W Voss

836 total citations
17 papers, 577 citations indexed

About

W Voss is a scholar working on Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Neurology. According to data from OpenAlex, W Voss has authored 17 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 7 papers in Pulmonary and Respiratory Medicine and 4 papers in Neurology. Recurrent topics in W Voss's work include Infant Development and Preterm Care (7 papers), Neonatal Respiratory Health Research (6 papers) and Neonatal and fetal brain pathology (4 papers). W Voss is often cited by papers focused on Infant Development and Preterm Care (7 papers), Neonatal Respiratory Health Research (6 papers) and Neonatal and fetal brain pathology (4 papers). W Voss collaborates with scholars based in Germany, Finland and United Kingdom. W Voss's co-authors include E Kattner, Tanja Jungmann, Y. Nivoche, Norma B. Romero, Arnaud Lemainque, Carsten G. Bönnemann, Michel Fardeau, Ana Ferreiro, Pascale Guicheney and Heinz Jungbluth and has published in prestigious journals such as Annals of Neurology, Pediatric Research and Acta Paediatrica.

In The Last Decade

W Voss

17 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
W Voss Germany	8	296	180	166	81	79	17	577
Cheryl E. Hanna United States	16	265 0.9×	183 1.0×	212 1.3×	56 0.7×	24 0.3×	27	845
Flavia Napoli Italy	19	156 0.5×	224 1.2×	347 2.1×	46 0.6×	67 0.8×	58	997
Edward S. Emery United States	12	232 0.8×	152 0.8×	43 0.3×	24 0.3×	85 1.1×	18	532
Anne Marie Childs United Kingdom	9	68 0.2×	39 0.2×	225 1.4×	36 0.4×	49 0.6×	14	456
Werner F. Blum Germany	16	213 0.7×	59 0.3×	299 1.8×	95 1.2×	13 0.2×	20	1.1k
Susanna Moskau Germany	14	124 0.4×	92 0.5×	138 0.8×	87 1.1×	51 0.6×	23	610
Niels Jacob Aachmann‐Andersen Denmark	13	36 0.1×	44 0.2×	102 0.6×	68 0.8×	37 0.5×	19	554
Ayako Hattori Japan	15	69 0.2×	40 0.2×	203 1.2×	52 0.6×	27 0.3×	60	546
H Schedewie United States	14	86 0.3×	39 0.2×	122 0.7×	23 0.3×	17 0.2×	32	532
Todd A. Briscoe Australia	11	222 0.8×	65 0.4×	82 0.5×	47 0.6×	8 0.1×	16	395

Countries citing papers authored by W Voss

Since Specialization

Citations

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

Fields of papers citing papers by W Voss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W Voss

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

17 of 17 papers shown

Voss, W, et al.. (2016). The Development of Extremely Premature Infants. Deutsches Ärzteblatt international. 113(51-52). 871–878. 16 indexed citations

Petermann, Franz, et al.. (2015). Qualitätsanalysen zur Entwicklung Frühgeborener: Ergebnisse des Niedersächsischen Frühgeborenen-Nachuntersuchungsprojekts und eines Vergleichskollektivs reif geborener Kinder. Zeitschrift für Evidenz Fortbildung und Qualität im Gesundheitswesen. 109(1). 6–17. 2 indexed citations

Voss, W, et al.. (2012). Long‐term cognitive outcomes of extremely low‐birth‐weight infants: the influence of the maternal educational background. Acta Paediatrica. 101(6). 569–573. 70 indexed citations

Harms, Karsten, et al.. (2011). Landesweite Nachuntersuchung extrem unreifer Frühgeborener: Ein Modell sektorübergreifender Qualitätsanalyse. Zeitschrift für Evidenz Fortbildung und Qualität im Gesundheitswesen. 105(8). 597–605. 4 indexed citations

Voss, W, et al.. (2010). Erythropoietin improves neurodevelopmental outcome of extremely preterm infants. Annals of Neurology. 67(5). 657–666. 84 indexed citations

Schara, Ulrike, H.‐J. Christen, Hacer Durmuş, et al.. (2009). Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. European Journal of Paediatric Neurology. 14(4). 326–333. 40 indexed citations

Heinen, Florian, Leonhard Döderlein, W Voss, et al.. (2009). Grafikgestützter Konsensus für die Behandlung von Bewegungsstörungen bei Kindern mit bilateralen spastischen Zerebralparesen (BS-CP). Monatsschrift Kinderheilkunde. 157(8). 789–794. 6 indexed citations

Voss, W, et al.. (2009). Intrathekale Baclofentherapie. Monatsschrift Kinderheilkunde. 157(11). 1128–1136. 4 indexed citations

Schara, Ulrike, Marja Hietala, Carmelo Rodolico, et al.. (2007). G.P.10.01 Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Neuromuscular Disorders. 17(9-10). 818–818. 2 indexed citations

10.

Voss, W, et al.. (2007). Neurodevelopmental outcome in extremely low birth weight infants: what is the minimum age for reliable developmental prognosis?. Acta Paediatrica. 96(3). 342–347. 50 indexed citations

11.

Voss, W, et al.. (2007). Outcome of extremely low birth weight survivors at school age: the influence of perinatal parameters on neurodevelopment. European Journal of Pediatrics. 167(1). 87–95. 114 indexed citations

12.

Schmidt, Carolin, Angela Abicht, K Krampfl, et al.. (2003). Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase. Neuromuscular Disorders. 13(3). 245–251. 41 indexed citations

13.

Ferreiro, Ana, Nicole Monnier, Norma B. Romero, et al.. (2002). A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene. Annals of Neurology. 51(6). 750–759. 137 indexed citations

14.

Krammer, Barbara, et al.. (1994). [Spontaneous, massive liver hemorrhage as a complication of thrombolysis with ultra-high dose streptokinase in deep thrombophlebitis].. PubMed. 23(4). 373–6. 4 indexed citations

15.

Hoffmann, G. F., P. G. Barth, W. Lehnert, et al.. (1991). 134 PROGRESSIVE ATAXIA AND MENTAL RETARDATION ASSOCIATED WITH LEUCODYSTROPHY IN 4 PATIENTS WITH L-2-HYDROXY-GLUTARIC ACIDURIA. Pediatric Research. 30(6). 650–650. 1 indexed citations

16.

Brämswig, Jürgen, G. Schellong, & W Voss. (1979). [Concordant leukemia in identical twins (author's transl)].. PubMed. 191(2). 140–4. 1 indexed citations

17.

Voss, W. (1953). [Contribution to air sickness prevention].. PubMed. 26. 879–81. 1 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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