E Małunowicz

1.5k total citations
31 papers, 953 citations indexed

About

E Małunowicz is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, E Małunowicz has authored 31 papers receiving a total of 953 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Endocrinology, Diabetes and Metabolism, 20 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in E Małunowicz's work include Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (13 papers) and Adrenal Hormones and Disorders (9 papers). E Małunowicz is often cited by papers focused on Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (13 papers) and Adrenal Hormones and Disorders (9 papers). E Małunowicz collaborates with scholars based in Poland, United Kingdom and Germany. E Małunowicz's co-authors include Cedric Shackleton, Wiebke Arlt, Paul M. Stewart, S. Chalder, Nicole L. Draper, Jon P. Ride, Berthold P. Hauffa, Elizabeth A. Walker, Hannah E Ivison and Fabian Hammer and has published in prestigious journals such as The Lancet, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

E Małunowicz

29 papers receiving 926 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E Małunowicz Poland 14 588 547 237 138 120 31 953
Masaaki Kagimoto United States 13 392 0.7× 566 1.0× 228 1.0× 328 2.4× 36 0.3× 24 963
Jeffrey D. Kearbey United States 12 475 0.8× 307 0.6× 260 1.1× 57 0.4× 28 0.2× 16 895
Jacob G. Ghazarian United States 14 388 0.7× 227 0.4× 166 0.7× 162 1.2× 30 0.3× 36 1.0k
Gundula Grimberg Germany 9 139 0.2× 142 0.3× 41 0.2× 63 0.5× 130 1.1× 9 630
Eiji Kutoh Japan 15 273 0.5× 426 0.8× 118 0.5× 20 0.1× 128 1.1× 51 762
O. Sonne Denmark 14 158 0.3× 473 0.9× 53 0.2× 19 0.1× 203 1.7× 25 847
H D Chern United States 9 46 0.1× 343 0.6× 251 1.1× 144 1.0× 42 0.3× 12 694
Karen A. Veverka United States 12 154 0.3× 241 0.4× 116 0.5× 30 0.2× 22 0.2× 35 610
Ralph Cash United States 5 85 0.1× 81 0.1× 122 0.5× 43 0.3× 29 0.2× 7 339
Alan C. Gough United Kingdom 11 23 0.0× 333 0.6× 117 0.5× 316 2.3× 12 0.1× 12 645

Countries citing papers authored by E Małunowicz

Since Specialization
Citations

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

Fields of papers citing papers by E Małunowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Małunowicz

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

All Works

20 of 20 papers shown
1.
Rojek, Aleksandra, M Krawczyński, Aleksander Jamsheer, et al.. (2016). X-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the EntireNR0B1 (DAX1)andMAGEB1–4Genes. International Journal of Endocrinology. 2016. 1–7. 4 indexed citations
2.
Hoàng, Nguyễn Huy, Frank Hannemann, E Małunowicz, et al.. (2015). Phenotypic, metabolic, and molecular genetic characterization of six patients with congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene. The Journal of Steroid Biochemistry and Molecular Biology. 155(Pt A). 126–134. 16 indexed citations
3.
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Ambroziak, Urszula, Alina Kuryłowicz, Aleksandra Wysłouch‐Cieszyńska, et al.. (2014). LC-MS/MS improves screening towards 21-hydroxylase deficiency. Gynecological Endocrinology. 31(4). 296–300. 9 indexed citations
6.
Idkowiak, Jan, Vivek Dhir, Angela M. Taylor, et al.. (2012). Broad phenotypic spectrum of 17[alpha]-hydroxylase deficiency: Functional characterisation of 4 novel mutations in the CYP17A1 gene. 1 indexed citations
7.
Januś, Dominika, Małgorzata Wójcik, E Małunowicz, & Jerzy Starzyk. (2012). A case of recurrent labial adhesions in a 15-month-old child with asymptomatic non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Journal of Pediatric Endocrinology and Metabolism. 25(9-10). 1017–21. 5 indexed citations
8.
Hoàng, Nguyễn Huy, Frank Hannemann, Michaela F. Hartmann, et al.. (2010). Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analyses. Molecular Genetics and Metabolism. 100(4). 357–364. 15 indexed citations
9.
Idkowiak, Jan, Stephen O’Riordan, Nicole Reisch, et al.. (2010). Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 96(3). E453–E462. 34 indexed citations
10.
Lavery, Gareth G., Elizabeth A. Walker, Ana Tiganescu, et al.. (2008). Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 93(10). 3827–3832. 60 indexed citations
11.
Jezela‐Stanek, Aleksandra, Elżbieta Ciara, E Małunowicz, et al.. (2007). Mild Smith-Lemli-Opitz syndrome: Further delineation of 5 Polish cases and review of the literature. European Journal of Medical Genetics. 51(2). 124–140. 14 indexed citations
12.
Shackleton, Cedric, Josep Marcos, E Małunowicz, et al.. (2004). Biochemical diagnosis of Antley–Bixler syndrome by steroid analysis. American Journal of Medical Genetics Part A. 128A(3). 223–231. 58 indexed citations
13.
Ciara, Elżbieta, Martina Witsch‐Baumgartner, E Małunowicz, et al.. (2004). DHCR7 mutations and genotype–phenotype correlation in 37 Polish patients with Smith–Lemli–Opitz syndrome. Clinical Genetics. 66(6). 517–524. 22 indexed citations
14.
Arlt, Wiebke, Elizabeth A. Walker, Nicole L. Draper, et al.. (2004). Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study. The Lancet. 363(9427). 2128–2135. 236 indexed citations
15.
Małunowicz, E, T E Romer, Maria D. Urban, & Artur Bossowski. (2003). 11β-Hydroxysteroid Dehydrogenase Type 1 Deficiency (‘Apparent Cortisone Reductase Deficiency’) in a 6-Year-Old Boy. Hormone Research in Paediatrics. 59(4). 205–210. 20 indexed citations
16.
Draper, Nicole L., Elizabeth A. Walker, Iwona Bujalska, et al.. (2003). Mutations in the genes encoding 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency. Nature Genetics. 34(4). 434–439. 228 indexed citations
17.
Małunowicz, E, Maria Ginalska-Malinowska, T E Romer, & Karol Bal. (1998). The influence of prenatal dexamethasone treatment on urinary excretion of adrenocortical steroids in newborns. European Journal of Pediatrics. 157(7). 539–543. 6 indexed citations
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Małunowicz, E, et al.. (1987). Combined deficiency of 17 alpha-hydroxylase and 21-hydroxylase in an 8 years old girl.. PubMed. 38(1). 117–24. 9 indexed citations
20.
Małunowicz, E, et al.. (1980). Factors influencing adrenocortical suppression during long-term triamcinolone acetonide therapy in asthma.. PubMed. 44(3). 174–6. 4 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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