Iris Bartels

2.1k total citations
69 papers, 1.3k citations indexed

About

Iris Bartels is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Iris Bartels has authored 69 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Pediatrics, Perinatology and Child Health, 37 papers in Genetics and 14 papers in Molecular Biology. Recurrent topics in Iris Bartels's work include Prenatal Screening and Diagnostics (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Chromosomal and Genetic Variations (13 papers). Iris Bartels is often cited by papers focused on Prenatal Screening and Diagnostics (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Chromosomal and Genetic Variations (13 papers). Iris Bartels collaborates with scholars based in Germany, Poland and United States. Iris Bartels's co-authors include B. Eiben, Barbara Zoll, R. Osmers, I. Hansmann, Martha Hentemann, Peter Burfeind, W. Hammans, A Lindemann, R. Goebel and U. Sancken and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and The Journal of Urology.

In The Last Decade

Iris Bartels

67 papers receiving 1.1k citations

Peers

Countries citing papers authored by Iris Bartels

Since Specialization

Citations

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

Fields of papers citing papers by Iris Bartels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris Bartels

This figure shows the co-authorship network connecting the top 25 collaborators of Iris Bartels. A scholar is included among the top collaborators of Iris Bartels 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 Bartels. Iris Bartels 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	A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation 2021 ·Scientific Reports ·(unknown), (unknown), Stoyan Petkov, (unknown), Anna Maierhofer, (unknown), (unknown), (unknown), Thomas Haaf, Ralf Dressel, Iris Bartels, Rüdiger Behr	9
2	Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22 2018 ·Molecular Cytogenetics ·(unknown), Mateja Smogavec, (unknown), Silke Pauli, Peter Burfeind, Iris Bartels	9
3	Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8 2013 ·Cytogenetic and Genome Research ·Thomas M. Schmidt, Tatjana Bierhals, Fanny Kortüm, Iris Bartels, Thomas Liehr, Peter Burfeind, Moneef Shoukier, Valeska Frank, Carsten Bergmann, Kerstin Kutsche	18
4	Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes 2012 ·European Journal of Medical Genetics ·Silke Pauli, Thomas M. Schmidt, (unknown), Barbara Zoll, Peter Burfeind, (unknown), Moneef Shoukier, Iris Bartels	9
5	A Family with an Inverted Tandem Duplication 5q22.1q23.2 2012 ·Cytogenetic and Genome Research ·Thomas M. Schmidt, Iris Bartels, Thomas Liehr, Peter Burfeind, Barbara Zoll, Moneef Shoukier	15
6	A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect 2011 ·American Journal of Medical Genetics Part A ·Moneef Shoukier, (unknown), (unknown), Iris Bartels, Bernd Auber, Barbara Zoll, Gabriela Salinas, Dagmar Weise, Knut Brockmann, Birgit Zirn, Peter Burfeind	20
7	Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p? 2010 ·Cytogenetic and Genome Research ·Thomas Liehr, Iris Bartels, Barbara Zoll, Elisabeth Ewers, Kristin Mrasek, Nadezda Kosyakova, (unknown), (unknown), Ferdinand von Eggeling, Nicole Posorski, Anja Weise	3
8	Ring chromosome 22 and neurofibromatosis type II: proof of two‐hit model for the loss of the NF2 gene in the development of meningioma 2010 ·Clinical Genetics ·Birgit Zirn, Larissa Arning, Iris Bartels, Moneef Shoukier, Sabine Hoffjan, B Neubauer, (unknown)	31
9	Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation 2009 ·Molecular Cytogenetics ·Bernd Auber, (unknown), Barbara Zoll, Peter Burfeind, (unknown), Thomas Liehr, Knut Brockmann, Ekkehard Wilichowski, (unknown), Iris Bartels	7
10	An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype 2006 ·European Journal of Medical Genetics ·Iris Bartels, Heike Starke, (unknown), Simone M. Sauter, Barbara Zoll, Thomas Liehr	42
11	A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis 2002 ·Cytogenetic and Genome Research ·Ralf Ulrich Trappe, (unknown), Jürgen Kohlhase, Anja Weise, Thomas Liehr, (unknown), Moritz Meins, Barbara Zoll, Iris Bartels, Peter Burfeind	11
12	Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism: Case Report 2001 ·Human Reproduction ·(unknown), Stefan K. Bohlander, Karin Bink, B. Hinney, Franco Laccone, Iris Bartels	12
13	Preliminary data on an association between blood groups and serum markers used for the so-called ?triple screening?: free oestriol MoM values are decreased in rhesus-negative (Rh?) women 2001 ·Prenatal Diagnosis ·U. Sancken, Iris Bartels	6
14	First confirmed case with paternal uniparental disomy of chromosome 16 2000 ·American Journal of Medical Genetics ·(unknown), Bart Janssen, (unknown), Karsten Harms, Iris Bartels	21
15	Normal Outcome of a Pregnancy with Mosaicism for Double Trisomy in Amniotic Fluid cells 1997 ·Prenatal Diagnosis ·Iris Bartels, Ulrich Franke, (unknown), R. Rauskolb, (unknown)	1
16	Prenatal detection of X‐linked ichthyosis by maternal serum screening for down syndrome 1994 ·Prenatal Diagnosis ·Iris Bartels, (unknown), U. Sancken	26
17	Simultaneous placentacentesis and amniocentesis for prenatal karyotyping: Report on 250 cases 1990 ·Prenatal Diagnosis ·(unknown), R. Rauskolb, (unknown), (unknown), B. Eiben, Iris Bartels	3
18	Excess of females in chromosomally normal spontaneous abortuses 1990 ·American Journal of Medical Genetics ·Iris Bartels, I. Hansmann, B. Eiben	20
19	Abnormal pregnancy sonogram and chromosomal anomalies: Four years' experience with rapid karyotyping 1989 ·Prenatal Diagnosis ·Martha Hentemann, R. Rauskolb, R. G. Ulbrich, Iris Bartels	16
20	Down syndrome at birth not detected by first‐trimester chorionic villus sampling 1989 ·American Journal of Medical Genetics ·Iris Bartels, I. Hansmann, (unknown), Barbara Zoll, R. Rauskolb	13

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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