Juha Kere

49.7k citations

512 papers · 22.1k indexed · 3 hit papers · h-index 78

Impact in

Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Molecular Biology top 0.2%
- Epigenetics and DNA Methylation
- Ion Transport and Channel Regulation
- dental development and anomalies
- Ion channel regulation and function

Papers in

Genetics 152
- Genetics and Neurodevelopmental Disorders 34
- Genetic Associations and Epidemiology 23
Obstetrics and Gynecology 33
- Pregnancy and preeclampsia studies 29

Co-authors: Ulpu Saarialho‐Kere Albert de la Chapelle Christer Holmberg Shintaro Katayama Annika Scheynius Pia Höglund Lovisa E. Reinius Katariina Hannula‐Jouppi
Journals: PLoS ONE (25 papers)Scientific Reports (21 papers)European Journal of Human Genetics (17 papers)The American Journal of Human Genetics (13 papers)Genomics (13 papers)
Partner nations: Finland Sweden United States

In The Last Decade

Juha Kere

499 papers receiving 21.5k citations

Hit Papers

align trajectories log scale

Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis 2013 · 662 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2013 Nature Biotechnology
2012 PLoS ONE
1996 Nature Genetics

Peers

Countries citing papers authored by Juha Kere

Since Specialization

Citations

This map shows the geographic impact of Juha Kere's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Juha Kere with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Juha Kere more than expected).

Fields of papers citing papers by Juha Kere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Juha Kere. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Juha Kere. The network helps show where Juha Kere may publish in the future.

Co-authors

The 25 scholars most cited alongside Juha Kere, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Juha Kere Line = papers co-authored together Juha Kere links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Polygenic Risk Scores in Predicting Coronary Artery Disease in Symptomatic Patients. A Validation Study Journal of Atherosclerosis and Thrombosis ·I Kujala, Jagadish Vangipurapu, Teemu Maaniitty, Antti Saraste, Juha Kere, Juhani Knuuti	2024	0
2	Viral infection‐related gene upregulation in monocytes in children with signs of β‐cell autoimmunity Pediatric Diabetes ·Milla Valta, Masahito Yoshihara, Elísabet Einarsdóttir, Sirpa Pahkuri, Sini Ezer, Shintaro Katayama, Mikael Knip, Riitta Veijola, Jorma Toppari, Jorma Ilonen, Juha Kere, Johanna Lempainen	2022	1
3	SkewC: Identifying cells with skewed gene body coverage in single-cell RNA sequencing data iScience ·Imad Abugessaisa, Akira Hasegawa, Shuhei Noguchi, Mélissa Cardon, Kazuhide Watanabe, Masataka Takahashi, Harukazu Suzuki, Shintaro Katayama, Juha Kere, Takeya Kasukawa	2022	4
4	Human endometrial cell-type-specific RNA sequencing provides new insights into the embryo–endometrium interplay Human Reproduction Open ·Mariann Koel, Kaarel Krjutškov, Merli Saare, Külli Samuel, Dmitri Lubenets, Shintaro Katayama, Elísabet Einarsdóttir, Eva Vargas, Alberto Sola‐Leyva, Parameswaran Grace Lalitkumar, Kristina Gemzell‐Danielsson, David Blesa, Carlos Simón, Fredrik Lanner, Juha Kere, Andres Salumets, Signe Altmäe	2022	8
5	Differentiation of ciliated human midbrain-derived LUHMES neurons Journal of Cell Science ·Gilbert Lauter, Andrea Coschiera, Masahito Yoshihara, Debora Sugiaman‐Trapman, Sini Ezer, Shalini Sethurathinam, Shintaro Katayama, Juha Kere, Peter Swoboda	2020	9
6	Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation Molecular Neurobiology ·Andrea Bieder, Masahito Yoshihara, Shintaro Katayama, Kaarel Krjutškov, Anna Falk, Juha Kere, Isabel Tapia‐Páez	2020	9
7	Discovering heritable modes of MEG spectral power Human Brain Mapping ·Eemeli Leppäaho, Hanna Renvall, Elina Salmela, Juha Kere, Riitta Salmelin, Samuel Kaski	2019	10
8	Nocturnal asthma is affected by genetic interactions between RORA and NPSR1 Pediatric Pulmonology ·Vincent D. Gaertner, Sven Michel, John A. Curtin, Ville Pulkkinen, Nathalie Acevedo, Cilla Söderhäll, Andrea von Berg, Albrecht Bufe, Otto Laub, Ernst Rietschel, Andrea Heinzmann, Burkhard Simma, Christian Vogelberg, Göran Pershagen, Erik Melén, Angela Simpson, Adnan Ćustović, Juha Kere, Michael Kabesch	2019	5
9	TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting npj Genomic Medicine ·Hindrek Teder, Mariann Koel, Priit Paluoja, Tatjana Jatsenko, Kadri Rekker, Triin Laisk-Podar, Viktorija Kukuškina, Agne Velthut‐Meikas, Olga Fjodorova, Maire Peters, Juha Kere, Andres Salumets, Priit Palta, Kaarel Krjutškov	2018	26
10	The Psoriasis Risk Allele HLA-C06:02 Shows Evidence of Association with Chronic or Recurrent Streptococcal Tonsillitis STM:n Hallinnonalan avoin julkaisuarkisto (Julkari)* ·Karita Haapasalo, Lotta L. E. Koskinen, Jari Suvilehto, Pekka Jousilahti, Annika Wolin, Sari Suomela, Richard C. Trembath, Juliet N. Barker, Jaana Vuopio, Juha Kere, T. Sakari Jokiranta, Päivi Saavalainen	2018	2
11	A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR Scientific Reports ·Satu Wedenoja, Ahlam Khamaysi, Liana Shimshilashvili, Shireen Anbtawe-Jomaa, Outi Elomaa, Jorma Toppari, Pia Höglund, Kristiina Aittomäki, Christer Holmberg, Outi Hovatta, Juha S. Tapanainen, Ehud Ohana, Juha Kere	2017	21
12	Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort Allergy ·Bright I. Nwaru, H.‐M. Takkinen, Onni Niemelä, Minna Kaila, Maijaliisa Erkkola, S. Ahonen, Heidi Tuomi, Anna‐Maija Haapala, Michael G. Kenward, Juha Pekkanen, Riitta Lahesmaa, Juha Kere, Olli Simell, Riitta Veijola, Jorma Ilonen, Heikki Hyöty, Mikael Knip, Suvi Μ. Virtanen	2013	70
13	A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24 Cancer Research ·Huiling He, Rebecca Nagy, Sandya Liyanarachchi, Hong Jiao, Wei Li, Saul Suster, Juha Kere, Albert de la Chapelle	2009	115
14	Biological and genetic interaction between Tenascin C and Neuropeptide S receptor 1 in allergic diseases Human Molecular Genetics ·Christina Orsmark‐Pietras, Erik Melén, Johanna Vendelin, Sara Bruce, Annika Laitinen, Lauri A. Laitinen, Roger Lauener, Josef Riedler, Erika von Mutius, Gert Doekes, Magnus Wickman, Marianne van Hage, Göran Pershagen, Annika Scheynius, Fredrik Nyberg, Juha Kere	2008	24
15	Expression of Allograft Inflammatory Factor-1 in Inflammatory Skin Disorders Acta Dermato Venereologica ·Christina Orsmark, Tiina Skoog, Leila Jeskanen, Juha Kere, Ulpu Saarialho‐Kere	2007	21
16	Hemangioblastomas of the retina: impact of von Hippel-Lindau disease. PubMed ·Mika Niemelä, Sebsebe Lemeta, Markku Sainio, S Rauma, Eero Pukkala, Juha Kere, Tom Böhling, Leila Laatikainen, Juha E. Jääskeläinen, Paula Summanen	2000	35
17	Association Study of the Chromosomal Region Containing the FCER2 Gene Suggests It Has a Regulatory Role in Atopic Disorders American Journal of Respiratory and Critical Care Medicine ·Tarja Laitinen, Vesa Ollikainen, Conxi Lázaro, Paula Kauppi, Rafael de Cid, Josep M. Antó, Xavier Estivill, Heikki Lokki, Heikki Mannila, Lauri A. Laitinen, Juha Kere	2000	33
18	Distinct expression profiles of stromelysin-2 (MMP-10), collagenase-3 (MMP-13), macrophage metalloelastase (MMP-12), and tissue inhibitor of metalloproteinases-3 (TIMP-3) in intestinal ulcerations. PubMed ·Maarit Vaalamo, Marja‐Liisa Karjalainen‐Lindsberg, Pauli Puolakkainen, Juha Kere, Ulpu Saarialho‐Kere	1998	185
19	Human TIMP-3 is expressed during fetal development, hair growth cycle, and cancer progression European Journal of Histochemistry ·Kristiina Airola, Matti Ahonen, Nina Johansson, Pia Heikkilä, Juha Kere, Veli‐Matti Kähäri, Ulpu Saarialho‐Kere	1998	8
20	Paternal isodisomy for chromosome 7 and normal growth and development in a patient with congenital chloride diarrhea The American Journal of Human Genetics ·P. Hoeglund, Albert de la Chapelle, Juha Kere	1994	1

About Juha Kere

Juha Kere is a scholar working on Genetics, Obstetrics and Gynecology, Molecular Biology, Immunology and Immunology and Allergy, having authored 512 papers that have together received 22.1k indexed citations. Recurring topics across this work include Asthma and respiratory diseases (47 papers), Epigenetics and DNA Methylation (43 papers), Genetics and Neurodevelopmental Disorders (34 papers), Pregnancy and preeclampsia studies (29 papers), Ion Transport and Channel Regulation (26 papers), Birth, Development, and Health (24 papers), Genetic Associations and Epidemiology (23 papers) and RNA modifications and cancer (21 papers). The work is most often cited by research in Genetics (5.5k citations), Molecular Biology (10.3k citations), Immunology (3.1k citations), Immunology and Allergy (728 citations) and Cancer Research (1.6k citations). Juha Kere has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Ulpu Saarialho‐Kere, Albert de la Chapelle, Christer Holmberg, Shintaro Katayama, Annika Scheynius, Pia Höglund, Lovisa E. Reinius, Katariina Hannula‐Jouppi, Hannes Lohi and Myriam Peyrard‐Janvid. Their work appears in journals such as PLoS ONE, Scientific Reports, European Journal of Human Genetics, The American Journal of Human Genetics and Genomics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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