Barbara Oehl‐Jaschkowitz

1.4k total citations
16 papers, 268 citations indexed

About

Barbara Oehl‐Jaschkowitz is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Barbara Oehl‐Jaschkowitz has authored 16 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Barbara Oehl‐Jaschkowitz's work include Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (5 papers) and Prenatal Screening and Diagnostics (3 papers). Barbara Oehl‐Jaschkowitz is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (5 papers) and Prenatal Screening and Diagnostics (3 papers). Barbara Oehl‐Jaschkowitz collaborates with scholars based in Germany, Poland and United States. Barbara Oehl‐Jaschkowitz's co-authors include Andreas Dufke, Matthias Begemann, Thomas Eggermann, Andreas Tzschach, Manfred Wehrmann, Richard Meyermann, Veronka Horber, Michael Bonin, Rudi Beschorner and Ludwig Aigner and has published in prestigious journals such as The Journal of Pediatrics, Acta Neuropathologica and Orphanet Journal of Rare Diseases.

In The Last Decade

Barbara Oehl‐Jaschkowitz

16 papers receiving 260 citations

Peers

Countries citing papers authored by Barbara Oehl‐Jaschkowitz

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Oehl‐Jaschkowitz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Oehl‐Jaschkowitz. 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 Barbara Oehl‐Jaschkowitz. The network helps show where Barbara Oehl‐Jaschkowitz may publish in the future.

Co-authorship network of co-authors of Barbara Oehl‐Jaschkowitz

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Oehl‐Jaschkowitz. A scholar is included among the top collaborators of Barbara Oehl‐Jaschkowitz 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 Barbara Oehl‐Jaschkowitz. Barbara Oehl‐Jaschkowitz 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:

16 of 16 papers shown

#	Work	Indexed citations
1	The power of the Mediator complex—Expanding the genetic architecture and phenotypic spectrum of MED12‐related disorders 2018 ·Clinical Genetics ·Agnieszka Charzewska, Robert Maiwald, Kimia Kahrizi, Barbara Oehl‐Jaschkowitz, Andreas Dufke, Johannes R. Lemke, H. Enders, Hossein Najmabadi, Andreas Tzschach, (unknown), Corinna Jensen, Melanie Bienek, Jarosław Poznański, Magdalena Nawara, (unknown), Ewa Obersztyn, Dorota Hoffman‐Zacharska, Monika Goś, Jerzy Bal, Vera M. Kalscheuer	17
2	Behavioral and psychological features in girls and women with triple‐X syndrome 2018 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Susann Hänig, Barbara Oehl‐Jaschkowitz, Wolfram Henn, Jobst Meyer	18
3	Dravet syndrome: a new causative SCN 1A mutation? 2017 ·Clinical Case Reports ·Martin Poryo, (unknown), Barbara Oehl‐Jaschkowitz, Alexander Christmann, Ludwig Gortner, Sascha Meyer	4
4	The maternal uniparental disomy of chromosome 6 (upd(6)mat) “phenotype”: result of placental trisomy 6 mosaicism? 2017 ·Molecular Genetics & Genomic Medicine ·Thomas Eggermann, Barbara Oehl‐Jaschkowitz, (unknown), Wolfgang Thomas, Deniz Kanber, Beate Albrecht, Matthias Begemann, Ingo Kurth, Jasmin Beygo, Karin Buiting	18
5	Congenital CLN disease in two siblings 2015 ·Wiener Medizinische Wochenschrift ·Sascha Meyer, Umut Yılmaz, Yoo‐Jin Kim, Robert Steinfeld, G Meyberg-Solomayer, Barbara Oehl‐Jaschkowitz, Andreas Tzschach, Ludwig Gortner, (unknown), O. Schofer	13
6	Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families 2014 ·Orphanet Journal of Rare Diseases ·Naeimeh Tayebi, Aleksander Jamsheer, Ricarda Flöttmann, Anna Sowińska‐Seidler, Sandra C. Doelken, Barbara Oehl‐Jaschkowitz, Wiebke Hülsemann, R. Habenicht, Eva Klopocki, Stefan Mundlos, Malte Spielmann	33
7	Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability 2013 ·American Journal of Medical Genetics Part A ·Barbara Oehl‐Jaschkowitz, Olivier Vanakker, Anne De Paepe, Björn Menten, Thomas G. Martin, Georg F. Weber, Alexander Christmann, (unknown), (unknown), Susan McNerlan, Shane McKee, Andreas Tzschach	17
8	Haploinsufficiency of <b><i>ANKRD11</i></b> (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell Syndrome 2013 ·Molecular Syndromology ·Sabrina Spengler, Barbara Oehl‐Jaschkowitz, Matthias Begemann, (unknown), Klaus Zerres, Thomas Eggermann	10
9	Molecular Karyotyping as a Relevant Diagnostic Tool in Children with Growth Retardation with Silver-Russell Features 2012 ·The Journal of Pediatrics ·Sabrina Spengler, Matthias Begemann, Nadina Ortiz Brüchle, Michael Baudis, Bernd Denecke, (unknown), Barbara Oehl‐Jaschkowitz, Bernd Schulze, (unknown), Christiane Spaich, Peter Blümel, Anna Jauch, Ute Moog, Klaus Zerres, Thomas Eggermann	23
10	Christianson syndrome in a patient with an interstitial Xq26.3 deletion 2011 ·American Journal of Medical Genetics Part A ·Andreas Tzschach, Reinhard Ullmann, (unknown), Thomas G. Martin, Georg F. Weber, (unknown), F. Pauly, Mohammed Ghiath Shamdeen, W. Reith, Barbara Oehl‐Jaschkowitz	11
11	DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith-Wiedemann syndrome 2010 ·Clinical Genetics ·Sascha Tierling, (unknown), Sabine Reither, (unknown), (unknown), Dominique Leitner, Barbara Oehl‐Jaschkowitz, Joern Walter	19
12	Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins 2008 ·American Journal of Medical Genetics Part A ·Bettina Blaumeiser, Barbara Oehl‐Jaschkowitz, Wiktor Borozdin, Jürgen Kohlhase	10
13	Pallister-Killian Syndrome (PKS) as a Cause of Mental Retardation 2008 ·Klinische Pädiatrie ·(unknown), S. Martha Meyer, (unknown), Barbara Oehl‐Jaschkowitz, Ludwig Gortner, Mohammed Ghiath Shamdeen	2
14	Novel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease 2007 ·Neurogenetics ·Ute Hehr, Goekhan Uyanik, Claudia Groß, Maggie C. Walter, Axel Bohring, Monika Cohen, Barbara Oehl‐Jaschkowitz, Lynne M. Bird, (unknown), Ulrich Bogdahn, Gerhard Schuierer, Haluk Topaloğlu, Ludwig Aigner, Hanns Lochmüller, Jürgen Winkler	41
15	Extradural ependymal tumor with myxopapillary and ependymoblastic differentiation in a case of Schinzel–Giedion syndrome 2006 ·Acta Neuropathologica ·Rudi Beschorner, Manfred Wehrmann, (unknown), Michael Bonin, Veronka Horber, Barbara Oehl‐Jaschkowitz, Richard Meyermann, Andreas Dufke	30
16	Kongenitale Muskeldystrophie: Muscle-Eye-Brain disease 2005 ·Klinische Pädiatrie ·(unknown), Tobias Struffert, G. Uyanık, Barbara Oehl‐Jaschkowitz, Ute Hehr, (unknown)	2

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