H.‐D. Rott

869 total citations
40 papers, 639 citations indexed

About

H.‐D. Rott is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, H.‐D. Rott has authored 40 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in H.‐D. Rott's work include Genomic variations and chromosomal abnormalities (6 papers), Tuberous Sclerosis Complex Research (4 papers) and Neonatal Respiratory Health Research (4 papers). H.‐D. Rott is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Tuberous Sclerosis Complex Research (4 papers) and Neonatal Respiratory Health Research (4 papers). H.‐D. Rott collaborates with scholars based in Germany, Netherlands and Estonia. H.‐D. Rott's co-authors include R. A. Pfeiffer, Raimund Fahsold, Gesa Schwanitz, Gabriele E. Lang, Peter Lorenz, Thomas Liehr, Udo Trautmann, Anita Rauch, Holger Hoehn and J Lejeune and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and The Pediatric Infectious Disease Journal.

In The Last Decade

H.‐D. Rott

39 papers receiving 588 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H.‐D. Rott Germany	13	342	212	127	118	88	40	639
K. Fried Israel	16	301 0.9×	337 1.6×	149 1.2×	57 0.5×	54 0.6×	64	844
Diana García‐Cruz Mexico	16	356 1.0×	272 1.3×	112 0.9×	55 0.5×	37 0.4×	81	727
J G Lesko United States	12	274 0.8×	383 1.8×	308 2.4×	42 0.4×	63 0.7×	15	805
Nicholas C. Bethlenfalvay United States	10	155 0.5×	153 0.7×	88 0.7×	31 0.3×	53 0.6×	28	451
J. Zonana United States	16	416 1.2×	484 2.3×	96 0.8×	28 0.2×	34 0.4×	29	767
Richard C. Juberg United States	16	335 1.0×	157 0.7×	198 1.6×	82 0.7×	26 0.3×	45	617
A Rinaldi Italy	12	191 0.6×	215 1.0×	128 1.0×	47 0.4×	25 0.3×	35	476
Atsuko Fujimoto United States	19	489 1.4×	310 1.5×	267 2.1×	153 1.3×	11 0.1×	45	868
R. A. Pfeiffer Germany	14	405 1.2×	293 1.4×	120 0.9×	69 0.6×	35 0.4×	39	714
B. Rafael Elejalde United States	15	467 1.4×	357 1.7×	230 1.8×	33 0.3×	22 0.3×	39	833

Countries citing papers authored by H.‐D. Rott

Since Specialization

Citations

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

Fields of papers citing papers by H.‐D. Rott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.‐D. Rott. 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 H.‐D. Rott. The network helps show where H.‐D. Rott may publish in the future.

Co-authorship network of co-authors of H.‐D. Rott

This figure shows the co-authorship network connecting the top 25 collaborators of H.‐D. Rott. A scholar is included among the top collaborators of H.‐D. Rott 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 H.‐D. Rott. H.‐D. Rott 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

Rott, H.‐D.. (2008). Lungenhämorrhagien durch diagnostischen Ultraschall. Ultraschall in der Medizin - European Journal of Ultrasound. 18(5). 226–228. 1 indexed citations

Rott, H.‐D.. (2008). Diagnostischer Ultraschall: Biologische Wirkungen und potentielle Risiken*. Ultraschall in der Medizin - European Journal of Ultrasound. 9(1). 2–4.

Rott, H.‐D.. (1998). Discussion. European Journal of Ultrasound. 8(1). 67–68. 7 indexed citations

König, Carl Heinz Wirsing von, H.‐D. Rott, H. Bogaerts, & H Schmitt. (1998). A serologic study of organisms possibly associated with pertussis-like coughing. The Pediatric Infectious Disease Journal. 17(7). 645–649. 35 indexed citations

Rauch, Anita, et al.. (1992). A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH). Clinical Genetics. 42(2). 84–90. 74 indexed citations

Rott, H.‐D. & Raimund Fahsold. (1991). Tuberous sclerosis in two sibs of normal parents. Clinical Genetics. 39(4). 306–308. 8 indexed citations

Fahsold, Raimund, H.‐D. Rott, & Peter Lorenz. (1991). A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus. Human Genetics. 88(1). 85–90. 41 indexed citations

Fahsold, Raimund, et al.. (1991). Tuberous sclerosis in a child with de novo translocation t(3; 12) (p26.3; q23.3). Clinical Genetics. 40(4). 326–328. 9 indexed citations

Lang, Gabriele E., H.‐D. Rott, & R. A. Pfeiffer. (1990). X-linked ocular albinism. Ophthalmic Paediatrics and Genetics. 11(4). 265–271. 35 indexed citations

10.

Rott, H.‐D., et al.. (1988). Ocular hypotelorism, submucosal cleft palate, and hypospadias: A new autosomal dominant syndrome. American Journal of Medical Genetics. 31(4). 863–870. 10 indexed citations

11.

Rott, H.‐D., et al.. (1987). [Analogy of Blaschko lines in the eye].. PubMed. 35(1). 19–27. 3 indexed citations

12.

Rott, H.‐D., et al.. (1985). Der Lyon-Effekt an der Linse: Konduktorinnenbefunde bei X-chromosomal gebundener Katarakt und beim Lowe-Syndrom. Klinische Monatsblätter für Augenheilkunde. 187(12). 525–528. 7 indexed citations

13.

Rott, H.‐D., et al.. (1984). Konduktorinnenstatus bei X-gebundenem, okulärem Albinismus: Ein Beleg für die Gültigkeit der Lyon-Hypothese beim Menschen. Klinische Monatsblätter für Augenheilkunde. 184(2). 128–129. 3 indexed citations

14.

Rott, H.‐D.. (1984). Duchenne muscular dystrophy: Carrier detection by ultrasonic imaging techniques. Ultrasonic Imaging. 6(2). 236–236. 2 indexed citations

15.

Rott, H.‐D.. (1984). Partial sweat gland aplasia in incontinentia pigmenti Bloch‐Sulzberger. Clinical Genetics. 26(1). 36–38. 10 indexed citations

16.

Mayer, U., Marco Klinger, & H.‐D. Rott. (1982). Über eine seltene Form von Opticus-, Choroidea- und Retina-Dysplasie in Kombination mit einer occipitalen Encephalocele. Graefe s Archive for Clinical and Experimental Ophthalmology. 219(2). 72–75. 8 indexed citations

17.

Rott, H.‐D., et al.. (1980). Der autosomal dominante, leichte Diabetes des Jugendalters (MODY)^1,2. Klinische Pädiatrie. 192(3). 229–234. 2 indexed citations

18.

Deshaies, Yves, et al.. (1979). [Recessive microencephaly linked to the X chromosome].. PubMed. 27(3). 221–36. 2 indexed citations

19.

Hornstein, O. P., H.‐D. Rott, Gesa Schwanitz, & G Grosse. (1974). Die XXYY-Variante des Klinefelter-Syndroms^*. DMW - Deutsche Medizinische Wochenschrift. 99(6). 248–251. 3 indexed citations

20.

Rott, H.‐D., et al.. (1972). Chromosomenbefunde bei Ehepaaren mit geh�uften Aborten. Archives of Gynecology and Obstetrics. 213(2). 110–118. 10 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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