Miriam S. DiMaio

695 total citations
14 papers, 355 citations indexed

About

Miriam S. DiMaio is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Miriam S. DiMaio has authored 14 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 9 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Miriam S. DiMaio's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Miriam S. DiMaio is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Miriam S. DiMaio collaborates with scholars based in United States, Italy and Israel. Miriam S. DiMaio's co-authors include Maurice J. Mahoney, Julie S. Fryburg, Howard M. Saal, Robert M. Greenstein, Teresa L. Yang‐Feng, Alan E. Donnenfeld, M J Mahoney, Amy Cronister, Stephanie Hallam and Peining Li and has published in prestigious journals such as New England Journal of Medicine, American Journal of Obstetrics and Gynecology and American Journal of Kidney Diseases.

In The Last Decade

Miriam S. DiMaio

13 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Miriam S. DiMaio United States	9	229	211	101	52	34	14	355
Anne M. Bandholz United States	6	332 1.4×	355 1.7×	154 1.5×	70 1.3×	23 0.7×	8	515
B. Pettersen United States	8	254 1.1×	207 1.0×	77 0.8×	40 0.8×	51 1.5×	12	406
Nathalie Leporrier France	15	251 1.1×	167 0.8×	153 1.5×	94 1.8×	9 0.3×	24	478
Irene Mademont‐Soler Spain	16	220 1.0×	186 0.9×	224 2.2×	55 1.1×	10 0.3×	28	572
Sandra Peacock United States	9	207 0.9×	308 1.5×	183 1.8×	25 0.5×	20 0.6×	11	489
Violaine Kerbrat France	12	313 1.4×	115 0.5×	250 2.5×	55 1.1×	14 0.4×	27	547
Mary Ann Thomas Canada	10	126 0.6×	180 0.9×	123 1.2×	45 0.9×	9 0.3×	46	361
Angelique J. A. Kooper Netherlands	13	289 1.3×	178 0.8×	35 0.3×	46 0.9×	7 0.2×	20	359
MarkW. Steele United States	5	234 1.0×	122 0.6×	59 0.6×	117 2.3×	11 0.3×	7	361
Tung‐Yao Chang Taiwan	12	191 0.8×	171 0.8×	104 1.0×	109 2.1×	4 0.1×	35	357

Countries citing papers authored by Miriam S. DiMaio

Since Specialization

Citations

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

Fields of papers citing papers by Miriam S. DiMaio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Miriam S. DiMaio. 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 Miriam S. DiMaio. The network helps show where Miriam S. DiMaio may publish in the future.

Co-authorship network of co-authors of Miriam S. DiMaio

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

All Works

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14 of 14 papers shown

Murphy, Erin L., et al.. (2018). Preimplantation Genetic Diagnosis Counseling in Autosomal Dominant Polycystic Kidney Disease. American Journal of Kidney Diseases. 72(6). 866–872. 27 indexed citations

DiMaio, Miriam S., Hui Yang, Maurice J. Mahoney, James McGrath, & Peining Li. (2016). Familial GPC3 and GPC4-TFDP3 deletions at Xq26 associated with Simpson-Golabi-Behmel syndrome. Meta Gene. 11. 147–151. 3 indexed citations

Li, Peining, Miriam S. DiMaio, Michael R. Rossi, et al.. (2011). Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization. American Journal of Medical Genetics Part A. 155(7). 1605–1615. 28 indexed citations

DiMaio, Miriam S., Joyce E. Fox, & Maurice J. Mahoney. (2010). Prenatal Diagnosis: Cases & Clinical Challenges. 2 indexed citations

Fattal‐Valevski, Aviva, Miriam S. DiMaio, Fuki M. Hisama, et al.. (2009). Variable Expression of a Novel PLP1 Mutation in Members of a Family With Pelizaeus-Merzbacher Disease. Journal of Child Neurology. 24(5). 618–624. 8 indexed citations

Rossi, Michael R., Miriam S. DiMaio, Bixia Xiang, et al.. (2009). Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature. American Journal of Medical Genetics Part A. 149A(12). 2788–2794. 41 indexed citations

Cronister, Amy, Miriam S. DiMaio, Maurice J. Mahoney, Alan E. Donnenfeld, & Stephanie Hallam. (2005). Fragile X syndrome carrier screening in the prenatal genetic counseling setting. Genetics in Medicine. 7(4). 246–250. 44 indexed citations

Evans, Mark I., et al.. (2005). Automated microscopy of amniotic fluid cells for the detection of fish signals: A method to increase accuracy and lower costs. American Journal of Obstetrics and Gynecology. 193(6). S160–S160. 1 indexed citations

DiMaio, Miriam S., et al.. (2002). Réflexions autour de la prise en charge en maternité des ictères sévères. Archives de Pédiatrie. 9(10). 1083–1086.

10.

Fryburg, Julie S., Miriam S. DiMaio, Teresa L. Yang‐Feng, & Maurice J. Mahoney. (1993). Follow‐up of pregnancies complicated by placental mosaicism diagnosed by chorionic villus sampling. Prenatal Diagnosis. 13(6). 481–494. 49 indexed citations

11.

DiMaio, Miriam S., Richard A. Barth, Kathryn Koprivnikar, et al.. (1993). First‐trimester prenatal diagnosis of osteogenesis imperfecta type II by DNA analysis and sonography. Prenatal Diagnosis. 13(7). 589–596. 22 indexed citations

12.

Fryburg, Julie S., Miriam S. DiMaio, & M J Mahoney. (1992). Postnatal placental confirmation of trisomy 2 and trisomy 16 detected at chorionic villus sampling: A possible association with intrauterine growth retardation and elevated maternal serum alpha‐fetoprotein. Prenatal Diagnosis. 12(3). 157–162. 26 indexed citations

13.

Sciorra, Leonard J., et al.. (1992). Trisomy 5 mosaicism detected prenatally with an affected liveborn. Prenatal Diagnosis. 12(6). 477–482. 15 indexed citations

14.

DiMaio, Miriam S., et al.. (1987). Screening for Fetal Down's Syndrome in Pregnancy by Measuring Maternal Serum Alpha-Fetoprotein Levels. New England Journal of Medicine. 317(6). 342–346. 89 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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