Katariina Kainulainen

3.3k citations

37 papers · 2.5k indexed · h-index 24

Genetics top 2%
Cardiology and Cardiovascular Medicine top 2%
Physiology top 5%
Molecular Biology
Psychiatry and Mental health top 5%

Co-authors: Kimmo Kontula Raimo Sulkava Tuomo Polvikoski Auli Verkkoniemi Leena Peltonen Ilkka Kaitila Lea Puhakka Leena Niinistö
Topics: Connective tissue disorders research (15 papers)Dementia and Cognitive Impairment Research (6 papers)Aortic Disease and Treatment Approaches (4 papers)
Cited by: Genetics Cardiology and Cardiovascular Medicine Psychiatry and Mental health
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Nucleic Acids Research
Partner nations: Finland United States Sweden

In The Last Decade

Katariina Kainulainen

35 papers receiving 2.4k citations

Peers

Countries citing papers authored by Katariina Kainulainen

Since Specialization

Citations

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

Fields of papers citing papers by Katariina Kainulainen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katariina Kainulainen

This figure shows the co-authorship network connecting the top 25 collaborators of Katariina Kainulainen. A scholar is included among the top collaborators of Katariina Kainulainen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Katariina Kainulainen. Katariina Kainulainen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Incidence and outcome of hospital-acquired COVID-19 infections in secondary and tertiary care hospitals in the era of COVID-19 vaccinations 2023 ·SHILAP Revista de lepidopterología ·(unknown),Erik Forsblom,Katariina Kainulainen,Asko Järvinen,Elisa Kortela	0
2	Polymorphism of the angiotensin-converting enzyme (ACE) and angiotesinogen (AGT) genes and their associations with blood pressure and carotid artery intima media thickness among healthy Finnish young adults—the Cardiovascular Risk in Young Finns Study 2006 ·Atherosclerosis ·(unknown),Terho Lehtimäki,Markus Juonala,Mika Kähönen,Nina Hutri‐Kähönen,Katariina Kainulainen,Helena E. Miettinen,Leena Taittonen,Kimmo Kontula,Jorma Viikari,Olli T. Raitakari	19
3	Does Apolipoprotein E Influence Learning and Memory in the Nondemented Oldest Old? 2001 ·International Psychogeriatrics ·(unknown),Raija Ylikoski,Auli Verkkoniemi,Kati Juva,Sari Rastas,Tuomo Polvikoski,Kimmo Kontula,Katariina Kainulainen,Leena Niinistö,Irma‐Leena Notkola,Raimo Sulkava	24
4	Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings 2000 ·Journal of Hypertension ·Markus Perola,Katariina Kainulainen,Päivi Pajukanta,Joseph D. Terwilliger,Tero Hiekkalinna,Pekka Ellonen,Jaakko Kaprio,Markku Koskenvuo,Kimmo Kontula,Leena Peltonen	95
5	Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes 1999 ·Journal of the American College of Cardiology ·Jouko Karjalainen,Urho M. Kujala,(unknown),Matti Mäntysaari,Matti Viitasalo,Katariina Kainulainen,Kimmo Kontula	102
6	Arrhythmic disorder mapped to chromosome 1q42–q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts 1999 ·Journal of the American College of Cardiology ·Heikki Swan,Kirsi Piippo,Matti Viitasalo,(unknown),Timo Paavonen,Katariina Kainulainen,Juha Kere,Pekka Keto,Kimmo Kontula,Lauri Toivonen	238
7	Molecular genetics of the long QT syndrome: Two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred 1998 ·Human Mutation ·(unknown),Heikki Swan,Katariina Kainulainen,Lauri Toivonen,Matti Viitasalo,Kimmo Kontula	42
8	Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes 1998 ·Human Mutation ·Leena Karttunen,(unknown),Katariina Kainulainen,Ann-Christine Syvänen,Leena Peltonen	15
9	Markers for the gene ob and serum leptin levels in human morbid obesity 1997 ·Human Genetics ·Laura Oksanen,Miina K. Öhman,Mark L. Heiman,Katariina Kainulainen,Jaakko Kaprio,Pertti Mustajoki,Veikko A Koivisto,Markku Koskenvuo,Olli A. Jänne,Leena Peltonen,Kimmo Kontula	34
10	Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects 1997 ·International Journal of Obesity ·Laura Oksanen,Katariina Kainulainen,Mark L. Heiman,Pertti Mustajoki,(unknown),Kimmo Kontula	28
11	Common Polymorphism of the Vitamin D Receptor Gene is Associated with Variation of Peak Bone Mass in Young Finns 1996 ·Calcified Tissue International ·Anne Viitanen,M Kärkkäinen,Kalevi Laitinen,Christel Lamberg‐Allardt,Katariina Kainulainen,Leena Räsänen,Jorma Viikari,M Välimäki,Kimmo Kontula	49
12	Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene 1995 ·Human Genetics ·Katariina Kainulainen,Heikki Swan,Helena E. Miettinen,Matti Viitasalo,Liisa Rovamo,Lauri Toivonen,Kimmo Kontula	1
13	Apolipoprotein E, Dementia, and Cortical Deposition of β-Amyloid Protein 1995 ·New England Journal of Medicine ·Tuomo Polvikoski,Raimo Sulkava,Matti Haltia,Katariina Kainulainen,Alpo Vuorio,Auli Verkkoniemi,Leena Niinistö,Pirjo Halonen,Kimmo Kontula	407
14	An extra cysteine in one of the non-calcium-binding epidermal growth factor-like motifs of the FBN1 polypeptide is connected to a novel variant of Marfan syndrome. 1994 ·Journal of Clinical Investigation ·(unknown),(unknown),Katariina Kainulainen,(unknown),(unknown),Kristina Törnqvist,Laura‐Maria Peltonen	27
15	DNA Diagnostics of the MarfanSyndrome: Application ofAmplifîable Polymorphie Markers 1994 ·European Journal of Human Genetics ·Terhi Rantamäki,(unknown),Leena Karttunen,Katariina Kainulainen,Leena Peltonen	9
16	A Novel Mutation of the Fibrillin Gene Causing Ectopia Lentis 1994 ·Genomics ·(unknown),A. H. Child,Katariina Kainulainen,Rebecca M. Davidson,Lea Puhakka,Leena Peltonen	70
17	Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome 1994 ·Nature Genetics ·Katariina Kainulainen,Leena Karttunen,Lea Puhakka,Lynn Y. Sakai,Leena Peltonen	195
18	Elucidation of the gene defect in Marfan syndrome Success by two complementary research strategies 1992 ·FEBS Letters ·(unknown),Katariina Kainulainen	9
19	Location on Chromosome 15 of the Gene Defect Causing Marfan Syndrome 1990 ·New England Journal of Medicine ·Katariina Kainulainen,Leena Pulkkinen,Aslak Savolainen,Ilkka Kaitila,Leena Peltonen	265
20	Progestin induction of 17β‐hydroxysteroid dehydrogenase enzyme protein in the t‐47D human breast‐cancer cell line 1990 ·International Journal of Cancer ·Matti Poutanen,Veli Isomaa,Katariina Kainulainen,R. Vihko	43

About Katariina Kainulainen

Katariina Kainulainen is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Psychiatry and Mental health, having authored 37 papers that have together received 2.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (15 papers), Dementia and Cognitive Impairment Research (6 papers) and Aortic Disease and Treatment Approaches (4 papers). The work is most often cited by research in Genetics (1.0k citations), Cardiology and Cardiovascular Medicine (815 citations) and Psychiatry and Mental health (392 citations). Katariina Kainulainen has collaborated with scholars based in Finland, United States and Sweden. Frequent co-authors include Kimmo Kontula, Raimo Sulkava, Tuomo Polvikoski, Auli Verkkoniemi, Leena Peltonen, Ilkka Kaitila, Lea Puhakka, Leena Niinistö, Matti Haltia and Aslak Savolainen. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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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