G. Gemelos

1.1k total citations
10 papers, 702 citations indexed

About

G. Gemelos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, G. Gemelos has authored 10 papers receiving a total of 702 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 9 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in G. Gemelos's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Syndromes and Imprinting (2 papers). G. Gemelos is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Syndromes and Imprinting (2 papers). G. Gemelos collaborates with scholars based in United States. G. Gemelos's co-authors include Matthew Rabinowitz, Allison Ryan, Milena Banjevic, Johan Banér, Matthew D. Hill, Cengiz Cinnioğlu, Zachary Demko, David S. Johnson, Robert M. Ross and Styrmir Sigurjonsson and has published in prestigious journals such as PLoS ONE, Human Reproduction and Fertility and Sterility.

In The Last Decade

G. Gemelos

10 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Gemelos United States	5	633	300	185	148	113	10	702
L. Spizzichino Italy	8	652 1.0×	394 1.3×	216 1.2×	166 1.1×	49 0.4×	12	759
R. Prates United States	7	536 0.8×	321 1.1×	181 1.0×	148 1.0×	35 0.3×	13	615
Francesca Malvestiti Italy	13	590 0.9×	343 1.1×	61 0.3×	98 0.7×	160 1.4×	19	660
Norio Miharu Japan	15	459 0.7×	292 1.0×	168 0.9×	159 1.1×	146 1.3×	27	717
Beatrice Grimi Italy	12	626 1.0×	389 1.3×	69 0.4×	108 0.7×	155 1.4×	17	695
G. Heleen Schuring‐Blom Netherlands	10	360 0.6×	175 0.6×	75 0.4×	74 0.5×	85 0.8×	16	413
Melody White United States	11	574 0.9×	299 1.0×	178 1.0×	92 0.6×	53 0.5×	15	646
J. Fischer United States	9	714 1.1×	315 1.1×	320 1.7×	145 1.0×	47 0.4×	18	829
Cristina Agrati Italy	8	415 0.7×	231 0.8×	42 0.2×	116 0.8×	108 1.0×	11	497

Countries citing papers authored by G. Gemelos

Since Specialization

Citations

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

Fields of papers citing papers by G. Gemelos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Gemelos

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

All Works

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10 of 10 papers shown

Lathi, Ruth B., Megan Loring, Zachary Demko, et al.. (2012). Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics. PLoS ONE. 7(3). e31282–e31282. 35 indexed citations

Zimmermann, Bernhard, Matthew D. Hill, G. Gemelos, et al.. (2012). Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci. Prenatal Diagnosis. 32(13). 1233–1241. 235 indexed citations

Rabinowitz, Matthew, G. Gemelos, Matthew D. Hill, et al.. (2012). Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y. Fertility and Sterility. 98(3). S28–S29. 1 indexed citations

Lathi, Ruth B., Megan Loring, Zachary Demko, et al.. (2012). Correction: Informatics Enhanced SNP Microarray Analysis of 30 Miscarriage Samples Compared to Routine Cytogenetics. PLoS ONE. 7(8). 4 indexed citations

Rabinowitz, Matthew, Allison Ryan, G. Gemelos, et al.. (2011). Origins and rates of aneuploidy in human blastomeres. Fertility and Sterility. 97(2). 395–401. 105 indexed citations

Rabinowitz, Matthew, et al.. (2011). First Clinical Outcomes Reported on Patients Undergoing PGD for Genetic Disorders Together With 24 Chromosome Ploidy Using Microarrays. Fertility and Sterility. 95(4). S6–S7. 2 indexed citations

Rabinowitz, Matthew, B. Pettersen, Anh Le, G. Gemelos, & David E Tourgeman. (2011). DNA Fingerprinting Confirmation of Healthy Livebirth Following PGS Results: Indicating Trisomy 3 of Paternal Origin and Likely Embryo Mosaicism. Fertility and Sterility. 95(4). S11–S11. 2 indexed citations

Rabinowitz, Matthew, D. Potter, Zachary Demko, G. Gemelos, & Jutta Keller. (2011). Concordance Between Day 3 and Day 5 Biopsy Results: Using 24-Chromosome Aneuploidy Screening Method. Fertility and Sterility. 95(4). S11–S12. 1 indexed citations

Johnson, David S., G. Gemelos, Johan Banér, et al.. (2010). Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol. Human Reproduction. 25(4). 1066–1075. 178 indexed citations

10.

Johnson, David S., Cengiz Cinnioğlu, Robert M. Ross, et al.. (2010). Comprehensive analysis of karyotypic mosaicism between trophectoderm and inner cell mass. Molecular Human Reproduction. 16(12). 944–949. 139 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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