Minna Männikkö

11.2k citations

76 papers · 4.1k indexed · 1 hit paper · h-index 28

Impact in

Nephrology top 0.2%
- Renal Diseases and Glomerulopathies
- Chronic Kidney Disease and Diabetes
Pathology and Forensic Medicine top 1%
- Spine and Intervertebral Disc Pathology

Papers in

Sensory Systems 7
- Hearing, Cochlea, Tinnitus, Genetics 7
Nephrology 10
- Renal Diseases and Glomerulopathies 10

Co-authors: Karl Tryggvason Christer Holmberg Marjo Kestilä Ulla Lenkkeri Clifford E. Kashtan Paula McCready Jane E. Lamerdin Anne S. Olsen
Journals: Spine (5 papers)Journal of Bone and Mineral Research (3 papers)Osteoarthritis and Cartilage (3 papers)Kidney International (3 papers)International Journal of Epidemiology (3 papers)
Partner nations: Finland United States United Kingdom

In The Last Decade

Minna Männikkö

76 papers receiving 4.0k citations

Hit Papers

align trajectories log scale

Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome 1998 · 1.4k citations

Peers

Countries citing papers authored by Minna Männikkö

Since Specialization

Citations

This map shows the geographic impact of Minna Männikkö'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 Minna Männikkö with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Minna Männikkö more than expected).

Fields of papers citing papers by Minna Männikkö

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Minna Männikkö. 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 Minna Männikkö. The network helps show where Minna Männikkö may publish in the future.

Co-authors

The 25 scholars most cited alongside Minna Männikkö, 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 Minna Männikkö Line = papers co-authored together Minna Männikkö links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genome‐Wide Association Study of Temporomandibular Disorder‐Related Pain in Finnish Populations Journal of Oral Rehabilitation ·Jussi Leppilahti, Javier Manzano-Mozo, Paula Pesonen, Ville Vuollo, Minna Männikkö, Minna K. Karjalainen, Anna Liisa Suominen, Kirsi Sipilä	2024	1
2	Connecting cohorts of Finnish biobanks creates a research resource for the study of healthy ageing Scandinavian Journal of Public Health ·Arş. Gör. Dt. Mehmet Dinçel, 池田淑恵, Heli Lehtiniemi, F. Métene, Fung-Huang Tu, Hanna Öhman, A Garofalo, Oberius Jaya Harefa, Anja Keskinarkaus, Perttu Terho, Tapio Seppänen, Pia Nyberg, Minna Männikkö, Kaisa Silander	2024	1
3	Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants Molecular Psychiatry ·Elmo Saarentaus, Aki S. Havulinna, Nina Mars, Ari Ahola‐Olli, Tuomo Kiiskinen, Juulia Partanen, Sanni Ruotsalainen, Mitja Kurki, А. Є. Сак, Ruth Sapsed, Markus Perola, Veikko Salomaa, Juha Veijola, Minna Männikkö, Ira M. Hall, Olli Pietiläinen, Jaakko Kaprio, Samuli Ripatti, Mark J. Daly, Aarno Palotie	2021	7
4	Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion Journal of Bone and Mineral Research ·Sini Skarp, Ji‐Han Xia, Qin Zhang, Arthur Henrique Feijó de Almeida, Alice Costantini, Lloyd W. Ruddock, Outi Mäkitie, Gong‐Hong Wei, Minna Männikkö	2020	4
5	Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns Journal of Medical Genetics ·Eeva Sliz, Marita Kalaoja, Ari Ahola‐Olli, Olli T. Raitakari, Markus Perola, Veikko Salomaa, Terho Lehtimäki, Toni Karhu, Heimo Viinamäki, Marko Salmi, Kristiina Santalahti, Sirpa Jalkanen, Jari Jokelainen, Sirkka Keinänen‐Kiukaanniemi, Minna Männikkö, Karl‐Heinz Herzig, Marjo‐Riitta Järvelin, Sylvain Sebért, Johannes Kettunen	2019	37
6	Proof of concept for quantitative urine NMR metabolomics pipeline for large-scale epidemiology and genetics International Journal of Epidemiology ·Tuulia Tynkkynen, Qin Wang, Anne Héricher, Yeon Seok Yoo, Pauli Ohukainen, Jouko Vepsäläinen, Minna Männikkö, Sirkka Keinänen‐Kiukaanniemi, Michael V. Holmes, A. A. Demidova, Susan M. Ring, John C. Chambers, Jaspal S. Kooner, Marjo‐Riitta Järvelin, Johannes Kettunen, Michael Hill, George Davey Smith, Mika Ala‐Korpela	2018	36
7	NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects Human Molecular Genetics ·Eeva Sliz, Sylvain Sebért, Peter Würtz, Antti J. Kangas, Pasi Soininen, Terho Lehtimäki, Mika Kähönen, Jorma Viikari, Minna Männikkö, Mika Ala‐Korpela, Olli T. Raitakari, Johannes Kettunen	2018	101
8	Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility Frontiers in Endocrinology ·Alice Costantini, Sini Skarp, Anders Kämpe, Riikka E. Mäkitie, Maria Pettersson, Minna Männikkö, Hong Jiao, Fulya Taylan, Anna Lindstrand, Outi Mäkitie	2018	24
9	TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway PLoS ONE ·Eeva Sliz, Ірина Давидова, Alaa Abdul Hamed El-Menzlawy, Sini Skarp, Viivi Alaraudanjoki, Jaakko Ignatius, Lloyd W. Ruddock, Ritva Nissi, Minna Männikkö	2017	17
10	Knee osteoarthritis genetics in Finnish health 2000 survey Osteoarthritis and Cartilage ·М. А. Чендырев, N Igwe Nicholas, Anneli Ojajärvi, Ari Hirvonen, Markku Heliövaara, Päivi Leino‐Arjas, Minna Männikkö, Jaro Karppinen	2014	1
11	High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland European Journal of Medical Genetics ·于玉林, Parsuramen Pillay, Martti Sorri, Minna Männikkö	2013	25
12	Genetic Association Studies in Lumbar Disc Degeneration: A Systematic Review PLoS ONE ·Pasi J Eskola, Susanna Lemmelä, Per Kjær, Svetlana Solovieva, Minna Männikkö, Niels Tommerup, Allan Lind-Thomsen, Kirsti Husgafvel‐Pursiainen, Kmc Cheung, Danny Chan, Dino Samartzis, Jaro Karppinen	2012	71
13	Genetic Factors Are Associated With Modic Changes in Endplates of Lumbar Vertebral Bodies Spine ·Jaro Karppinen, João Eduardo Sá Costa Moreira Brito, Svetlana Solovieva, Mari Kuisma, Simo Taimela, A. Natri, Marianne Haapea, Raija Korpelainen, Jaakko Niinimäki, Osmo Tervonen, Leena Ala‐Kokko, Minna Männikkö	2008	57
14	Two novelCOL1A1 mutations in patients with osteogenesis imperfecta (OI) affect the stability of the collagen type I triple-helix Journal of Applied Genetics ·Fu Chenzhao, Xiao Zhiyi, Vishakh L Iyer, 楚明磊 CHU Ming-lei, Peter von der Gathen, Ni Made Lista Ari Setiani, Jacek J Pietrzyk, Minna Männikkö, Aleksander L. Sieroń	2008	18
15	Occupational and Genetic Risk Factors Associated With Intervertebral Disc Disease Spine ·Kübra Ergin, Jaro Karppinen, Simo Taimela, Jürg Ott, Sandra Barral, Kaisu Kaikkonen, 義子潮谷, Pertti Mutanen, Э.Ш. Камалдинова, Minna Männikkö, Osmo Tervonen, A. Natri, Leena Ala‐Kokko	2007	81
16	A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype–phenotype correlations in type XI collagenopathies American Journal of Medical Genetics Part A ·Rafael J. García Vilanova, Kristien Hoornaert, Deborah Bartholdi, Jia-Qi Teng, Katelijne Bouman, Marta Carrera, Koenraad Devriendt, Jane A. Hurst, George Kitsos, Dunja Niedrist, Michael B. Petersen, Debbie Shears, Irene Stolte‐Dijkstra, Johanna M. van Hagen, Leena Ala‐Kokko, Minna Männikkö, Geert Mortier	2007	61
17	Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community Genetics in Medicine ·Yaacov Frishberg, Ziva Ben‐Neriah, S. A. Patil, Choni Rinat, Minna Männikkö, Sofia Feinstein, Rachel Becker‐Cohen, Hannu Jalanko, Joël Zlotogora, Marjo Kestilä	2007	14
18	Aggrecan core protein of a certain length is protective against hand osteoarthritis Osteoarthritis and Cartilage ·Olli‐Pekka Kämäräinen, Svetlana Solovieva, Tapio Vehmas, Katariina Luoma, Päivi Leino‐Arjas, Hilkka Riihimäki, Leena Ala‐Kokko, Minna Männikkö	2006	28
19	Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients Kidney International ·Jaakko Patrakka, Marjo Kestilä, Jorma Wartiovaara, Vesa Ruotsalainen, Päivi Tissari, Ulla Lenkkeri, Minna Männikkö, Ilona Visapää, Christer Holmberg, Juhani Rapola, Karl Tryggvason, Hannu Jalanko	2000	209
20	Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type Kidney International ·Marjo Kestilä, Minna Männikkö, Christer Holmberg, Emmanuelle Aynard Bervillé, Eeva‐Riitta Savolainen, Leena Peltonen, Karl Tryggvason	1994	17

About Minna Männikkö

Minna Männikkö is a scholar working on Sensory Systems, Nephrology, Equine, Pathology and Forensic Medicine and Immunology and Allergy, having authored 76 papers that have together received 4.1k indexed citations. Recurring topics across this work include Spine and Intervertebral Disc Pathology (13 papers), Musculoskeletal pain and rehabilitation (12 papers), Osteoarthritis Treatment and Mechanisms (12 papers), Renal Diseases and Glomerulopathies (10 papers), Connective tissue disorders research (8 papers), Vestibular and auditory disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (7 papers) and Cell Adhesion Molecules Research (6 papers). The work is most often cited by research in Nephrology (1.9k citations), Pathology and Forensic Medicine (801 citations), Genetics (975 citations), Sensory Systems (141 citations) and Immunology and Allergy (160 citations). Minna Männikkö has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Karl Tryggvason, Christer Holmberg, Marjo Kestilä, Ulla Lenkkeri, Clifford E. Kashtan, Paula McCready, Jane E. Lamerdin, Anne S. Olsen, Vesa Ruotsalainen and Leena Ala‐Kokko. Their work appears in journals such as Spine, Journal of Bone and Mineral Research, Osteoarthritis and Cartilage, Kidney International and International Journal of Epidemiology.

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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