K. O. J. Simola

2.0k citations

36 papers · 1.2k indexed · h-index 20

Molecular Biology top 10%
Genetics top 5%
Pediatrics, Perinatology and Child Health top 10%
Clinical Biochemistry top 5%
Genetics top 10%

Co-authors: G.A.P. Bruns Riitta Karikoski Ilkka Kaitila Manfred Gessler Maarit Peippo Anna Pirkola Sakari Knuutila Juha Kere
Topics: Genomic variations and chromosomal abnormalities (12 papers)Prenatal Screening and Diagnostics (9 papers)Chromosomal and Genetic Variations (7 papers)
Cited by: Genetics Clinical Biochemistry Sensory Systems
Journals: Nature Science Proceedings of the National Academy of Sciences
Partner nations: Finland United States Netherlands

In The Last Decade

K. O. J. Simola

36 papers receiving 1.1k citations

Peers

Countries citing papers authored by K. O. J. Simola

Since Specialization

Citations

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

Fields of papers citing papers by K. O. J. Simola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K. O. J. Simola. 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 K. O. J. Simola. The network helps show where K. O. J. Simola may publish in the future.

Co-authorship network of co-authors of K. O. J. Simola

This figure shows the co-authorship network connecting the top 25 collaborators of K. O. J. Simola. A scholar is included among the top collaborators of K. O. J. Simola 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 K. O. J. Simola. K. O. J. Simola 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	Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth 2013 ·Molecular Syndromology ·Nicole Revençu,Laurence M. Boon,A. Dompmartin,Paul N.M.A. Rieu,W Busch,Josée Dubois,Francesca Forzano,Johanna M. van Hagen,Sara Halbach,A. Kuechler,A.M.A. Lachmeijer,Jyrki Lähde,Laura Russell,K. O. J. Simola,John B. Mulliken,Miikka Vikkula	29
2	Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy 2011 ·The American Journal of Human Genetics ·Alexandra Götz,Henna Tyynismaa,Liliya Euro,Pekka Ellonen,Tuulia Hyötyläinen,Tiina Ojala,Riikka H. Hämäläinen,Johanna Tommiska,Taneli Raivio,Matej Orešič,Riitta Karikoski,Outi Tammela,K. O. J. Simola,Anders Paetau,Tiina Tyni,Anu Suomalainen	185
3	Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q 2009 ·Epilepsy Research ·Auli Sirén,Anne Polvi,(unknown),Malgorzata Labuda,(unknown),Anna‐Kaisa Anttonen,Maria Kousi,Kari Hirvonen,K. O. J. Simola,Eva Andermann,Asta Laiho,Juhani T. Soini,(unknown),Reijo Laaksonen,Massimo Pandolfo,Anna‐Elina Lehesjoki	14
4	Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients 2009 ·Journal of Medical Genetics ·R. Douglas Bruce,Katariina Hannula‐Jouppi,(unknown),Ingegerd Fransson,K. O. J. Simola,Marita Lipsanen‐Nyman,Juha Kere	52
5	Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome 2009 ·Journal of Medical Genetics ·Horacio Astudillo‐de la Vega,Alison Trainer,Miriam Gordillo,Moira Crosier,Hülya Kayserili,Flemming Skovby,Maria Luisa Giovannucci Uzielli,Rhonda E. Schnur,Sylvie Manouvrier,E Blair,Jane A. Hurst,Francesca Forzano,Moritz Meins,K. O. J. Simola,Annick Raas‐Rothschild,Raoul C. M. Hennekam,Ethylin Wang Jabs	61
6	Pitt–Hopkins syndrome in two patients and further definition of the phenotype 2006 ·Clinical Dysmorphology ·Maarit Peippo,K. O. J. Simola,Leena Valanne,(unknown),Marketta Kähkönen,Mari Auranen,Jaakko Ignatius	43
7	SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype 2005 ·Human Mutation ·Elke Botzenhart,Andrew Green,Helena G. Ilyina,Rainer König,R. Brian Lowry,Ivan F. M. Lo,Mordechai Shohat,Leah W. Burke,Julie McGaughran,(unknown),Geneviève Pierquin,Ron C. Michaelis,Margo L. Whiteford,K. O. J. Simola,Bernd Rösler,Jürgen Kohlhase	48
8	Cancer incidence in families with multiple glioma patients 2001 ·International Journal of Cancer ·(unknown),Eero Pukkala,Pékka Laippala,Risto Sankila,Jorma Isola,Helena E. Miettinen,K. O. J. Simola,Pauli Helén,Heikki Helin,Hannu Haapasalo	26
9	Analysis of p53 Tumor Suppressor Gene in Families with Multiple Glioma Patients 2001 ·Journal of Neuro-Oncology ·(unknown),Kirsi Syrjäkoski,Risto Sankila,K. O. J. Simola,Pauli Helén,Mika Niemelä,Mika Matikainen,J Isola,Hannu Haapasalo	23
10	Chromosome imbalances in familial gliomas detected by comparative genomic hybridization 2000 ·Genes Chromosomes and Cancer ·(unknown),Satu‐Leena Sallinen,Ritva Karhu,Helena E. Miettinen,P Sallinen,Juha Kononen,Pékka Laippala,K. O. J. Simola,(unknown),Hannu Haapasalo	22
11	Applicability of a checklist for clinical screening of the fragile X syndrome 1997 ·Clinical Genetics ·Maria Arvio,Maarit Peippo,K. O. J. Simola	31
12	Usher's syndrome type 3 in Finland 1995 ·The Laryngoscope ·Leenamaija Pakarinen,S. Karjalainen,K. O. J. Simola,Pekka Laippala,(unknown)	71
13	The 48,XXYY syndrome: A case detected by maternal serum alpha‐fetoprotein screening 1994 ·Prenatal Diagnosis ·(unknown),(unknown),Riitta Karikoski,K. O. J. Simola	5
14	X‐linked laterality sequence in a family with carrier manifestations 1994 ·American Journal of Medical Genetics ·(unknown),M Janas,Riitta Karikoski,(unknown),K. O. J. Simola	25
15	Molecular cytogenetic study of patients with Pallister-Killian syndrome 1993 ·Human Genetics ·Marcelo L. Larramendy,Mervi Heiskanen,Maija Wessman,Annukka Ritvanen,Païvi Peltomäki,K. O. J. Simola,Helena Kääriäinen,Harriet von Koskull,Marketta Kähkönen,Sakari Knuutila	18
16	A case of human chimerism detected by unbalanced chromosomal translocation 1992 ·Clinical Genetics ·(unknown),(unknown),K. O. J. Simola	13
17	Long-range restriction map around 11p13 aniridia locus 1989 ·Somatic Cell and Molecular Genetics ·Lisa M. Davis,(unknown),K. O. J. Simola,Thomas B. Shows	18
18	Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal aysnapsis 1989 ·Human Genetics ·Riikka Ikonen,Mikael Lindlöf,(unknown),K. O. J. Simola,(unknown),Albert de la Chapelle	8
19	Translocation t(13;14) in nine generations with a case of translocation homozygosity 1988 ·Clinical Genetics ·(unknown),K. O. J. Simola,Markku Ryynänen	7
20	Molecular basis of chromosome banding 1975 ·Chromosoma ·K. O. J. Simola,(unknown),Albert de la Chapelle	4

About K. O. J. Simola

K. O. J. Simola is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 36 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (472 citations), Clinical Biochemistry (100 citations) and Sensory Systems (61 citations). K. O. J. Simola has collaborated with scholars based in Finland, United States and Netherlands. Frequent co-authors include G.A.P. Bruns, Riitta Karikoski, Ilkka Kaitila, Manfred Gessler, Maarit Peippo, Anna Pirkola, Sakari Knuutila, Juha Kere, Leenamaija Pakarinen and Pekka Laippala. Their work appears in journals such as Nature, Science and Proceedings of the National Academy of Sciences.

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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