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Frits A. Wijburg

ResearcherPublications, citations & collaboration network

Frits A. Wijburg is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Frits A. Wijburg have?

ScholarIQindexed works

Frits A. Wijburg has 413 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Frits A. Wijburg have?

ScholarIQcitation count

Frits A. Wijburg has 19,169 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Frits A. Wijburg?

ScholarIQh-index

Frits A. Wijburg has an h-index of 73 in OpenAlex.

What is the i10-index of Frits A. Wijburg?

ScholarIQi10-index

Frits A. Wijburg has an i10-index of 235 in OpenAlex.

What is the ORCID of Frits A. Wijburg?

ScholarIQorcid

The ORCID for Frits A. Wijburg is on the source record.

What is the OpenAlex record for Frits A. Wijburg?

ScholarIQopenalex

The OpenAlex for Frits A. Wijburg is on the source record.

What are the most-cited papers on Frits A. Wijburg?

ScholarIQmost cited works
Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia
Matthias R. Baumgartner, Friederike Hörster, Carlo Dionisi‐Vici, Göknur Haliloğlu, Daniela Karall, Kimberly A. Chapman, Martina Huemer, Michel Hochuli, Murielle Assoun, Diana Ballhausen, Alberto Burlina, Brian Fowler, Sarah C. Grünert, Stephanie Grünewald, Tomáš Honzík, B. Merinero, Celia Pérez‐Cerdá, Sabine Scholl‐Bürgi, Flemming Skovby, Frits A. Wijburg, Anita MacDonald, Diego Martinelli, Jörn Oliver Sass, Vassili Valayannopoulos, Anupam Chakrapani
Orphanet Journal of Rare Diseases. 2014728 CitationsOPEN ACCESS
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document
Marieke Biegstraaten, Reynir Arngrı́msson, Frédéric Barbey, Lut Boks, Franco Cecchi, Patrick Deegan, Ulla Feldt‐Rasmussen, Tarekegn Geberhiwot, Dominique P. Germain, Christian J. Hendriksz, Derralynn Hughes, Ilkka Kantola, Nesrin Karabul, Christine Lavery, Gabor E. Linthorst, Atul Mehta, Erica van de Mheen, João Paulo Oliveira, Rossella Parini, Uma Ramaswami, Michael Rudnicki, Andreas L. Serra, Claudia Sommer, Gere Sunder–Plassmann, Einar Svarstad, Annelies Sweeb, Wim Terryn, Anna Tylki‐Szymańska, Camilla Tøndel, Bojan Vujkovac, Frank Weidemann, Frits A. Wijburg, Peter Woolfson, Carla E. M. Hollak
Orphanet Journal of Rare Diseases. 2015347 CitationsOPEN ACCESS
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
Stefan Kölker, Ángeles García Cazorla, Vassili Valayannopoulos, Allan M. Lund, Alberto Burlina, Jolanta Sykut‐Cegielska, Frits A. Wijburg, Elisa Leão Teles, Jiri Zeman, Carlo Dionisi‐Vici, Ivo Barić, Daniela Karall, Persephone Augoustides‐Savvopoulou, Lise Aksglæde, Jean‐Baptiste Arnoux, Paula Avram, Matthias R. Baumgartner, Javier Blasco‐Alonso, B. Chabrol, Anupam Chakrapani, Kimberly A. Chapman, Elisenda Cortès i Saladelafont, María L. Couce, Linda De Meırleır, Dries Dobbelaere, Veronika Dvořáková, Francesca Furlan, Florian Gleich, Wanda Gradowska, Stephanie Grünewald, Anil Jalan, Johannes Häberle, Gisela Haege, Robin Lachmann, Alexander Laemmle, Eveline J. Langereis, Pascale de Lonlay, Diego Martinelli, Shirou Matsumoto, Chris Mühlhausen, Hélène Ogier de Baulny, C. Ortez, Luis Peña Quintana, Danijela Petković Ramadža, Esmeralda Rodrigues, Sabine Scholl‐Bürgi, Étienne Sokal, Christian Staufner, Marshall Summar, Nicholas J. Thompson, Roshni Vara, Inmaculada Vives Piñera, John H. Walter, Monique Williams, Peter Burgard
Journal of Inherited Metabolic Disease. 2015253 CitationsOPEN ACCESS
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
Stefan Kölker, Vassili Valayannopoulos, Alberto Burlina, Jolanta Sykut‐Cegielska, Frits A. Wijburg, Elisa Leão Teles, Jiri Zeman, Carlo Dionisi‐Vici, Ivo Barić, Daniela Karall, Jean‐Baptiste Arnoux, Paula Avram, Matthias R. Baumgartner, Javier Blasco‐Alonso, S. P. Nikolas Boy, Malene Bøgehus Rasmussen, Peter Burgard, B. Chabrol, Anupam Chakrapani, Kimberly A. Chapman, Elisenda Cortès i Saladelafont, María L. Couce, Linda De Meırleır, Dries Dobbelaere, Francesca Furlan, Florian Gleich, Marı́a Julieta González, Wanda Gradowska, Stephanie Grünewald, Tomáš Honzík, Friederike Hörster, Hariklea Ioannou, Anil Jalan, Johannes Häberle, Gisela Haege, Eveline J. Langereis, Pascale de Lonlay, Diego Martinelli, Shirou Matsumoto, Chris Mühlhausen, Elaine Murphy, Hélène Ogier de Baulny, C. Ortez, Consuelo Pedrón, Guillem Pintos‐Morell, Luis Peña Quintana, Danijela Petković Ramadža, Esmeralda Rodrigues, Sabine Scholl‐Bürgi, Étienne Sokal, Marshall Summar, Nicholas J. Thompson, Roshni Vara, Inmaculada Vives Piñera, John H. Walter, Monique Williams, Allan M. Lund, Ángeles García Cazorla
Journal of Inherited Metabolic Disease. 2015239 CitationsOPEN ACCESS
Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure
Minke H. de Ru, Jaap Jan Boelens, Anibh M. Das, Simon Jones, Johanna H. van der Lee, Nizar Mahlaoui, Eugen Mengel, Martin Offringa, Anne O’Meara, Rossella Parini, Attilio Rovelli, Karl‐Walter Sykora, Vassili Valayannopoulos, Ashok Vellodi, Robert Wynn, Frits A. Wijburg
Orphanet Journal of Rare Diseases. 2011234 CitationsOPEN ACCESS

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