Donald W. Day

551 total citations
17 papers, 349 citations indexed

About

Donald W. Day is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Donald W. Day has authored 17 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Donald W. Day's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and RNA modifications and cancer (3 papers). Donald W. Day is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and RNA modifications and cancer (3 papers). Donald W. Day collaborates with scholars based in United States, France and Mexico. Donald W. Day's co-authors include Mary K. Kukolich, Robert J. Gorlin, Natalie Krassikoff, Charles Jennings, Renata Laxová, Leonard O. Langer, Lowell D. Lutter, Golder N. Wilson, S. M. Jalal and Diane S. Roe and has published in prestigious journals such as Genomics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

Donald W. Day

17 papers receiving 341 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Donald W. Day United States	12	227	179	65	50	31	17	349
Lawrence G. Leichtman United States	11	173 0.8×	129 0.7×	66 1.0×	10 0.2×	31 1.0×	14	379
Marie‐Pierre Cordier France	11	189 0.8×	168 0.9×	119 1.8×	13 0.3×	59 1.9×	34	438
Alina Khromykh United States	10	164 0.7×	202 1.1×	36 0.6×	41 0.8×	26 0.8×	13	367
Jean‐Marie Rival France	12	186 0.8×	191 1.1×	72 1.1×	12 0.2×	36 1.2×	24	370
Friedel Wenzel Switzerland	11	164 0.7×	136 0.8×	145 2.2×	9 0.2×	26 0.8×	21	341
Julie Scuffins United States	5	215 0.9×	123 0.7×	126 1.9×	16 0.3×	37 1.2×	10	348
F. R. Sergovich Canada	13	348 1.5×	232 1.3×	172 2.6×	10 0.2×	20 0.6×	20	548
Alison Lashwood United Kingdom	10	168 0.7×	141 0.8×	268 4.1×	24 0.5×	34 1.1×	20	439
Ko–ichiro Yoshiura Japan	12	251 1.1×	304 1.7×	107 1.6×	9 0.2×	31 1.0×	22	505
Rina Schmidt United States	12	257 1.1×	164 0.9×	109 1.7×	6 0.1×	32 1.0×	20	430

Countries citing papers authored by Donald W. Day

Since Specialization

Citations

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

Fields of papers citing papers by Donald W. Day

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Donald W. Day. 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 Donald W. Day. The network helps show where Donald W. Day may publish in the future.

Co-authorship network of co-authors of Donald W. Day

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

All Works

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17 of 17 papers shown

Day, Donald W.. (2013). Circular Error Probability (CEP) of in a De-Reefed Parachute Payload Recovery System in Stratospheric Flights. 1 indexed citations

Garcia‐Heras, Jaime, et al.. (1999). De novo partial duplications 1p: Report of two new cases and review. American Journal of Medical Genetics. 82(3). 261–264. 23 indexed citations

Yang, Bing-Zhi, Jia-Huan Ding, Diane S. Roe, et al.. (1998). Identification of Four Novel Mutations in Patients with Carnitine Palmitoyltransferase II (CPT II) Deficiency. Molecular Genetics and Metabolism. 64(4). 229–236. 25 indexed citations

Yang, Bing-Zhi, et al.. (1998). A Novel Mutation Identified in Carnitine Palmitoyltransferase II Deficiency. Molecular Genetics and Metabolism. 63(2). 110–115. 26 indexed citations

Garcia‐Heras, Jaime, Judith A. Martin, Donald W. Day, Peter C. Scacheri, & Selma F. Witchel. (1997). “De novo” duplication Xq23→Xq26 of paternal origin in a girl with a mildly affected phenotype. American Journal of Medical Genetics. 70(4). 404–408. 13 indexed citations

Kulharya, Anita S., Mark C. Maberry, Mary K. Kukolich, et al.. (1995). Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Rieger anomaly. American Journal of Medical Genetics. 55(2). 165–170. 28 indexed citations

Lewanda, Amy Feldman, M. Michael Cohen, Charles E. Jackson, et al.. (1994). Genetic Heterogeneity among Craniosynostosis Syndromes: Mapping the Saethre-Chotzen Syndrome Locus between D7S513 and D7S516 and Exclusion of Jackson-Weiss and Crouzon Syndrome Loci from 7p. Genomics. 19(1). 115–119. 26 indexed citations

Day, Donald W., et al.. (1992). Clasped‐thumb mental retardation (MASA) syndrome: Confirmation of linkage to Xq28. American Journal of Medical Genetics. 43(1-2). 408–414. 21 indexed citations

Jabs, Ethylin Wang, Cathleen A. Coss, S. J. Hayflick, et al.. (1991). Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region. Genomics. 11(1). 188–192. 28 indexed citations

10.

Jalal, S. M., et al.. (1991). Tetrasomy 9p: an emerging syndrome. Clinical Genetics. 39(1). 60–64. 19 indexed citations

11.

Jalal, S. M., et al.. (1989). Familial transmission of 16p trisomy in an infant. Human Genetics. 81(2). 196–198. 20 indexed citations

12.

Day, Donald W., et al.. (1988). Direct chromosome analysis from neonatal cord blood. American Journal of Medical Genetics. 31(4). 943–946. 5 indexed citations

13.

Langer, Leonard O., Natalie Krassikoff, Renata Laxová, et al.. (1984). The tricho‐rhino‐phalangeal syndrome with exostoses (or Langer‐Giedion syndrome): Four additional patients without mental retardation and review of the literature. American Journal of Medical Genetics. 19(1). 81–112. 78 indexed citations

14.

Day, Donald W.. (1984). Genetics of Congenital Lip Defects. Clinics in Plastic Surgery. 11(4). 693–700. 6 indexed citations

15.

Day, Donald W.. (1981). Perspectives on Care: The Interdisciplinary Team Approach. Otolaryngologic Clinics of North America. 14(4). 769–775. 8 indexed citations

16.

Day, Donald W.. (1981). Perspectives on care: the interdisciplinary team approach.. PubMed. 14(4). 769–75. 8 indexed citations

17.

Motohashi, Nobuyoshi, Samuel Pruzansky, & Donald W. Day. (1981). Roentgencephalometric analysis of craniofacial growth in the Johanson-Blizzard syndrome.. PubMed. 1(1). 57–72. 14 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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