Doris Müller

761 total citations
13 papers, 575 citations indexed

About

Doris Müller is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Doris Müller has authored 13 papers receiving a total of 575 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Doris Müller's work include Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Chromosomal and Genetic Variations (2 papers). Doris Müller is often cited by papers focused on Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Chromosomal and Genetic Variations (2 papers). Doris Müller collaborates with scholars based in Germany, Austria and United Kingdom. Doris Müller's co-authors include Helmut Holzer, Jörg Mansfeld, Katrin Daniel, Caren Norden, Jaroslav Icha, J T Harries, Igor A. Gak, Dilyana Kirova, Thomas Zerjatke and Ingmar Glauche and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Gut.

In The Last Decade

Doris Müller

13 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Doris Müller Germany	11	366	116	77	61	54	13	575
Janice Saxton United Kingdom	16	378 1.0×	61 0.5×	58 0.8×	36 0.6×	75 1.4×	25	590
Bharati Kakkad United States	13	466 1.3×	88 0.8×	89 1.2×	61 1.0×	22 0.4×	14	594
Jeanne M. Richardson United States	7	430 1.2×	99 0.9×	44 0.6×	91 1.5×	30 0.6×	11	630
Hironori Hanada Japan	16	558 1.5×	107 0.9×	59 0.8×	33 0.5×	18 0.3×	24	774
K. Akai Japan	13	377 1.0×	33 0.3×	51 0.7×	46 0.8×	28 0.5×	20	727
Douglas J. Franks Canada	15	473 1.3×	90 0.8×	52 0.7×	82 1.3×	35 0.6×	31	793
C. Earl Guthrow United States	6	379 1.0×	155 1.3×	42 0.5×	77 1.3×	21 0.4×	7	702
András Frankó Germany	16	452 1.2×	81 0.7×	44 0.6×	70 1.1×	106 2.0×	27	755
Jesse Bakke United States	11	383 1.0×	99 0.9×	52 0.7×	58 1.0×	73 1.4×	18	640
Kendra D. Martyn United States	9	555 1.5×	50 0.4×	85 1.1×	26 0.4×	36 0.7×	10	1.0k

Countries citing papers authored by Doris Müller

Since Specialization

Citations

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

Fields of papers citing papers by Doris Müller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Doris Müller

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

All Works

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13 of 13 papers shown

Daniel, Katrin, et al.. (2018). Conditional control of fluorescent protein degradation by an auxin-dependent nanobody. Nature Communications. 9(1). 3297–3297. 86 indexed citations

Zerjatke, Thomas, Igor A. Gak, Dilyana Kirova, et al.. (2017). Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification. Cell Reports. 19(9). 1953–1966. 96 indexed citations

Bernkopf, Marie, Gerald Webersinke, Chintan N. Koyani, et al.. (2014). Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability. Human Molecular Genetics. 23(15). 4015–4023. 29 indexed citations

Schmitz, Klaus J., Georgios C. Sotiropoulos, Hideo A. Baba, et al.. (2011). AKR1B10 expression is associated with less aggressive hepatocellular carcinoma: a clinicopathological study of 168 cases. Liver International. 31(6). 810–816. 47 indexed citations

Müller, Doris, Ursula Albrecht, Matthias Baumann, et al.. (2010). Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21). American Journal of Medical Genetics Part A. 152A(11). 2762–2767. 17 indexed citations

Großmann, Vera, Doris Müller, Wilfried Müller, et al.. (2009). “Essentially” pure trisomy 3q27 → qter: Further delineation of the partial trisomy 3q phenotype. American Journal of Medical Genetics Part A. 149A(11). 2522–2526. 18 indexed citations

Talmud, Philippa J., June K. Lloyd, Doris Müller, et al.. (1988). Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia.. Journal of Clinical Investigation. 82(5). 1803–1806. 54 indexed citations

Stead, R J, Doris Müller, Susan Matthews, Mark E. Hodson, & J C Batten. (1986). Effect of abnormal liver function on vitamin E status and supplementation in adults with cystic fibrosis.. Gut. 27(6). 714–718. 28 indexed citations

Hecking, E., et al.. (1982). A controlled study of supplementation with essential amino acids and α-keto acids in the conservative management of patients with chronic renal failure. Zeitschrift für Ernährungswissenschaft. 21(4). 299–311. 6 indexed citations

10.

Müller, Doris & Helmut Holzer. (1981). Regulation of fructose-1,6-bisphosphatase in yeast by phosphorylation/dephosphorylation. Biochemical and Biophysical Research Communications. 103(3). 926–933. 129 indexed citations

11.

Ogilvie, Donald, et al.. (1976). Urinary outputs of oxalate, calcium, and magnesium in children with intestinal disorders. Potential cause of renal calculi.. Archives of Disease in Childhood. 51(10). 790–795. 19 indexed citations

12.

Prellwitz, W., et al.. (1976). Vergleich von Methoden zur Aktivitätsbestimmung der Serumcholinesterasen (Acylcholin-acylhydrolase E. C. 3.1.1.8) und deren diagnostische Wertigkeit. Clinical Chemistry and Laboratory Medicine (CCLM). 14(1-12). 93–7. 6 indexed citations

13.

Müller, Doris, et al.. (1975). Proceedings: Studies on the mechanism of fat absorption in congenital isolated lipase deficiency.. PubMed. 16(10). 838–838. 40 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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