Tuula Rinne

3.7k citations

32 papers · 997 indexed · h-index 15

Impact in

Neurology top 5%
- Vestibular and auditory disorders
Oncology top 10%
- Cancer-related Molecular Pathways

Papers in

Urology 4
- Urological Disorders and Treatments 4
Sensory Systems 3
- Hearing, Cochlea, Tinnitus, Genetics 3

Co-authors: Hans van Bokhoven H.G. Brunner Han G. Brunner M. A. Gresty Adolfo M. Bronstein Linda Luxon Peter Rudge Ben C.J. Hamel
Journals: European Journal of Human Genetics (2 papers)International Journal of Molecular Sciences (2 papers)Journal of Medical Genetics (2 papers)Scientific Reports (1 paper)Nature Genetics (1 paper)
Partner nations: Netherlands United States Italy

In The Last Decade

Tuula Rinne

30 papers receiving 984 citations

Peers

Countries citing papers authored by Tuula Rinne

Since Specialization

Citations

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

Fields of papers citing papers by Tuula Rinne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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

20 of 20 papers shown

#	Work
1	Nerve enlargement in patients with Noonan syndrome: A retrospective cohort study American Journal of Medical Genetics Part A ·JM Ramos Rodríguez, Erika Leenders, Corrie E. Erasmus, Hilde M. H. Braakman, Melissa Guadalupe Sagal Bustamante, 耕一郎山崎, Tuula Rinne, Martin Zenker, Marco Tartaglia, J S Kim, Nicol C. Voermans, Baziel G.M. van Engelen, Nens van Alfen, Jos Draaisma	2024	0
2	Hypertrophic neuropathy: a possible cause of pain in children with Noonan syndrome and related disorders European Journal of Pediatrics ·JM Ramos Rodríguez, Corrie E. Erasmus, Hilde M. H. Braakman, Melissa Guadalupe Sagal Bustamante, Erika Leenders, Tuula Rinne, Nens van Alfen, Jos Draaisma	2023	2
3	Lessons Learned from 17 Years of Multidisciplinary Care for Differences of Sex Development Patients at a Single Indonesian Center Sexual Development ·Sultana MH Faradz, O. Shoham, Agustini Utari, Maia Farrugia Wismayer, Achmad Zulfa Juniarto, Santa Ohga, Annastasia Ediati, Tuula Rinne, Dineke Westra, Hedi L. Claahsen‐van der Grinten, Frank H. de Jong, Stenvert L. S. Drop, Katie Ayers, Andrew Sinclair	2023	2
4	Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country Frontiers in Endocrinology ·Agustini Utari, Sultana MH Faradz, Annastasia Ediati, Tuula Rinne, Maia Farrugia Wismayer, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen‐van der Grinten	2022	5
5	TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility European Journal of Human Genetics ·Е Н Полянская, Erika Leenders, Misato Shiromaru, Pauline Terhal, Katharina Löhner, Bert B.A. de Vries, Trijnie Dijkhuizen, Yvonne J. Vos, Tuula Rinne, Maarten P. van den Berg, Sourav Kumar, Patrick Deelen, Conny M.A. van Ravenswaaij‐Arts, Wilhelmina S. Kerstjens‐Frederikse	2021	15
6	Under-reported aspects of diagnosis and treatment addressed in the Dutch-Flemish guideline for comprehensive diagnostics in disorders/differences of sex development Journal of Medical Genetics ·Yolande van Bever, Hennie T. Brüggenwirth, Katja P. Wolffenbuttel, Arianne B. Dessens, Irene A.L. Groenenberg, Maarten F. C. M. Knapen, Elfride De Baere, Martine Cools, Conny M.A. van Ravenswaaij‐Arts, Birgit Sikkema‐Raddatz, Hedi L. Claahsen‐van der Grinten, Marlies Kempers, Tuula Rinne, Remko Hersmus, Leendert H. J. Looijenga, Sabine E Hannema	2020	10
7	Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder The American Journal of Human Genetics ·Susan M. Hiatt, Michelle L. Thompson, Jeremy W. Prokop, James M.J. Lawlor, Stacy W. Gray, E. Martina Bebin, Tuula Rinne, Marlies Kempers, Rolph Pfundt, Bregje W.M. van Bon, Cyril Mignot, Caroline Nava, Christel Depienne, Louisa Kalsner, Anita Rauch, Pascal Joset, Ruxandra Bachmann‐Gagescu, Ingrid M. Wentzensen, Kirsty McWalter, Gregory M. Cooper	2019	15
8	Oculoectodermal Syndrome – Encephalocraniocutaneous Lipomatosis Associated with NRAS Mutation Acta Dermato Venereologica ·Krishanu Prakash, Marieke M.B. Seyger, Negm el-Din Mohammed Sherif, Tuula Rinne, Astrid Eijkelenboom, Michèl A.A.P. Willemsen	2019	7
9	AB0090 INHERITED DEFICIT OF PROTEOGLYCAN MIMICKING SEPTIC ARTHRITIS Annals of the Rheumatic Diseases ·香青木, Riccardo Papa, Roberta Caorsi, Alessandro Consolaro, Roberto Gastaldi, Angelo Ravelli, Marco Gattorno, Paolo Picco, Tuula Rinne	2019	2
10	Functional characterisation of a novel class of in-frame insertion variants of KRAS and HRAS Scientific Reports ·Astrid Eijkelenboom, F.M.A. van Schaik, Robert M. van Es, Roel W. Ten Broek, Tuula Rinne, Carine van der Vleuten, Uta Flucke, Marjolijn J. L. Ligtenberg, Holger Rehmann	2019	8
11	De novo mutations in theSETnuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disability Human Mutation ·Servi J.C. Stevens, Vyne van der Schoot, Magalie S. Leduc, Tuula Rinne, Seema R. Lalani, Marjan M. Weiss, Johanna M. van Hagen, Augusta M.A. Lachmeijer, (unknown), Sylvia Stöckler‐Ipsiroglu, Anna Lehman, Han G. Brunner	2018	14
12	The Immune Phenotype of Patients with CHARGE Syndrome The Journal of Allergy and Clinical Immunology In Practice ·Peter Hsu, Alan Ma, Elizabeth H Barnes, Meredith Wilson, Lies H. Hoefsloot, Tuula Rinne, Craig F. Munns, Нечепуренко Александр Васильевич, Melanie Wong, Sam Mehr	2015	13
13	Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon‐ectodermal defects‐cleft lip/palate syndrome (AEC) American Journal of Medical Genetics Part A ·Tuula Rinne, Emine Bolat, Prabala Ramamurty, Hans Scheffer, Hans van Bokhoven	2009	43
14	Limb‐mammary syndrome (LMS) associated with internal female genitalia dysgenesia: A new genotype/phenotype correlation? American Journal of Medical Genetics Part A ·Laura Guazzarotti, Haranoshiro Sho, Tuula Rinne, Peng Kong, Rita Machacy, 人見秀, Sebastiaan Platvoet, Hans van Bokhoven, Gianvincenzo Zuccotti	2008	16
15	Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association) Wiener klinische Wochenschrift ·Gerda Hofstetter, Nicole Concin, Christian Marth, Tuula Rinne, Martin Erdel, Andreas Janecke	2008	11
16	A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes Human Molecular Genetics ·Tuula Rinne, L. Raki, Evert N. Lamme, Pascal H. G. Duijf, Emine Bolat, Rowdy Meijer, Hans Scheffer, Elisabeth Rosser, Tiong Yang Tan, John A. McGrath, Joost Schalkwijk, H.G. Brunner, Huiqing Zhou, Hans van Bokhoven	2008	46
17	p63-Associated Disorders Cell Cycle ·Tuula Rinne, H.G. Brunner, Hans van Bokhoven	2007	222
18	Pattern of p63 mutations and their phenotypes—update American Journal of Medical Genetics Part A ·Tuula Rinne, Ben C.J. Hamel, Hans van Bokhoven, Han G. Brunner	2006	120
19	Bilateral loss of vestibular function: clinical findings in 53 patients Journal of Neurology ·Tuula Rinne, Adolfo M. Bronstein, Peter Rudge, M. A. Gresty, Linda Luxon	1998	123
20	Bilateral Loss of Vestibular Function Acta Oto-Laryngologica ·Tuula Rinne, Adolfo M. Bronstein, Peter Rudge, M. A. Gresty, Linda Luxon	1995	36

About Tuula Rinne

Tuula Rinne is a scholar working on Urology, Sensory Systems, Oncology, Genetics and Molecular Biology, having authored 32 papers that have together received 997 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (7 papers), Protein Tyrosine Phosphatases (7 papers), Cancer-related Molecular Pathways (7 papers), RNA modifications and cancer (5 papers), Galectins and Cancer Biology (5 papers), Sexual Differentiation and Disorders (4 papers), Urological Disorders and Treatments (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). The work is most often cited by research in Neurology (151 citations), Oncology (379 citations), Sensory Systems (60 citations), Developmental Biology (25 citations) and Genetics (253 citations). Tuula Rinne has collaborated with scholars based in Netherlands, United States and Italy. Frequent co-authors include Hans van Bokhoven, H.G. Brunner, Han G. Brunner, M. A. Gresty, Adolfo M. Bronstein, Linda Luxon, Peter Rudge, Ben C.J. Hamel, Hans Scheffer and Emine Bolat. Their work appears in journals such as European Journal of Human Genetics, International Journal of Molecular Sciences, Journal of Medical Genetics, Scientific Reports and Nature Genetics.

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