Katharina Schoner

513 citations

20 papers · 272 indexed · h-index 10

Co-authors: Helga Rehder Bárbara Fritz Jens Figiel J Steinhard R. Bald Britta Kluge J. Kunz Johannes Zschocke
Topics: Prenatal Screening and Diagnostics (5 papers)Connective tissue disorders research (3 papers)Genetic and Kidney Cyst Diseases (3 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Rheumatology
Journals: Journal of Bone and Mineral Research Obstetrics and Gynecology European Journal of Human Genetics
Partner nations: Germany Austria United States

In The Last Decade

Katharina Schoner

19 papers receiving 256 citations

Peers

Countries citing papers authored by Katharina Schoner

Since Specialization

Citations

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

Fields of papers citing papers by Katharina Schoner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katharina Schoner

This figure shows the co-authorship network connecting the top 25 collaborators of Katharina Schoner. A scholar is included among the top collaborators of Katharina Schoner 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 Katharina Schoner. Katharina Schoner 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	Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one case 2024 ·Orphanet Journal of Rare Diseases ·(unknown),Helga Rehder,(unknown),Christine Bärtsch,Bárbara Fritz,Cordula Knopp,(unknown),(unknown),(unknown),R Axt-Fliedner,(unknown),Manuel Höfer,Franco Laccone,Katharina Schoner	0
2	Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations 2023 ·Orphanet Journal of Rare Diseases ·Helga Rehder,Susanne Gerit Kircher,Katharina Schoner,Mateja Smogavec,(unknown),(unknown),(unknown),Manuel Höfer,Helmut Ringl,Franco Laccone	2
3	Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain 2021 ·European Journal of Human Genetics ·(unknown),Ilona Krey,(unknown),Rami Abou Jamra,Tobias Bartolomaeus,(unknown),Steffen Syrbe,(unknown),(unknown),Christian Roth,Helga Rehder,(unknown),Diana Le Duc,Susanna Schubert,(unknown),Alejandro Leal,Katharina Schoner,Bernt Popp	2
4	Compound Heterozygous Frameshift Mutations in MESD Cause a Lethal Syndrome Suggestive of Osteogenesis Imperfecta Type XX 2020 ·Journal of Bone and Mineral Research ·Julian Stürznickel,Katharina Jähn,Jozef Zustin,(unknown),(unknown),Katharina Schoner,Helga Rehder,Alfons Kreczy,Thorsten Schinke,Michael Amling,Uwe Kornak,Ralf Oheim	13
5	Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern 2019 ·Birth Defects Research ·Katharina Schoner,Martina Witsch‐Baumgartner,(unknown),(unknown),R. Bald,Susanne Gerit Kircher,Annette Ramaswamy,Britta Kluge,(unknown),Ralf Schmitz,Bárbara Fritz,Johannes Zschocke,Franco Laccone,Helga Rehder	14
6	Hypomorphic mutations of TRIP11 cause odontochondrodysplasia 2019 ·JCI Insight ·(unknown),Tomasz M. Witkos,Sheila Unger,(unknown),John A. Follit,Johannes C. Hermann,Tim J. M. Welting,Virginia Fano,Marja Hietala,Nithiwat Vatanavicharn,Katharina Schoner,Jürgen W. Spranger,Miriam Schmidts,Bernhard Zabel,Gregory J. Pazour,Agnès Bloch‐Zupan,Gen Nishimura,Andrea Superti‐Furga,Martin Lowe,Ekkehart Lausch	61
7	Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB‐related skeletal disorders in three fetuses and a 106‐year‐old exhibit 2018 ·American Journal of Medical Genetics Part A ·Helga Rehder,Franco Laccone,Susanne Gerit Kircher,Ralf L. Schild,(unknown),R. Bald,(unknown),(unknown),Jürgen Neesen,Katharina Schoner	2
8	Actin isoform expression patterns in adult extracardiac and cardiac rhabdomyomas indicate a different cell of origin 2017 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·(unknown),Katharina Schoner,Sylvia Hartmann,Andreas M. Sesterhenn,Roland Moll	2
9	Fetal Pathology of Neural Tube Defects – An Overview of 68 Cases 2017 ·Geburtshilfe und Frauenheilkunde ·Katharina Schoner,R Axt-Fliedner,R. Bald,Bárbara Fritz,(unknown),Thomas Kohl,Helga Rehder	14
10	Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel–Manzke syndrome in a fetus 2017 ·American Journal of Medical Genetics Part A ·Katharina Schoner,R. Bald,Denise Horn,Helga Rehder,Uwe Kornak,Nadja Ehmke	6
11	Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing 2015 ·Molecular and Cellular Probes ·Cordula Knopp,Sabine Rudnik‐Schöneborn,Thomas Eggermann,Carsten Bergmann,Matthias Begemann,Katharina Schoner,Klaus Zerres,Nadina Ortiz Brüchle	21
12	Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosity 2012 ·Prenatal Diagnosis ·Helga Rehder,Katharina Schoner,Britta Kluge,Frank Louwen,E. Schwinger,Jürgen Neesen	8
13	Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. – Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele 2012 ·Prenatal Diagnosis ·Katharina Schoner,(unknown),Annette Müller,Thomas Schramm,(unknown),Ralf Schmitz,Jürgen Neesen,P. Wieacker,Helga Rehder	25
14	Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene 2011 ·European Journal of Human Genetics ·Franco Laccone,Katharina Schoner,Birgit Krabichler,Britta Kluge,(unknown),(unknown),Johannes Zschocke,Helga Rehder	21
15	Recurrent Johanson-Blizzard Syndrome in a Triplet Pregnancy Complicated by Urethral Obstruction Sequence: A Clinical, Molecular, and Immunohistochemical Approach 2011 ·Pediatric and Developmental Pathology ·Katharina Schoner,Bárbara Fritz,(unknown),Frank Louwen,Martin Zenker,Roland Moll,Helga Rehder	3
16	Tetrasomy 12p (Pallister-Killian syndrome): difficulties in prenatal diagnosis 2009 ·Archives of Gynecology and Obstetrics ·J. Kunz,Katharina Schoner,W Stein,Helga Rehder,Bárbara Fritz	22
17	Fetal Manifestation of the Fine-Lubinsky Syndrome 2008 ·Fetal Diagnosis and Therapy ·Katharina Schoner,R. Bald,Bárbara Fritz,Helga Rehder	3
18	Severe Facial Clefts in Acrofacial Dysostosis 2008 ·Obstetrics and Gynecology ·Katharina Schoner,J Steinhard,Jens Figiel,Helga Rehder	29
19	A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel–Gruber syndrome 2007 ·Clinical Genetics ·Bernd Auber,Peter Burfeind,Sabine Herold,Katharina Schoner,Gabrielle Gold‐von Simson,R. Rauskolb,Helga Rehder	17
20	Foudroyanter Verlauf einer Malaria tropica 2001 ·DMW - Deutsche Medizinische Wochenschrift ·Steffen Lamparter,Katharina Schoner,Rachel Moll,H. D. Mennel,B Maisch	7

About Katharina Schoner

Katharina Schoner is a scholar working on Genetics, Transplantation and Pediatrics, Perinatology and Child Health, having authored 20 papers that have together received 272 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Connective tissue disorders research (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Genetics (127 citations), Pediatrics, Perinatology and Child Health (66 citations) and Rheumatology (31 citations). Katharina Schoner has collaborated with scholars based in Germany, Austria and United States. Frequent co-authors include Helga Rehder, Bárbara Fritz, Jens Figiel, J Steinhard, R. Bald, Britta Kluge, J. Kunz, Johannes Zschocke, Franco Laccone and Ralf Schmitz. Their work appears in journals such as Journal of Bone and Mineral Research, Obstetrics and Gynecology and European Journal of Human 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.

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