Sandra C. Doelken

2.3k total citations
16 papers, 425 citations indexed

About

Sandra C. Doelken is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Sandra C. Doelken has authored 16 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Sandra C. Doelken's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Biomedical Text Mining and Ontologies (4 papers). Sandra C. Doelken is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Biomedical Text Mining and Ontologies (4 papers). Sandra C. Doelken collaborates with scholars based in Germany, United Kingdom and United States. Sandra C. Doelken's co-authors include Peter N. Robinson, Sebastian Köhler, Eva Klopocki, Stefan Mundlos, Damian Smedley, Chris Mungall, Ricarda Flöttmann, Malte Spielmann, R. Habenicht and Aleksander Jamsheer and has published in prestigious journals such as PLoS ONE, Genome Research and PLoS Genetics.

In The Last Decade

Sandra C. Doelken

16 papers receiving 409 citations

Peers

Sandra C. Doelken

GENET

Karl Heinz Grzeschik Germany

Alina Khromykh United States

Randi Koll Germany

Josef Davidsson Sweden

Sara Benito‐Sanz Spain

Denise E. Mauldin United States

Ursula Kobalz Germany

M E Oude Luttikhuis United Kingdom

Angeline Lai Singapore

Prajnya Ranganath India

Karl Heinz Grzeschik Germany

Sandra C. Doelken

229 ×0.8

99 ×0.4

GENET

25 ×0.5

3 ×0.1

12 ×0.4

Citations per year, relative to Sandra C. Doelken Sandra C. Doelken (= 1×) peers Karl Heinz Grzeschik

Countries citing papers authored by Sandra C. Doelken

Since Specialization

Citations

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

Fields of papers citing papers by Sandra C. Doelken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra C. Doelken. 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 Sandra C. Doelken. The network helps show where Sandra C. Doelken may publish in the future.

Co-authorship network of co-authors of Sandra C. Doelken

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra C. Doelken. A scholar is included among the top collaborators of Sandra C. Doelken 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 Sandra C. Doelken. Sandra C. Doelken is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Groza, Tudor, Sebastian Köhler, Sandra C. Doelken, et al.. (2015). Automatic concept recognition using the Human Phenotype Ontology reference and test suite corpora. Database. 2015(0). bav005–bav005. 39 indexed citations

Lohan, Silke B., Malte Spielmann, Sandra C. Doelken, et al.. (2014). Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas‐type polysyndactyly and Laurin‐Sandrow syndrome. Clinical Genetics. 86(4). 318–325. 48 indexed citations

Köhler, Sebastian, Johanna Christina Czeschik, Sandra C. Doelken, et al.. (2014). Clinical interpretation of CNVs with cross-species phenotype data. Journal of Medical Genetics. 51(11). 766–772. 17 indexed citations

Tayebi, Naeimeh, Aleksander Jamsheer, Ricarda Flöttmann, et al.. (2014). 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. Orphanet Journal of Rare Diseases. 9(1). 108–108. 33 indexed citations

Zimmer, Julia, Maria Walther, Carsten Reißner, et al.. (2013). A GDF5 Point Mutation Strikes Twice - Causing BDA1 and SYNS2. PLoS Genetics. 9(10). e1003846–e1003846. 34 indexed citations

Ibrahim, Daniel M., Christian Rödelsperger, Asita C. Stiege, et al.. (2013). Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations. Genome Research. 23(12). 2091–2102. 24 indexed citations

Jamsheer, Aleksander, Tomasz Żemojtel, Mateusz Kolanczyk, et al.. (2013). Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. Journal of Medical Genetics. 50(9). 579–584. 25 indexed citations

Graul‐Neumann, Luitgard, Ulrike Wille, Naseebullah Kakar, et al.. (2013). Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe. European Journal of Human Genetics. 22(6). 726–733. 19 indexed citations

Köhler, Sebastian, Sandra C. Doelken, Ana Rath, Ségolène Aymé, & Peter N. Robinson. (2012). Ontological phenotype standards for neurogenetics. Human Mutation. 33(9). 1333–1339. 16 indexed citations

10.

Heidemann, Simone, Christine Fischer, Christoph Engel, et al.. (2012). Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management. Breast Cancer Research and Treatment. 134(3). 1229–1239. 43 indexed citations

11.

Zimmer, Julia, Sandra C. Doelken, Denise Horn, et al.. (2012). Functional Analysis of Alleged NOGGIN Mutation G92E Disproves Its Pathogenic Relevance. PLoS ONE. 7(4). e35062–e35062. 1 indexed citations

12.

Doelken, Sandra C., et al.. (2012). Proximal and distal 15q25.2 microdeletions–genotype–phenotype delineation of two neurodevelopmental susceptibility loci. American Journal of Medical Genetics Part A. 161(1). 218–224. 23 indexed citations

13.

Chen, Chao-Kung, Chris Mungall, Georgios V. Gkoutos, et al.. (2012). MouseFinder: Candidate disease genes from mouse phenotype data. Human Mutation. 33(5). 858–866. 38 indexed citations

14.

Doelken, Sandra C., Sebastian Köhler, Chris Mungall, et al.. (2012). Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish. Disease Models & Mechanisms. 6(2). 358–72. 30 indexed citations

15.

Guo, Gao, Petra Gehle, Sandra C. Doelken, et al.. (2011). Induction of Macrophage Chemotaxis by Aortic Extracts from Patients with Marfan Syndrome Is Related to Elastin Binding Protein. PLoS ONE. 6(5). e20138–e20138. 33 indexed citations

16.

Doelken, Sandra C., Sebastian Köhler, Sebastian Bauer, et al.. (2010). Neue Wege in der bioinformatischen Phänotypanalyse. Medizinische Genetik. 22(2). 221–228. 2 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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