Iris Marquardt

1.9k total citations
15 papers, 796 citations indexed

About

Iris Marquardt is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, Iris Marquardt has authored 15 papers receiving a total of 796 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 3 papers in Cell Biology. Recurrent topics in Iris Marquardt's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Trace Elements in Health (3 papers). Iris Marquardt is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Trace Elements in Health (3 papers). Iris Marquardt collaborates with scholars based in Germany, United States and Netherlands. Iris Marquardt's co-authors include Jens Frahm, F. Hanefeld, Wolfgang Hänicke, U. Holzbach, Gunther Helms, Sylvia Stöckler, Georg Christoph Korenke, Ulrike Steuerwald, Stefanie Sander and Johannes Sander and has published in prestigious journals such as PEDIATRICS, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Iris Marquardt

15 papers receiving 775 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Iris Marquardt Germany	11	401	347	225	149	120	15	796
Ángela Arias Spain	18	278 0.7×	290 0.8×	237 1.1×	104 0.7×	146 1.2×	31	673
Carla Carducci Italy	17	818 2.0×	948 2.7×	221 1.0×	140 0.9×	216 1.8×	47	1.5k
M. Rimoldi Italy	21	892 2.2×	1.2k 3.3×	73 0.3×	133 0.9×	213 1.8×	58	1.6k
Stéphanie Gobin France	16	321 0.8×	432 1.2×	67 0.3×	58 0.4×	95 0.8×	27	778
I. E. M. Luyt‐Houwen Netherlands	14	564 1.4×	866 2.5×	70 0.3×	50 0.3×	120 1.0×	26	1.1k
Eddie O’Gorman Switzerland	10	132 0.3×	408 1.2×	199 0.9×	36 0.2×	158 1.3×	10	676
Paula Garcia Portugal	16	272 0.7×	344 1.0×	40 0.2×	106 0.7×	162 1.4×	49	774
K. Bartholomé Germany	16	636 1.6×	441 1.3×	92 0.4×	119 0.8×	181 1.5×	27	931
K Naess Sweden	15	466 1.2×	740 2.1×	29 0.1×	47 0.3×	117 1.0×	41	974
Alex E. Felice Malta	16	73 0.2×	270 0.8×	68 0.3×	53 0.4×	153 1.3×	59	1.0k

Countries citing papers authored by Iris Marquardt

Since Specialization

Citations

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

Fields of papers citing papers by Iris Marquardt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris Marquardt

This figure shows the co-authorship network connecting the top 25 collaborators of Iris Marquardt. A scholar is included among the top collaborators of Iris Marquardt 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 Iris Marquardt. Iris Marquardt 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:

15 of 15 papers shown

1.

Meinecke, Peter, Iris Marquardt, Malik Alawi, et al.. (2020). Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities. The American Journal of Human Genetics. 107(6). 1044–1061. 14 indexed citations

2.

Castiglia, Lucia, Ralf A. Husain, Iris Marquardt, et al.. (2017). 7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder. Journal of Intellectual Disability Research. 62(5). 359–370. 3 indexed citations

3.

Kortüm, Fanny, Iris Marquardt, Malik Alawi, et al.. (2016). Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate Phenotype. PEDIATRICS. 139(1). 22 indexed citations

4.

Baumann, Matthias, Kathrin Schanda, Michael Karenfort, et al.. (2016). Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases. Multiple Sclerosis Journal. 22(14). 1821–1829. 104 indexed citations

5.

Baumann, Matthias, E. Hennes, Kathrin Schanda, et al.. (2015). OP65 – 3006: Clinical characteristics and neuroradiological findings in children with multiphasic demyelinating encephalomyelitis and MOG antibodies. European Journal of Paediatric Neurology. 19. S21–S21. 1 indexed citations

6.

Huppke, Peter, Cornelia Brendel, Vera M. Kalscheuer, et al.. (2012). Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin. The American Journal of Human Genetics. 90(1). 61–68. 68 indexed citations

7.

Huppke, Peter, Cornelia Brendel, Vera M. Kalscheuer, et al.. (2012). Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin. The American Journal of Human Genetics. 90(2). 378–378. 3 indexed citations

8.

Huppke, Peter, Cornelia Brendel, Georg Christoph Korenke, et al.. (2012). Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase. Human Mutation. 33(8). 1207–1215. 29 indexed citations

9.

Heldt, Katrin, Bernd Schwahn, Iris Marquardt, Marissa Grotzke, & U. Wendel. (2005). Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxification. Molecular Genetics and Metabolism. 84(4). 313–316. 26 indexed citations

10.

Sander, Johannes, Stefanie Sander, Ulrike Steuerwald, et al.. (2005). Neonatal screening for defects of the mitochondrial trifunctional protein. Molecular Genetics and Metabolism. 85(2). 108–114. 56 indexed citations

11.

Ensenauer, Regina, Jerry Vockley, Jörn Oliver Sass, et al.. (2004). A Common Mutation Is Associated with a Mild, Potentially Asymptomatic Phenotype in Patients with Isovaleric Acidemia Diagnosed by Newborn Screening. The American Journal of Human Genetics. 75(6). 1136–1142. 100 indexed citations

12.

Korenke, GC, et al.. (2004). Defekt der langkettigen 3-Hydroxy-Acyl-CoA-Dehydrogenase—LCHAD-Defekt. Monatsschrift Kinderheilkunde. 153(7). 657–663. 1 indexed citations

13.

Sander, Johannes, Nils Janzen, Stefanie Sander, et al.. (2003). Neonatal screening for citrullinaemia. European Journal of Pediatrics. 162(6). 417–420. 32 indexed citations

14.

Coenen, Marieke J. H., Leo Nijtmans, Éva Morava, et al.. (1999). SURFEIT-1 Gene Analysis and Two-Dimensional Blue Native Gel Electrophoresis in Cytochrome c Oxidase Deficiency. Biochemical and Biophysical Research Communications. 265(2). 339–344. 46 indexed citations

15.

Stöckler, Sylvia, U. Holzbach, F. Hanefeld, et al.. (1994). Creatine Deficiency in the Brain: A New, Treatable Inborn Error of Metabolism. Pediatric Research. 36(3). 409–413. 291 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.

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