Maarit Peippo

2.1k total citations
24 papers, 768 citations indexed

About

Maarit Peippo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Maarit Peippo has authored 24 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Maarit Peippo's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maarit Peippo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maarit Peippo collaborates with scholars based in Finland, Germany and Belgium. Maarit Peippo's co-authors include Jaakko Ignatius, Harriet von Koskull, Maria Arvio, Sirpa Ala‐Mello, K. O. J. Simola, Mirja Somer, Juliane Hoyer, Anita Rauch, Christiane Zweier and Alexander Dreweke and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Maarit Peippo

23 papers receiving 747 citations

Peers

Maarit Peippo

GENET

PPCH

SURGE

Dominique Martin‐Coignard France

Matteo Della Monica Italy

Chantal Missirian France

A. Moncla France

Zöe Powis United States

Karen Buysse Belgium

Marzia Pollazzon Italy

I. van der Bürgt Netherlands

Rossella Caselli Italy

Megan T. Cho United States

Dominique Martin‐Coignard France

Maarit Peippo

424 ×0.8

GENET

522 ×1.2

86 ×0.8

78 ×0.8

PPCH

51 ×1.0

SURGE

Citations per year, relative to Maarit Peippo Maarit Peippo (= 1×) peers Dominique Martin‐Coignard

Countries citing papers authored by Maarit Peippo

Since Specialization

Citations

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

Fields of papers citing papers by Maarit Peippo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maarit Peippo

This figure shows the co-authorship network connecting the top 25 collaborators of Maarit Peippo. A scholar is included among the top collaborators of Maarit Peippo 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 Maarit Peippo. Maarit Peippo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sirén, Auli, Kristiina Avela, Mirja Somer, et al.. (2014). X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes. Orphanet Journal of Rare Diseases. 9(1). 49–49. 52 indexed citations

Peippo, Maarit, et al.. (2012). Translation of a Research-Based Genetic Test on a Rare Syndrome into Clinical Service Testing, with Sotos Syndrome As an Example. Genetic Testing and Molecular Biomarkers. 16(10). 1188–1194. 3 indexed citations

Peippo, Maarit & Jaakko Ignatius. (2011). Pitt-Hopkins Syndrome. Molecular Syndromology. 2(3-5). 171–180. 42 indexed citations

Peippo, Maarit, et al.. (2011). 9q22 Deletion - First Familial Case. Orphanet Journal of Rare Diseases. 6(1). 45–45. 8 indexed citations

Peippo, Maarit, et al.. (2009). Weismann‐Netter syndrome and mental retardation: A new patient and review of the literature. American Journal of Medical Genetics Part A. 149A(11). 2593–2601.

Ala‐Mello, Sirpa, et al.. (2008). Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly. American Journal of Medical Genetics Part A. 146A(19). 2490–2494. 28 indexed citations

Zweier, Christiane, Maarit Peippo, Juliane Hoyer, et al.. (2007). Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome). The American Journal of Human Genetics. 80(5). 994–1001. 215 indexed citations

Hoyer, Juliane, Alexander Dreweke, C. Becker, et al.. (2007). Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays. Journal of Medical Genetics. 44(10). 629–636. 56 indexed citations

Peippo, Maarit, Anne M. Koivisto, Teppo Särkämö, et al.. (2007). PAK3 related mental disability: Further characterization of the phenotype. American Journal of Medical Genetics Part A. 143A(20). 2406–2416. 40 indexed citations

10.

Peippo, Maarit, K. O. J. Simola, Leena Valanne, et al.. (2006). Pitt–Hopkins syndrome in two patients and further definition of the phenotype. Clinical Dysmorphology. 15(2). 47–54. 43 indexed citations

11.

Ala‐Mello, Sirpa & Maarit Peippo. (2004). The first Finnish patient with the Floating‐Harbor syndrome: The follow‐up of eight years. American Journal of Medical Genetics Part A. 130A(3). 317–319. 13 indexed citations

12.

Pöyhönen, Minna, et al.. (2004). Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females. Clinical Dysmorphology. 13(2). 85–90. 15 indexed citations

13.

Arvio, Maria, et al.. (2003). Temporo-occipital spikes: a typical EEG finding in Kabuki syndrome. Pediatric Neurology. 30(1). 67–70. 13 indexed citations

14.

Arvio, Maria, et al.. (2003). Dysmorphic facial features in aspartylglucosaminuria patients and carriers. Clinical Dysmorphology. 13(1). 11–15. 10 indexed citations

15.

Mäntyjärvi, Maija, et al.. (2001). Clinical features and a follow‐up study in a family with X‐linked progressive cone‐rod dystrophy. Acta Ophthalmologica Scandinavica. 79(4). 359–365. 17 indexed citations

16.

Arvio, Maria, et al.. (2001). Bone marrow transplantation for aspartylglucosaminuria: Follow-up study of transplanted and non-transplanted patients. The Journal of Pediatrics. 138(2). 288–290. 28 indexed citations

17.

Arvio, Maria, Maarit Peippo, & K. O. J. Simola. (1997). Applicability of a checklist for clinical screening of the fragile X syndrome. Clinical Genetics. 52(4). 211–215. 31 indexed citations

18.

Ranta, Susanna, Anna‐Elina Lehesjoki, Maarit Peippo, & Helena Kääriäinen. (1994). Hemophilia A: Experiences And Attitudes Of Mothers, Sisters, And Daughters. Pediatric Hematology and Oncology. 11(4). 387–397. 14 indexed citations

19.

Oudet, C, et al.. (1993). Striking Founder Effect for the Fragile X Syndrome in Finland. European Journal of Human Genetics. 1(3). 181–189. 48 indexed citations

20.

Somer, Mirja, et al.. (1992). Cardio‐Facio‐Cutaneous syndrome: Three additional cases and review of the literature. American Journal of Medical Genetics. 44(5). 691–695. 24 indexed citations

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.

Explore authors with similar magnitude of impact