Harold N. Bass

850 total citations
34 papers, 552 citations indexed

About

Harold N. Bass is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Harold N. Bass has authored 34 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Harold N. Bass's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Harold N. Bass is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Harold N. Bass collaborates with scholars based in United States. Harold N. Bass's co-authors include Barbara F. Crandall, Robert S. Sparkes, Benjamin Emanuel, Maria Casado, H. Mabel Preloran, Carole H. Browner, Ann P. Walker, S. Michael Marcy, R S Sparkes and Rebecca Mardach and has published in prestigious journals such as JAMA, PEDIATRICS and Social Science & Medicine.

In The Last Decade

Harold N. Bass

34 papers receiving 498 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Harold N. Bass United States	16	273	195	112	92	64	34	552
Theodore Kushnick United States	15	336 1.2×	174 0.9×	200 1.8×	53 0.6×	72 1.1×	40	573
R.R. Gordon United Kingdom	14	181 0.7×	109 0.6×	132 1.2×	30 0.3×	56 0.9×	42	558
Claudette Hajaj Gonzalez Brazil	15	196 0.7×	207 1.1×	193 1.7×	66 0.7×	172 2.7×	33	712
M L Martínez-Frías Spain	10	152 0.6×	103 0.5×	113 1.0×	45 0.5×	140 2.2×	20	459
M. L. Martínez‐Frías Spain	16	215 0.8×	148 0.8×	121 1.1×	48 0.5×	244 3.8×	31	549
Philip M. Marden United States	8	323 1.2×	196 1.0×	214 1.9×	45 0.5×	142 2.2×	12	710
Ichiro Matsui Japan	12	435 1.6×	108 0.6×	144 1.3×	78 0.8×	48 0.8×	21	727
Kamal K. Naguib Kuwait	14	269 1.0×	140 0.7×	189 1.7×	24 0.3×	95 1.5×	40	558
María Luisa Martínez‐Frías Spain	14	182 0.7×	151 0.8×	116 1.0×	34 0.4×	215 3.4×	61	593
Margaret Barrow United Kingdom	13	341 1.2×	231 1.2×	263 2.3×	43 0.5×	60 0.9×	18	738

Countries citing papers authored by Harold N. Bass

Since Specialization

Citations

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

Fields of papers citing papers by Harold N. Bass

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Harold N. Bass. 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 Harold N. Bass. The network helps show where Harold N. Bass may publish in the future.

Co-authorship network of co-authors of Harold N. Bass

This figure shows the co-authorship network connecting the top 25 collaborators of Harold N. Bass. A scholar is included among the top collaborators of Harold N. Bass 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 Harold N. Bass. Harold N. Bass 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

Aradhya, Swaroop, et al.. (2012). A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity. Genetics in Medicine. 15(1). 3–13. 16 indexed citations

Zhang, Shulin, Harold N. Bass, Amber N. Pursley, et al.. (2009). Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion. Molecular Genetics and Metabolism. 99(1). 53–57. 14 indexed citations

Liang, Shujian, et al.. (2008). A Pseudo-Full Mutation Identified in Fragile X Assay Reveals a Novel Base Change Abolishing an EcoRI Restriction Site. Journal of Molecular Diagnostics. 10(5). 469–474. 4 indexed citations

Browner, Carole H., H. Mabel Preloran, Maria Casado, Harold N. Bass, & Ann P. Walker. (2003). Genetic counseling gone awry: miscommunication between prenatal genetic service providers and Mexican-origin clients. Social Science & Medicine. 56(9). 1933–1946. 91 indexed citations

Bass, Harold N.. (2002). London Dysmorphology Database, London Neurogenetics Database & Dysmorphology Photo Library on CD-ROM. The American Journal of Human Genetics. 71(3). 687–687. 11 indexed citations

Bass, Harold N.. (2002). Full Text LINK - perinatal. The Permanente Journal. 6(1). 15–20. 6 indexed citations

Bass, Harold N., et al.. (1993). Michelin tire baby syndrome: Familial constriction bands during infancy and early childhood in four generations. American Journal of Medical Genetics. 45(3). 370–372. 16 indexed citations

Bass, Harold N., et al.. (1993). Association of generalized dystrophic epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha‐fetoprotein. Prenatal Diagnosis. 13(1). 55–59. 3 indexed citations

Herskowitz, Joel, et al.. (1991). Churg-Strauss Syndrome in a 14-Year-Old Boy Diagnosed by Transbronchial Lung Biopsy. Clinical Pediatrics. 30(8). 502–505. 11 indexed citations

10.

Grody, W W, Christine Dunkel‐Schetter, Michelle Fox, et al.. (1990). PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population.. PubMed Central. 32(4). 161–176. 45 indexed citations

11.

Bass, Harold N., et al.. (1985). A family with three independent autosomal translocations associated with 7q32----7qter syndrome.. Journal of Medical Genetics. 22(1). 59–63. 34 indexed citations

12.

Bass, Harold N., Robert S. Sparkes, Barbara F. Crandall, & S. Michael Marcy. (1981). Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree. The Journal of Pediatrics. 98(4). 591–593. 20 indexed citations

13.

Bass, Harold N., et al.. (1978). 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?. Journal of Medical Genetics. 15(5). 391–395. 6 indexed citations

14.

Crandall, Barbara F., et al.. (1974). The trisomy 8 syndrome: two additional mosaic cases. Journal of Medical Genetics. 11(4). 393–398. 19 indexed citations

15.

Bass, Harold N.. (1974). Hand-Foot Syndrome and Streptococcal Sepsis. Archives of Pediatrics and Adolescent Medicine. 128(5). 743–743. 2 indexed citations

16.

Bass, Harold N., Barbara F. Crandall, & S. Michael Marcy. (1973). Two different chromosome abnormalities resulting from a translocation carrier father. The Journal of Pediatrics. 83(6). 1034–1038. 24 indexed citations

17.

Bass, Harold N.. (1968). "Bubble Bath'' as an Irritant to the. Clinical Pediatrics. 7(3). 174–174. 6 indexed citations

18.

Bass, Harold N.. (1968). Mumps Orchitis in a Three-Year-Old Child. JAMA. 203(10). 892–892. 1 indexed citations

19.

Bass, Harold N. & Benjamin Emanuel. (1966). Nephrolithiasis in Childhood. The Journal of Urology. 95(6). 749–753. 29 indexed citations

20.

Harbers, L.H., Rick Hendrickson, Harold N. Bass, & Willard J. Visek. (1963). Effect of Urease Immunity upon Rats with Controlled Vitamin A Intakes. Experimental Biology and Medicine. 113(2). 420–424. 5 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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