Reinhard Ullmann

9.4k total citations
132 papers, 4.8k citations indexed

About

Reinhard Ullmann is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Reinhard Ullmann has authored 132 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Genetics, 68 papers in Molecular Biology and 22 papers in Plant Science. Recurrent topics in Reinhard Ullmann's work include Genomic variations and chromosomal abnormalities (59 papers), Genetics and Neurodevelopmental Disorders (24 papers) and Chromosomal and Genetic Variations (20 papers). Reinhard Ullmann is often cited by papers focused on Genomic variations and chromosomal abnormalities (59 papers), Genetics and Neurodevelopmental Disorders (24 papers) and Chromosomal and Genetic Variations (20 papers). Reinhard Ullmann collaborates with scholars based in Germany, Denmark and United States. Reinhard Ullmann's co-authors include D.M. Kolb, T. Will, Hans‐Hilger Ropers, Fikret Erdogan, Wei Chen, Andreas Tzschach, Vera M. Kalscheuer, Niels Tommerup, Eva Klopocki and Helmut Popper and has published in prestigious journals such as Science, Nature Genetics and The Journal of Experimental Medicine.

In The Last Decade

Reinhard Ullmann

129 papers receiving 4.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Reinhard Ullmann Germany	38	2.3k	2.2k	433	398	349	132	4.8k
Marc Lalande United States	40	4.6k 2.0×	3.6k 1.6×	1.1k 2.5×	445 1.1×	401 1.1×	83	6.6k
Michael R. James Australia	41	2.3k 1.0×	1.3k 0.6×	72 0.2×	126 0.3×	1.1k 3.1×	106	5.7k
Eric T. Ahrens United States	41	1.4k 0.6×	625 0.3×	80 0.2×	214 0.5×	448 1.3×	94	6.5k
James Ellis Canada	44	5.1k 2.2×	1.9k 0.9×	170 0.4×	204 0.5×	334 1.0×	123	7.1k
Naoyuki Fujita Japan	29	2.6k 1.1×	732 0.3×	77 0.2×	124 0.3×	409 1.2×	98	3.7k
Saul Surrey United States	37	2.5k 1.1×	662 0.3×	417 1.0×	164 0.4×	196 0.6×	162	5.8k
Mark Mercola United States	59	8.0k 3.5×	1.2k 0.6×	141 0.3×	245 0.6×	496 1.4×	166	10.4k
David F. Albertini United States	50	4.1k 1.8×	1.2k 0.5×	1.3k 2.9×	305 0.8×	129 0.4×	177	9.4k
Ali H. Brivanlou United States	53	11.8k 5.1×	1.2k 0.5×	330 0.8×	233 0.6×	1.3k 3.7×	117	15.2k
Tohru Yamamoto Japan	41	2.9k 1.3×	554 0.2×	45 0.1×	136 0.3×	355 1.0×	198	6.0k

Countries citing papers authored by Reinhard Ullmann

Since Specialization

Citations

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

Fields of papers citing papers by Reinhard Ullmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reinhard Ullmann

This figure shows the co-authorship network connecting the top 25 collaborators of Reinhard Ullmann. A scholar is included among the top collaborators of Reinhard Ullmann 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 Reinhard Ullmann. Reinhard Ullmann 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:

20 of 20 papers shown

Ullmann, Reinhard, et al.. (2020). A Versatile Lambda-Dynamics Module for GROMACS. Biophysical Journal. 118(3). 138a–138a. 1 indexed citations

Becker, Benjamin V., Chalid Assaf, Markus Möbs, et al.. (2018). Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line. Frontiers in Oncology. 8. 183–183. 7 indexed citations

Ullmann, Reinhard, Carsten Kutzner, A. Beckmann, et al.. (2017). A Flexible, GPU - Powered Fast Multipole Method for Realistic Biomolecular Simulations in Gromacs. Biophysical Journal. 112(3). 448a–448a. 6 indexed citations

Haider, Ahmed, Reinhard Ullmann, Michael Hummel, et al.. (2016). Inactivation of RUNX3/p46 Promotes Cutaneous T-Cell Lymphoma. Journal of Investigative Dermatology. 136(11). 2287–2296. 13 indexed citations

Weißmann, Robert, Allan Lind-Thomsen, Matthias Peiser, et al.. (2014). Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. BMC Genomics. 15(1). 537–537. 5 indexed citations

Huppke, Peter, Cornelia Brendel, Vera M. Kalscheuer, et al.. (2012). Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin. The American Journal of Human Genetics. 90(1). 61–68. 68 indexed citations

Ullmann, Reinhard & G. Matthias Ullmann. (2012). GMCT : A Monte Carlo simulation package for macromolecular receptors. Journal of Computational Chemistry. 33(8). 887–900. 36 indexed citations

Derivery, Emmanuel, Hongbo Hu, Masoud Garshasbi, et al.. (2011). Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP. Human Molecular Genetics. 20(13). 2585–2590. 62 indexed citations

Fullston, Tod, David F. Callen, Reinhard Ullmann, et al.. (2011). Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 204–214. 15 indexed citations

10.

Thorwarth, Anne, Heike Biebermann, Hans‐Hilger Ropers, et al.. (2010). Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis. The Journal of Clinical Endocrinology & Metabolism. 95(7). 3446–3452. 22 indexed citations

11.

Kahrizi, Kimia, Masoud Garshasbi, Seyedeh Sedigheh Abedini, et al.. (2010). Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. European Journal of Human Genetics. 19(1). 115–117. 49 indexed citations

12.

Kariminejad, Ariana, Roxana Kariminejad, Andreas Tzschach, et al.. (2010). 11q14.1‐11q22.1 deletion in a 1‐year‐old male with minor dysmorphic features. American Journal of Medical Genetics Part A. 152A(10). 2651–2655. 4 indexed citations

13.

Storlazzi, Clelia Tiziana, Angelo Lonoce, Maria Corsignano Guastadisegni, et al.. (2010). Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure. Genome Research. 20(9). 1198–1206. 168 indexed citations

14.

Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations

15.

Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations

16.

Motazacker, Mohammad Mahdi, Benjamin R. Rost, Tim Hucho, et al.. (2007). A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 81(4). 792–798. 112 indexed citations

17.

Mefford, Heather C., Séverine Clauin, Andrew J. Sharp, et al.. (2007). Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy. The American Journal of Human Genetics. 81(5). 1057–1069. 185 indexed citations

18.

Meyer, Stefan, William Fergusson, Anthony D. Whetton, et al.. (2007). Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes Chromosomes and Cancer. 46(4). 359–372. 24 indexed citations

19.

Schwarzbraun, Thomas, Reinhard Ullmann, Christian Windpassinger, et al.. (2006). Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetic and Genome Research. 115(1). 84–89. 6 indexed citations

20.

Erdogan, Fikret, Reinhard Ullmann, Wei Chen, et al.. (2006). Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay. American Journal of Medical Genetics Part A. 143A(2). 172–178. 46 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.

Explore authors with similar magnitude of impact