Susanne Morlot

2.2k total citations
35 papers, 960 citations indexed

About

Susanne Morlot is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Susanne Morlot has authored 35 papers receiving a total of 960 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 18 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Susanne Morlot's work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (5 papers) and BRCA gene mutations in cancer (4 papers). Susanne Morlot is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (5 papers) and BRCA gene mutations in cancer (4 papers). Susanne Morlot collaborates with scholars based in Germany, United Kingdom and United States. Susanne Morlot's co-authors include Stefan Mundlos, Kerstin Kutsche, Katarina Lehmann, Oliver Bartsch, E Seemanová, Stefanie Schmidt, Peter Wieacker, Susanne Ledig, Timm O. Goecke and Olaf Hiort and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Susanne Morlot

34 papers receiving 932 citations

Peers

Countries citing papers authored by Susanne Morlot

Since Specialization

Citations

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

Fields of papers citing papers by Susanne Morlot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanne Morlot

This figure shows the co-authorship network connecting the top 25 collaborators of Susanne Morlot. A scholar is included among the top collaborators of Susanne Morlot 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 Susanne Morlot. Susanne Morlot 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	Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German‐speaking countries 2024 ·Journal of Inherited Metabolic Disease ·Anibh M. Das, Diana Ballhausen, Dorothea Haas, Johannes Häberle, (unknown), (unknown), Nils Janzen, Johannes Sander, Peter Freisinger, Daniela Karall, Uta Meyer, E. Mönch, Susanne Morlot, (unknown), Sabine Scholl‐Bürgi, Stephan vom Dahl, Natalie Weinhold, Jiri Zeman, Karin Lange	3
2	OnkoRiskNET: a multicenter, interdisciplinary, telemedicine-based model to improve care for patients with a genetic tumor risk syndrome 2022 ·BMC Health Services Research ·(unknown), (unknown), Susanne Morlot, (unknown), (unknown), Elena Link, Eva Baumann, (unknown), Evelin Schröck, Anke K. Bergmann, Brigitte Schlegelberger	2
3	De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia 2020 ·Clinical Genetics ·(unknown), (unknown), Susanne Morlot, Gunnar Schmidt, Bernd Auber, (unknown), Gudrun Göhring, Tim Ripperger, Brigitte Schlegelberger, Winfried Hofmann, Thomas Smol, Emilie Ait‐Yahya, Anna Raimbault, Anne Lambilliotte, Florence Petit, Doris Steinemann	5
4	Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A 2019 ·American Journal of Medical Genetics Part A ·Monika M. Golas, Bernd Auber, Tim Ripperger, Brigitte Pabst, Gunnar Schmidt, Michel Morlot, (unknown), Doris Steinemann, Brigitte Schlegelberger, Susanne Morlot	9
5	A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome 2018 ·Breast Cancer Research and Treatment ·(unknown), (unknown), Barbara Wappenschmidt, (unknown), Brigitte Pabst, Saki Chan, Han Cao, Susanne Morlot, Caroline Scholz, Bernd Auber, Kerstin Rhiem, Rita K. Schmutzler, Thomas Illig, Brigitte Schlegelberger, Doris Steinemann	11
6	12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature 2018 ·European Journal of Medical Genetics ·(unknown), (unknown), Tim Ripperger, Susanne Morlot, Thomas Illig, Thomas Eggermann, Brigitte Schlegelberger, Caroline Scholz, Doris Steinemann	7
7	Premature Ovarian Failure Caused by a Heterozygous Missense Mutation in <b><i>POF1B</i></b> and a Reciprocal Translocation 46,X,t(X;3)(q21.1;q21.3) 2015 ·Sexual Development ·Susanne Ledig, Sabine Preisler-Adams, Susanne Morlot, Thomas Liehr, P. Wieacker	9
8	Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin 2012 ·Molecular Syndromology ·Mahdi Ghani, Peter N. Robinson, Susanne Morlot, Diana Mitter, Marc Trimborn, (unknown), Raymonda Varon, Karl Sperling, Heidemarie Neitzel	15
9	Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutation 2011 ·Human Mutation ·J. Vogt, (unknown), Susanne Morlot, Lan Kluwe, (unknown), D.N. Cooper, Hildegard Kehrer‐Sawatzki	22
10	Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci 2010 ·Human Reproduction ·Susanne Ledig, Olaf Hiort, Gerd Scherer, Michael J. Hoffmann, G. Wolff, Susanne Morlot, A. Kuechler, Peter Wieacker	72
11	8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families 2010 ·Molecular Cytogenetics ·John Barber, (unknown), (unknown), (unknown), Susanne Morlot, (unknown), Thomas Liehr, Cláudia Alves, Joana Trindade, (unknown), (unknown), (unknown), (unknown), Viv Maloney	23
12	Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome 2010 ·European Journal of Medical Genetics ·(unknown), Bettina Bohnhorst, I. Luhmer, Susanne Morlot, Axel Bohring, Jon Jonasson, Jörg T. Epplen, Dorothea Gadzicki, Stefanie Glaser, Gudrun Göhring, (unknown), Anke Hein, Mine Arslan‐Kirchner, Manfred Stuhrmann, Jörg Schmidtke, Brigitte Pabst	14
13	Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation 2009 ·Human Molecular Genetics ·Lothar Gremer, Alessandro De Luca, Torsten Merbitz-Zahradnik, Bruno Dallapiccola, Susanne Morlot, Marco Tartaglia, Kerstin Kutsche, Mohammad Reza Ahmadian, Georg Rosenberger	32
14	10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences 2009 ·Cytogenetic and Genome Research ·Thomas Liehr, Markus Stümm, R.‐D. Wegner, Samarth Bhatt, (unknown), Philippos C. Patsalis, Moritz Meins, Susanne Morlot, (unknown), Elisabeth Ewers, Sophie Hinreiner, Kristin Mrasek, Nadezda Kosyakova, (unknown), Sau Wai Cheung, Anja Weise	27
15	Sprachentwicklungsstörung bei Mosaik-Trisomie 8 2009 ·HNO ·M. Ptok, Susanne Morlot	1
16	A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN 2007 ·The American Journal of Human Genetics ·Katarina Lehmann, Petra Seemann, Fatma Sılan, Timm O. Goecke, (unknown), Klaus Kjaer, Søren K. Kjærgaard, M J Mahoney, Susanne Morlot, Carsten Reißner, Bronwyn Kerr, Andrew O.M. Wilkie, Stefan Mundlos	84
17	Sprachentwicklungsbehinderung beim Smith-Magenis-Syndrom 2006 ·HNO ·Christoph Bergmann, Susanne Morlot, M. Ptok	0
18	Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations 2006 ·Journal of Medical Genetics ·Martin Zenker, Katarina Lehmann, (unknown), Heidi Barth, (unknown), Rainer Koenig, Rudolf Korinthenberg, Martina Kreiß‐Nachtsheim, Peter Meinecke, Susanne Morlot, Stefan Mundlos, Anne S. Quante, Salmo Raskin, Dirk Schnabel, Lore Wehner, Christian P. Kratz, Denise Horn, Kerstin Kutsche	136
19	Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes 2004 ·American Journal of Obstetrics and Gynecology ·Albrecht Röpke, (unknown), Marianne Volleth, (unknown), Susanne Morlot, Peter Wieacker	18
20	Novel Mutations in the Gene Encoding Secreted Lymphocyte Antigen-6/Urokinase-type Plasminogen Activator Receptor-related Protein-1 (SLURP-1) and Description of Five Ancestral Haplotypes in Patients with Mal de Meleda 2003 ·Journal of Investigative Dermatology ·Slaheddine Marrakchi, (unknown), H. Turki, (unknown), B. Bouadjar, Cristina Has, Caroline Lefèvre, Colin S. Munro, Susan Cure, Florence Jobard, Susanne Morlot, Daniel Hohl, Jean-François Prud’homme, Judith Fischer	28

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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