAS变异c.175G>A (p.Ala59Thr)导致一种以表皮外胚层为主要表型的表现，缺乏经典科斯蒂奥综合征特征。

American Journal of Medical Genetics Part A
IF1.7
2025-10-010
OAAI
Rautiainen, Nikole; Brandt, Eveliina; Kettunen, Kaisa; Elomaa, Outi; Kivirikko, Sirpa; Jeskanen, Leila; Lappalainen, Katriina; Sjoblom, Nelli; Kere, Juha; Hannula-Jouppi, Katariina; Harjama, Liisa
Novel heterozygous SPI1c.538C>T p.(Leu180Phe) variant causes PU.1 haploinsufficiency leading to agammaglobulinemia

新型杂合SPI1c.538C>T p.(Leu180Phe)变异导致PU.1单倍剂量不足，进而引发无丙种球蛋白血症。

clinical immunology
IF3.8
2025-05-280
PRE
Daddali, Ravindra; Kettunen, Kaisa; Turunen, Tanja; Knox, Ainsley V. C.; Laine, Pia; Chowdhury, Iftekhar; Vanttinen, Markku; Mamia, Nanni; Stiegler, Amy L.; Boggon, Titus J.; Kere, Juha; Romberg, Neil; Seppanen, Mikko R. J.; Varjosalo, Markku; Martelius, Timi; Gronholm, Juha

研究方向

暂未获取到该数据
S
Shintaro Katayama
H 指数:44论文数:171被引数:1.7万
E
Elísabet Einarsdóttir
H 指数:31论文数:140被引数:3,427
C
Cilla Söderhäll
H 指数:43论文数:220被引数:9,990
G
Göran Pershagen
H 指数:115论文数:665被引数:4.5万
E
Erik Melén
H 指数:81论文数:681被引数:2.5万
K
Kaarel Krjutškov
H 指数:33论文数:116被引数:5,922
K
Katariina Hannula‐Jouppi
H 指数:30论文数:87被引数:6,442
T
Tarja Laitinen
H 指数:47论文数:192被引数:1.4万
U
Ulpu Saarialho‐Kere
H 指数:66论文数:231被引数:1.3万
T
Tiina Skoog
H 指数:22论文数:57被引数:1,981