E Małunowicz

1.5k citations

31 papers · 953 indexed · h-index 14

Impact in

Endocrinology, Diabetes and Metabolism top 2%
- Hormonal Regulation and Hypertension
- Hormonal and reproductive studies
- Adrenal Hormones and Disorders
Pharmacology top 5%
- Pharmacogenetics and Drug Metabolism

Papers in ⓘ

Endocrinology, Diabetes and Metabolism 21
- Hormonal and reproductive studies 13
- Hormonal Regulation and Hypertension 9
- Adrenal Hormones and Disorders 9
- Growth Hormone and Insulin-like Growth Factors 3
Clinical Biochemistry 5
- Metabolism and Genetic Disorders 5

Co-authors: Cedric Shackleton (9 shared papers)Wiebke Arlt (8 shared papers)Paul M. Stewart (3 shared papers)Nicole L. Draper (2 shared papers)S. Chalder (2 shared papers)Jon P. Ride (2 shared papers)Berthold P. Hauffa (2 shared papers)Fabian Hammer (1 shared paper)
Journals: The Journal of Clinical Endocrinology & Metabolism (4 papers)Journal of Inherited Metabolic Disease (2 papers)Nature Genetics (1 paper)Endocrinology (1 paper)Molecular Genetics and Metabolism (1 paper)
Partner nations: Poland United Kingdom Germany

In The Last Decade

E Małunowicz

29 papers receiving 926 citations

Peers

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-authors

The 25 scholars most cited alongside E Małunowicz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E Małunowicz Line = papers co-authored together E Małunowicz links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study The Lancet ·Wiebke Arlt, Elizabeth A. Walker, Nicole L. Draper, Hannah E Ivison, Jon P. Ride, Fabian Hammer, S. Chalder, Maria Borucka-Mankiewicz, Berthold P. Hauffa, E Małunowicz, Paul M. Stewart, Cedric Shackleton	2004	236
2	Mutations in the genes encoding 11β-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency Nature Genetics ·Nicole L. Draper, Elizabeth A. Walker, Iwona Bujalska, Jeremy Tomlinson, S. Chalder, Wiebke Arlt, Gareth G. Lavery, Oliver Bedendo, David Ray, Ian Laing, E Małunowicz, Perrin C. White, Martin Hewison, Philip J. Mason, John Connell, Cedric Shackleton, Paul M. Stewart	2003	228
3	The Diagnosis of Congenital Adrenal Hyperplasia in the Newborn by Gas Chromatography/Mass Spectrometry Analysis of Random Urine Specimens The Journal of Clinical Endocrinology & Metabolism ·Michael P. Caulfield, Thomas C. Lynn, Michael Gottschalk, Kenneth L. Jones, Norman Taylor, E Małunowicz, Cedric Shackleton, Richard E. Reitz, Delbert A. Fisher	2002	91
4	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 ·Gareth G. Lavery, Elizabeth A. Walker, Ana Tiganescu, Jon P. Ride, Cedric Shackleton, Jeremy Tomlinson, John Connell, David Ray, Anna Biason‐Lauber, E Małunowicz, Wiebke Arlt, Paul M. Stewart	2008	60
5	Biochemical diagnosis of Antley–Bixler syndrome by steroid analysis American Journal of Medical Genetics Part A ·Cedric Shackleton, Josep Marcos, E Małunowicz, Maria Szarras‐Czapnik, Petr Jira, Norman Taylor, Nuala Murphy, Ellen Crushell, Michael Gottschalk, Berthold P. Hauffa, Deborah Cragun, Robert J. Hopkin, Masanori Adachi, Wiebke Arlt	2004	58
6	Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency The Journal of Clinical Endocrinology & Metabolism ·Jan Idkowiak, Stephen O’Riordan, Nicole Reisch, E Małunowicz, Felicity Collins, Michiel N. Kerstens, Birgit Köhler, Luitgard Graul‐Neumann, Maria Szarras‐Czapnik, Mehul Dattani, Martin Silink, Cedric Shackleton, Dominique Maiter, Nils Krone, Wiebke Arlt	2010	34
7	Congenital adrenal hyperplasia due to 21-hydroxylase deficiency - management in adults. PubMed ·Urszula Ambroziak, Tomasz Bednarczuk, Maria Ginalska-Malinowska, E Małunowicz, Barbara Grzechocińska, Paweł Kamiński, L Bablok, J Przedlacki, Ewa Bar‐Andziak	2010	28
8	The diagnosis of nonclassic congenital adrenal hyperplasia due to 21‐hydroxylase deficiency, based on serum basal or post‐ACTH stimulation 17‐hydroxyprogesterone, can lead to false‐positive diagnosis Clinical Endocrinology ·Urszula Ambroziak, Anna Kępczyńska‐Nyk, Alina Kuryłowicz, E Małunowicz, Anna Wójcicka, Piotr Miśkiewicz, Magdalena Macech	2015	26
9	DHCR7 mutations and genotype–phenotype correlation in 37 Polish patients with Smith–Lemli–Opitz syndrome Clinical Genetics ·Elżbieta Ciara, MJM Nowaczyk, Martina Witsch‐Baumgartner, E Małunowicz, Ewa Popowska, Aleksandra Jezela‐Stanek, Małgorzata Piotrowicz, JS Waye, Gerd Utermann, Małgorzata Krajewska‐Walasek	2004	22
10	11β-Hydroxysteroid Dehydrogenase Type 1 Deficiency (‘Apparent Cortisone Reductase Deficiency’) in a 6-Year-Old Boy Hormone Research in Paediatrics ·E Małunowicz, T E Romer, Maria D. Urban, Artur Bossowski	2003	20
11	Concomitant Mutations in the P450 Oxidoreductase and Androgen Receptor Genes Presenting with 46,XY Disordered Sex Development and Androgenization at Adrenarche The Journal of Clinical Endocrinology & Metabolism ·Jan Idkowiak, E Małunowicz, Vivek Dhir, Nicole Reisch, Maria Szarras‐Czapnik, Donna M. Holmes, Cedric Shackleton, John Dwyfor Davies, Ieuan A. Hughes, Nils Krone, Wiebke Arlt	2010	18
12	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 ·Nguyễn Huy Hoàng, Antje Eiden-Plach, Frank Hannemann, E Małunowicz, Michaela F. Hartmann, Stefan A. Wudy, Rita Bernhardt	2015	16
13	Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analyses Molecular Genetics and Metabolism ·Nguyễn Huy Hoàng, Frank Hannemann, Michaela F. Hartmann, E Małunowicz, Stefan A. Wudy, Rita Bernhardt	2010	15
14	Mild Smith-Lemli-Opitz syndrome: Further delineation of 5 Polish cases and review of the literature European Journal of Medical Genetics ·Aleksandra Jezela‐Stanek, Elżbieta Ciara, E Małunowicz, L Korniszewski, Dorota Piekutowska‐Abramczuk, Ewa Popowska, Małgorzata Krajewska‐Walasek	2007	14
15	Differences between predicted and established diagnoses of Smith‐Lemli‐Opitz syndrome in the Polish population: underdiagnosis or loss of affected fetuses? Journal of Inherited Metabolic Disease ·Aleksandra Jezela‐Stanek, Elżbieta Ciara, E Małunowicz, Krystyńa Chrzańowska, Anna Latos‐Bieleńska, Małgorzata Krajewska‐Walasek, (unknown)	2010	13
16	Sepiapterin reductase deficiency in a 2‐year‐old girl with incomplete response to treatment during short‐term follow‐up Journal of Inherited Metabolic Disease ·Katarzyna Kuśmierska, Erwin E. W. Jansen, C. Jakobs, Krystyna Szymańska, E Małunowicz, D. Meilei, Beat Thöny, Nenad Blau, Jolanta Tryfon, Dariusz Rokicki, Ewa Pronicka, Jolanta Sykut‐Cegielska	2009	12
17	LC-MS/MS improves screening towards 21-hydroxylase deficiency Gynecological Endocrinology ·Urszula Ambroziak, Anna Kępczyńska‐Nyk, Alina Kuryłowicz, Aleksandra Wysłouch‐Cieszyńska, E Małunowicz, Zbigniew Bartoszewicz, Agnieszka Kondracka, Radosław Jaźwiec, Emilia Pawłowska, Magdalena Szcześniak, Michał Dadlez, Tomasz Bednarczuk	2014	9
18	Combined deficiency of 17 alpha-hydroxylase and 21-hydroxylase in an 8 years old girl. PubMed ·E Małunowicz, Romer Te, Maria Szarras‐Czapnik, Zbigniew Mielniczuk, Danuta Gajewska	1987	9
19	Hydrogen transfer reactions catalysed by cobalt complexes I. Hydrogen transfer between cyclohexanone and isopropyl alcohol catalyzed by a derivative of tris(triphenylphosphine)cobalt trihydride Journal of Organometallic Chemistry ·E Małunowicz, S. Tyrlik, Z. Łasocki	1974	9
20	Assessment of adrenocortical function in asthmatic patients on long-term triamcinolone acetonide treatment. PubMed ·W Droszcz, E Małunowicz, B Lech, H Krawczyńska, M Madalińska	1979	8

About E Małunowicz

E Małunowicz is a scholar working on Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Molecular Biology, Behavioral Neuroscience and Obstetrics and Gynecology, having authored 31 papers that have together received 953 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (14 papers), Hormonal and reproductive studies (13 papers), Hormonal Regulation and Hypertension (9 papers), Adrenal Hormones and Disorders (9 papers), Metabolism and Genetic Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Cholesterol and Lipid Metabolism (3 papers) and Growth Hormone and Insulin-like Growth Factors (3 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (588 citations), Pharmacology (138 citations), Clinical Biochemistry (107 citations), Behavioral Neuroscience (33 citations) and Reproductive Medicine (78 citations). E Małunowicz has collaborated with scholars based in Poland, United Kingdom and Germany. Frequent co-authors include Cedric Shackleton, Wiebke Arlt, Paul M. Stewart, Nicole L. Draper, S. Chalder, Jon P. Ride, Berthold P. Hauffa, Fabian Hammer, Hannah E Ivison and Elizabeth A. Walker. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Inherited Metabolic Disease, Nature Genetics, Endocrinology and Molecular Genetics and Metabolism.

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