Regine Schubert

937 citations

23 papers · 550 indexed · h-index 13

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Reproductive Medicine top 5%
- Sperm and Testicular Function

Papers in

Genetics 19
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Genetic Syndromes and Imprinting 2
Reproductive Medicine 4
- Sperm and Testicular Function 4

Co-authors: Gesa Schwanitz Thomas Eggermann H. van der Ven Markus Montag Katrin van der Ven Hartmut Engels M. Hansmann Roland Kruse
Journals: Clinical Genetics (4 papers)Prenatal Diagnosis (3 papers)Fertility and Sterility (1 paper)Human Reproduction (1 paper)The Journal of Urology (1 paper)
Partner nations: Germany Poland Hungary

In The Last Decade

Regine Schubert

22 papers receiving 493 citations

Peers

Countries citing papers authored by Regine Schubert

Since Specialization

Citations

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

Fields of papers citing papers by Regine Schubert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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

20 of 20 papers shown

#	Work
1	Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself Clinical Genetics ·HC Prematilaka, Matthias Begemann, Lukas Soellner, Dieter Meschede, Tsyrul'nikov Lg, Miriam Elbracht, Regine Schubert, Thomas Eggermann	2016	44
2	Rare interstitial deletion 9q31.2 to q33.1 de novo: Longitudinal study in a patient over a period of more than 20 years American Journal of Medical Genetics Part A ·Ulrike Gamerdinger, Thomas Eggermann, Regine Schubert, Gesa Schwanitz, Martina Kreiß‐Nachtsheim	2008	10
3	Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees American Journal of Medical Genetics Part A ·Hartmut Engels, Thomas Eggermann, Almuth Caliebe, B. Pfannebecker, Regine Schubert, Herdit M. Schüler, Barbara Panasiuk, Jacek Zaremba, Anna Latos‐Bieleńska, Lucjusz Jakubowski, Klaus Zerres, Gesa Schwanitz, Alina T. Midro	2008	45
4	Chromosomal aberrations in 130 patients with multiple myeloma studied by interphase FISH: diagnostic and prognostic relevance Cancer Genetics and Cytogenetics ·Ingo Schmidt‐Wolf, Axel Glasmacher, Corinna Hahn‐Ast, David Carbó Ochoa, Theresia M. Schnurr, F. W. Cremer, Thomas Moehler, Hartmut Goldschmidt, 吕鸿声, Regine Schubert, Gesa Schwanitz	2006	19
5	Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15. PubMed ·Chang Sun, Gesa Schwanitz, Regine Schubert, Karlijn van der Ven, Markus Montag	2006	15
6	Ring Chromosome 18: Clinical, Cytogenetic and Molecular Genetic Studies on Four Patients International Journal of Human Genetics ·Cao Sheng, György Fekete, Ramesh Bhonde, Regine Schubert, Judit Szabó, Zita Halász, T Fahad Affan, Thomas Eggermann, Gesa Schwanitz	2004	4
7	Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: Clinical report and review of the literature American Journal of Medical Genetics ·Regine Schubert, Thomas Eggermann, C. Hofstaetter, Елена Борисовна Гоголевская, G Knöpfle, Gesa Schwanitz	2002	16
8	Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases Clinical Genetics ·Katja Eggermann, Fereshteh Farhi, D J Rowlanda, Erika Koltai, Hartmut Engels, Regine Schubert, Thomas Eggermann, Ramesh Bhonde, Gesa Schwanitz	2002	56
9	Combination of Hypospadias and Maldescended Testis as Cardinal Symptoms in Gonosomal Chromosome Aberrations* European Journal of Pediatric Surgery ·Ramesh Bhonde, Regine Schubert, Gesa Schwanitz, 美幸永野, P Brühl	2000	6
10	On the Accuracy of a New Displacement Instrumentation for Rotary Tablet Presses Drug Development and Industrial Pharmacy ·Renata Marques Godoy e Silva Coutrin, Annette Bauer‐Brandl, W. V. Struve, Regine Schubert, Shinya Tsukamoto	1999	23
11	Characterisation, phenotypic manifestations and X‐inactivation pattern in 14 patients with X‐autosome translocations Clinical Genetics ·Alison Baker-Lewton, Angela L.S. Fernandez, Gesa Schwanitz, Regine Schubert	1999	42
12	Analysis of ade novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescencein situ hybridization and spectral karyotyping Prenatal Diagnosis ·Enrique Mart�nez, Ayush Chirutkar, B Shibu, M. Hansmann, Evelin Schröck, Thomas Ried, Hartmut Engels, Gesa Schwanitz, Regine Schubert	1999	18
13	Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature. PubMed ·Thomas Eggermann, Regine Schubert, Hartmut Engels, Can Apacik, S. Stengel‐Rutkowski, Carolina Haefliger, 刘森林, Yogesh Nagargoje, Gesa Schwanitz	1999	12
14	Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping Prenatal Diagnosis ·Enrique Mart�nez, LI Ze-ka, Volker Mertens, M. Hansmann, Evelin Schröck, Thomas Ried, Hartmut Engels, Gesa Schwanitz, Regine Schubert	1999	0
15	Maldescensus testis und Hypospadie bei Aberration der Geschlechtschromosomen Klinische Pädiatrie ·Ramesh Bhonde, Regine Schubert, Gesa Schwanitz, Katrin van der Ven, Hans‐Udo Schweikert, P Brühl	1998	3
16	Genetic Counseling in a Patient with XXY/XXXY/XY Mosaic Klinefelter’s Syndrome: Estimate of Sex Chromosome Aberrations in Sperm Before Intracytoplasmic Sperm Injection Fertility and Sterility ·Roland Kruse, Martina Guttenbach, A. E. Akulov, Regine Schubert, H. van der Ven, Michael Schmid, Peter Propping	1998	52
17	Genetic Counseling in a Patient With XXY/XXXY/XY Mosaic Klinefelter's Syndrome: Estimate of Sex Chromosome Aberrations in Sperm Before Intracytoplasmic Sperm Injection The Journal of Urology ·Roland Kruse, Martina Guttenbach, A. E. Akulov, Regine Schubert, H. van der Ven, Michael Schmid, Peter Propping	1998	5
18	Partial trisomy 6p from a de novo translocation (6; 18) with variable mosaicism in different tissues Clinical Genetics ·Shivam Wadhwa, Regine Schubert, Frank Majewski, Fritz Haverkamp, Gesa Schwanitz	1997	11
19	Report of two new cases of Pallister-Killian syndrome confirmed by FISH: Tissue-specific mosaicism and loss of i(12p) by in vitro selection American Journal of Medical Genetics ·Regine Schubert, Eszter Szlávich, Thomas Eggermann, M. Hansmann, Gesa Schwanitz	1997	38
20	MOLECULAR-CYTOGENETIC INVESTIGATIONS OF TEN TERM PLACENTAE IN CASES OF PRENATALLY DIAGNOSED MOSAICISM Prenatal Diagnosis ·Regine Schubert, Ramesh Bhonde, Gesa Schwanitz	1996	2

About Regine Schubert

Regine Schubert is a scholar working on Genetics, Reproductive Medicine, Urology, Plant Science and Pediatrics, Perinatology and Child Health, having authored 23 papers that have together received 550 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Sexual Differentiation and Disorders (5 papers), Prenatal Screening and Diagnostics (5 papers), Sperm and Testicular Function (4 papers), Genomics and Chromatin Dynamics (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (429 citations), Reproductive Medicine (108 citations), Pediatrics, Perinatology and Child Health (232 citations), Plant Science (137 citations) and Pharmaceutical Science (21 citations). Regine Schubert has collaborated with scholars based in Germany, Poland and Hungary. Frequent co-authors include Gesa Schwanitz, Thomas Eggermann, H. van der Ven, Markus Montag, Katrin van der Ven, Hartmut Engels, M. Hansmann, Roland Kruse, Michael Schmid and Peter Propping. Their work appears in journals such as Clinical Genetics, Prenatal Diagnosis, Fertility and Sterility, Human Reproduction and The Journal of Urology.

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