E.I. Schwartz

931 citations

40 papers · 665 · h-index 16

Impact in

Clinical Biochemistry top 5%
- Paraoxonase enzyme and polymorphisms
- Metabolism and Genetic Disorders
Endocrinology, Diabetes and Metabolism top 10%
- Diabetes Management and Research
- Hormonal Regulation and Hypertension

Papers in

Molecular Biology 15
Genetics 11
- Diabetes and associated disorders 3
- Nutrition, Genetics, and Disease 3

Co-authors: L S Taitz (2 shared papers)Sergey V. Anisimov (3 shared papers)Jorma Ilonen (3 shared papers)Alexei A. Goltsov (4 shared papers)Helena Reijonen (2 shared papers)Hans K. Åkerblom (2 shared papers)Sergei Nejentsev (2 shared papers)Svetlana Baranovskaya (3 shared papers)
Journals: Molecular Genetics and Metabolism (5 papers)Human Mutation (4 papers)Nucleic Acids Research (3 papers)PEDIATRICS (2 papers)Human Heredity (2 papers)
Partner nations: Russia United States Finland

In The Last Decade

E.I. Schwartz

40 papers receiving 635 citations

Peers

Countries citing papers authored by E.I. Schwartz

Since Specialization

Citations

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

Fields of papers citing papers by E.I. Schwartz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside E.I. Schwartz, 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.I. Schwartz Line = papers co-authored together E.I. Schwartz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Paraoxonase 1 Met–Leu 54 polymorphism is associated with Parkinson’s disease Journal of the Neurological Sciences ·S N Akhmedova, Andrey K Yakimovsky, E.I. Schwartz	2001	74
2	The Effect of HLA-B Allele on the IDDM Risk Defined by DRB104 Subtypes and DQB10302 Diabetes ·Sergei Nejentsev, Helena Reijonen, Bela Adojaan, L. Kovalchuk, Arthur Sochnevs, E.I. Schwartz, Hans K. Åkerblom, Jorma Ilonen	1997	57
3	Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans. PubMed ·Randy C. Eisensmith, Alexei A. Goltsov, C. O’Neill, Linda Tyfield, E.I. Schwartz, Alexei I. Kuzmin, Svetlana Baranovskaya, G L Tsukerman, Eileen P. Treacy, C. R. Scriver	1995	45
4	CONGENITAL ABSENCE OF THE PARATHYROID AND THYMUS GLANDS IN AN INFANT PEDIATRICS ·L S Taitz, Concepcion Zarate-Salvador, E.I. Schwartz	1966	40
5	Congenital absence of the parathyroid and thymus glands in an infant. (3 and 4 pharyngeal pouch syndrome). PubMed ·L S Taitz, Concepcion Zarate-Salvador, E.I. Schwartz	1966	38
6	Distribution of insulin‐dependent diabetes mellitus (IDDM)‐related HLA alleles correlates with the difference in IDDM incidence in four populations of the Eastern Baltic region Tissue Antigens ·Sergei Nejentsev, Suvi Koskinen, Minna Sjöroos, Helena Reijonen, E.I. Schwartz, L. Kovalchuk, A. Sochnev, Bela Adojaan, Toomas Podar, Mikael Knip, Olli Simell, M. Koskenvuo, Hans K. Åkerblom, Jorma Ilonen	1998	30
7	Approach to identification of a point mutation in apo B100 gene by means of a PCR-mediated site-directed mutagenesis Nucleic Acids Research ·E.I. Schwartz, Sergei Shevtsov, A.P. Kuchinski, Yu.P. Kovalev, O. V. Plutalov, Yu.A. Berlin	1991	30
8	Albuterol Protects Against Exercise-Induced Asthma Longer Than Metaproterenol Sulfate PEDIATRICS ·Robert Berkowitz, E.I. Schwartz, Don A. Bukstein, Michael Grunstein, Hyman Chai	1986	30
9	Methylenetetrahydrofolate Reductase Gene Polymorphism as a Risk Factor for Diabetic Nephropathy in IDDM Patients Molecular Genetics and Metabolism ·Н. С. Щербак, Zhanna V. Shutskaya, A.M. Sheidina, В. И. Ларионова, E.I. Schwartz	1999	26
10	Gln → Arg 191 Polymorphism of Paraoxonase and Parkinson’s Disease Human Heredity ·S N Akhmedova, Sergey V. Anisimov, Andrey K Yakimovsky, E.I. Schwartz	1999	25
11	Megakaryocyte-specific positive regulatory sequence 5' to the human PF4 gene. PubMed ·B Ramachandran, S Surrey, E.I. Schwartz	1995	20
12	Age-Associated Accumulation of the Apolipoprotein C-III Gene T-455C Polymorphism C Allele in a Russian Population The Journals of Gerontology Series A ·Sergey V. Anisimov, Mariya Volkova, L. V. Lenskaya, Khavinson VKh, D. V. Solovieva, E.I. Schwartz	2001	19
13	Gene–Gene Interaction in the RAS System in the Predisposition to Myocardial Infarction in Elder Population of St. Petersburg (Russia) Molecular Genetics and Metabolism ·Ekaterina Fomicheva, Svetlana P. Gukova, Valentina I. Larionova-Vasina, Yuri R. Kovalev, E.I. Schwartz	2000	18
14	Age as a Risk Factor for Myocardial Infarction in Leiden Mutation Carriers Molecular Genetics and Metabolism ·Svetlana Baranovskaya, Sergey Kudinov, Ekaterina Fomicheva, Valentina Vasina, Dina V. Solovieva, Khavinson VKh, E.I. Schwartz	1998	17
15	Cushing's syndrome in pregnancy International Journal of Gynecology & Obstetrics ·Hamida Khakoo, E.I. Schwartz, V.T. Pillari, Ralph E. Peterson	1982	16
16	Frequency of a Specific Cytochrome P4502D6B (CYP2D6B) Mutant Allele in Clinically Differentiated Groups of Patients with Parkinson Disease Biochemical and Molecular Medicine ·S N Akhmedova, Elena A. Pushnova, Andrei F. Yakimovsky, V V Avtonomov, E.I. Schwartz	1995	15
17	A novel frameshift mutation causing β-thalassaemia in Azerbaijan Nucleic Acids Research ·E.I. Schwartz, Alexei A. Goltsov, O. K. Kaboev, Andrei Alexeev, G. Ya. Solovyev, В. Л. Сурин, А В Лукьяненко, Sergei V. Vinogradov, Yu. A. Berlin	1989	15
18	The spectrum of β-thalassemia mutations in Azerbaijan Human Mutation ·A. F. Tagiev, В. Л. Сурин, Alexei A. Goltsov, А В Лукьяненко, G. Ya. Solovyev, E. A. Gulieva, O. V. Plutalov, O. K. Kaboev, Т А Мамедова, T. S. Dadasheva, Rafail Rustamov, E.I. Schwartz, Yu. A. Berlin	1993	14
19	Comparative Analysis of Apo(A) Gene Alleles: Distribution of Pentanucleotide Repeats in Position −1373 and C/T Transition in Position +93 among Patients with Myocardial Infarction and a Control Group in St. Petersburg, Russia Biochemical and Molecular Medicine ·Maria Volkova, Valentina Vasina, Ekaterina Fomicheva, E.I. Schwartz	1997	12
20	The frequency of cytochrome P450 2C9 genetic variants in the Russian population and their associations with individual sensitivity to warfarin therapy Thrombosis Research ·Sofya Pchelina, О. В. Сироткина, А. Е. Тараскина, Т. В. Вавилова, Alexander L. Shwarzman, E.I. Schwartz	2004	12

About E.I. Schwartz

E.I. Schwartz is a scholar working on Molecular Biology, Genetics, Surgery, Clinical Biochemistry and Cardiology and Cardiovascular Medicine, having authored 40 papers that have together received 665 indexed citations. Recurring topics across this work include Pharmacogenetics and Drug Metabolism (5 papers), Metabolism and Genetic Disorders (4 papers), Lipoproteins and Cardiovascular Health (4 papers), Cancer, Lipids, and Metabolism (3 papers), Diabetes and associated disorders (3 papers), Folate and B Vitamins Research (3 papers), Nutrition, Genetics, and Disease (3 papers) and Cancer Treatment and Pharmacology (2 papers). The work is most often cited by research in Clinical Biochemistry (129 citations), Endocrinology, Diabetes and Metabolism (120 citations), Aging (12 citations), Hematology (74 citations) and Genetics (164 citations). E.I. Schwartz has collaborated with scholars based in Russia, United States and Finland. Frequent co-authors include L S Taitz, Sergey V. Anisimov, Jorma Ilonen, Alexei A. Goltsov, Helena Reijonen, Hans K. Åkerblom, Sergei Nejentsev, Svetlana Baranovskaya, Sergei Shevtsov and Robert Berkowitz. Their work appears in journals such as Molecular Genetics and Metabolism, Human Mutation, Nucleic Acids Research, PEDIATRICS and Human Heredity.

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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E.I. Schwartz

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