D R Romain

639 total citations
23 papers, 406 citations indexed

About

D R Romain is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, D R Romain has authored 23 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Plant Science and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in D R Romain's work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (9 papers). D R Romain is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (9 papers). D R Romain collaborates with scholars based in New Zealand, Australia and Switzerland. D R Romain's co-authors include R H Smythe, C J Chapman, Alan McDermott, David F. Callen, Elizabeth Baker, Helen J. Eyre, Eric Haan, Joanne Dixon, Jay P. Goldsmith and James R. Seip and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

D R Romain

22 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D R Romain New Zealand	12	371	186	162	143	21	23	406
Roberto Coco Argentina	12	401 1.1×	156 0.8×	213 1.3×	143 1.0×	24 1.1×	45	531
Michelle Macha United States	8	435 1.2×	183 1.0×	228 1.4×	181 1.3×	18 0.9×	8	503
Lorraine Gaunt United Kingdom	10	249 0.7×	108 0.6×	146 0.9×	50 0.3×	17 0.8×	16	368
L. Wiśniewski Poland	11	305 0.8×	115 0.6×	134 0.8×	129 0.9×	17 0.8×	28	390
Sue Ann Berend United States	15	432 1.2×	336 1.8×	174 1.1×	149 1.0×	39 1.9×	20	584
Joleen L. Zackowski United States	11	311 0.8×	107 0.6×	151 0.9×	105 0.7×	16 0.8×	13	379
Elisabeth Ewers Germany	13	381 1.0×	175 0.9×	162 1.0×	222 1.6×	11 0.5×	23	423
B Quack France	13	396 1.1×	128 0.7×	250 1.5×	195 1.4×	17 0.8×	23	513
N. Morichon-Delvallez France	12	320 0.9×	143 0.8×	173 1.1×	74 0.5×	66 3.1×	26	418
Morag N. Collinson United Kingdom	14	381 1.0×	123 0.7×	210 1.3×	97 0.7×	25 1.2×	21	473

Countries citing papers authored by D R Romain

Since Specialization

Citations

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

Fields of papers citing papers by D R Romain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D R Romain. 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 D R Romain. The network helps show where D R Romain may publish in the future.

Co-authorship network of co-authors of D R Romain

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

All Works

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20 of 20 papers shown

Robinson, Wendy P., Fosco Bernasconi, Fabrizio Dutly, et al.. (1996). Molecular studies of translocations and trisomy involving chromosome 13. American Journal of Medical Genetics. 61(2). 158–163. 35 indexed citations

Romain, D R, et al.. (1994). Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35).. Journal of Medical Genetics. 31(8). 652–653. 19 indexed citations

Fitzgerald, P. H., et al.. (1994). Mosaicism with a normal cell line and an autosomal structural rearrangement.. Journal of Medical Genetics. 31(2). 108–114. 31 indexed citations

Romain, D R, et al.. (1994). Partial trisomy for2qina patient withdir dup(2) (q33. lq35).

Woodage, Trevor, Madhuri Prasad, Joanne Dixon, et al.. (1994). Bloom syndrome and maternal uniparental disomy for chromosome 15.. PubMed. 55(1). 74–80. 47 indexed citations

Romain, D R, et al.. (1992). Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p).. PubMed. 29(7). 513–513. 5 indexed citations

Romain, D R, et al.. (1991). A rare heteromorphism of chromosome 20 and reproductive loss.. Journal of Medical Genetics. 28(7). 477–478. 3 indexed citations

Romain, D R, et al.. (1990). Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).. Journal of Medical Genetics. 27(9). 588–589. 32 indexed citations

Romain, D R, et al.. (1990). Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7.. Journal of Medical Genetics. 27(2). 109–113. 26 indexed citations

10.

Romain, D R, et al.. (1989). Familial distal trisomy 8(q24.13----qter).. Journal of Medical Genetics. 26(2). 133–138. 12 indexed citations

11.

Romain, D R, et al.. (1988). Late replication studies and esterase D levels in a case of unbalanced X;autosome translocation, 46,X,t(X;13)(q27;q12).. Journal of Medical Genetics. 25(10). 716–718. 1 indexed citations

12.

Romain, D R, et al.. (1987). Partial monosomy 12p13.1----13.3.. Journal of Medical Genetics. 24(7). 434–436. 12 indexed citations

13.

Romain, D R, et al.. (1986). Studies on three rare fragile sites. Human Genetics. 73(2). 164–170. 3 indexed citations

14.

Romain, D R, et al.. (1985). A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf‐Hirschhorn syndrome. Clinical Genetics. 28(2). 166–172. 15 indexed citations

15.

Romain, D R, et al.. (1983). Two cases of ring chromosome 11.. Journal of Medical Genetics. 20(5). 380–382. 15 indexed citations

16.

Romain, D R, et al.. (1982). Cd branding studies in a homologous Robertsonian 13;13 translocation.. Journal of Medical Genetics. 19(4). 306–310. 4 indexed citations

17.

Romain, D R, et al.. (1982). Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems. Journal of Medical Genetics. 19(2). 153–155. 9 indexed citations

18.

Romain, D R. (1980). Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture. Pathology. 12(1). 136–136. 4 indexed citations

19.

McDermott, Alan, D R Romain, Iain D. C. Fraser, & G. L. Scott. (1978). Isochromosome 17q in two cases of acute blast transformation in myeloproliferative disorders. Human Genetics. 45(2). 215–218. 9 indexed citations

20.

McDermott, Alan, et al.. (1977). Ring chromosome 4.. Journal of Medical Genetics. 14(3). 228–232. 35 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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