H. Bullman

1.5k total citations
23 papers, 1.1k citations indexed

About

H. Bullman is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H. Bullman has authored 23 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H. Bullman's work include Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (7 papers) and Prenatal Screening and Diagnostics (5 papers). H. Bullman is often cited by papers focused on Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (7 papers) and Prenatal Screening and Diagnostics (5 papers). H. Bullman collaborates with scholars based in United Kingdom, Malaysia and Slovakia. H. Bullman's co-authors include I. Karen Temple, Elisabeth H. Weiss, Richard A. Flavell, Margaret Lever, James J. Devlin, Andrew L. Mellor, Harm A.W.M. Tiddens, Karen Fahrner, Sheila Youings and Deborah Mackay and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

H. Bullman

23 papers receiving 1.0k citations

Peers

H. Bullman

GENET

IMMUN

PPCH

PFM

N. Yannoutsos United Kingdom

Marga Belle White United States

Gaël A. Millot France

John Melnyk United States

Joel Geoghegan United States

Ildikó Győry Germany

Jorge Luis Valdés González United States

A. J. Therkelsen Denmark

Corinne Wong United States

P Franceschini Italy

N. Yannoutsos United Kingdom

H. Bullman

1.0k ×1.7

463 ×0.8

GENET

297 ×1.3

IMMUN

68 ×0.3

PPCH

15 ×0.1

PFM

Citations per year, relative to H. Bullman H. Bullman (= 1×) peers N. Yannoutsos

Countries citing papers authored by H. Bullman

Since Specialization

Citations

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

Fields of papers citing papers by H. Bullman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Bullman

This figure shows the co-authorship network connecting the top 25 collaborators of H. Bullman. A scholar is included among the top collaborators of H. Bullman 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 H. Bullman. H. Bullman 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

Dixit, Abhijit, Kate Chandler, Margaret Lever, et al.. (2012). Pseudohypoparathyroidism Type 1b due to Paternal Uniparental Disomy of Chromosome 20q. The Journal of Clinical Endocrinology & Metabolism. 98(1). E103–E108. 61 indexed citations

Bunyan, David J., et al.. (2011). Different denaturation rates between methylated and non-methylated genomic DNA can result in allele-specific PCR amplification. ePrints Soton (University of Southampton). 1(2). 13–14. 4 indexed citations

Turner, Claire, Deborah Mackay, Jonathan L A Callaway, et al.. (2010). Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. European Journal of Human Genetics. 18(6). 648–655. 73 indexed citations

Temple, I. Karen, et al.. (2009). Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14. BMJ Case Reports. 2009. bcr0620091997–bcr0620091997. 3 indexed citations

Bullman, H., Margaret Lever, David Robinson, et al.. (2008). Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver–Russell syndrome. Journal of Medical Genetics. 45(6). 396–399. 64 indexed citations

Staník, Juraj, Sarah E. Flanagan, Daniela Gašperíková, et al.. (2008). Coincidence of a Novel KCNJ11 Missense Variant R365H With a Paternally Inherited 6q24 Duplication in a Patient With Transient Neonatal Diabetes. Diabetes Care. 31(9). 1736–1737. 1 indexed citations

Temple, I. Karen, et al.. (2007). Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14. Journal of Medical Genetics. 44(10). 637–640. 48 indexed citations

Cox, Helen, H. Bullman, & I. Karen Temple. (2003). Maternal UPD(14) in the patient with a normal karyotype: Clinical report and a systematic search for cases in samples sent for testing for Prader–Willi syndrome. American Journal of Medical Genetics Part A. 127A(1). 21–25. 24 indexed citations

Joyce, Christine A, Andrew J. Sharp, Jamie M. Walker, H. Bullman, & I. Karen Temple. (1999). Duplication of 7p12.1-p13, including GRB10 and IGFBP1 , in a mother and daughter with features of Silver-Russell syndrome. Human Genetics. 105(3). 273–280. 79 indexed citations

10.

Joyce, Christine A, et al.. (1999). Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Human Genetics. 105(3). 273–280. 7 indexed citations

11.

Eccles, Diana, Rob B. van der Luijt, Cor Breukel, et al.. (1996). Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.. PubMed. 59(6). 1193–201. 138 indexed citations

12.

Macpherson, James, H. Bullman, Sheila Youings, & Patricia A. Jacobs. (1994). Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation. Human Molecular Genetics. 3(3). 399–405. 69 indexed citations

13.

Jacobs, P. A., H. Bullman, Janet L. Macpherson, et al.. (1993). Population studies of the fragile X: a molecular approach.. Journal of Medical Genetics. 30(6). 454–459. 88 indexed citations

14.

Brehm, John K., et al.. (1992). Physical characterization of the replication origin of the cryptic plasmid pCB101 isolated from Clostridium butyricum NCIB 7423. Plasmid. 28(1). 1–13. 6 indexed citations

15.

Gilbert, Harry J., et al.. (1986). Cloning and Expression of the Erwinia chrysanthemi Asparaginase Gene in Escherichia coli and Erwinia carotovora. Microbiology. 132(1). 151–160. 39 indexed citations

16.

Weiss, Elisabeth H., Karen Fahrner, Andrew L. Mellor, et al.. (1984). Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse. Nature. 310(5979). 650–655. 277 indexed citations

17.

Bullman, H., Meinrad Busslinger, E. deBoer, et al.. (1982). The structure and expression of mammalian gene clusters.. PubMed. 103 Pt A. 37–55. 2 indexed citations

18.

Golden, L., Elisabeth H. Weiss, H. Bullman, et al.. (1982). Expression of marine H–2Kb histocompatibility antigen in cells transformed with cloned H–2 genes. Nature. 298(5874). 529–534. 89 indexed citations

19.

Nery, Rosane Maria, et al.. (1974). Isolation and Partial Characterization of Macromolecular Urinary Aggregates Containing Carcinoembryonic Antigen-Like Activity. British Journal of Cancer. 29(6). 413–424. 9 indexed citations

20.

Nery, Rosane Maria, Adel L. Barsoum, H. Bullman, & Alan Nevill. (1974). Carcinoembryonic antigen-like substances of human urothelial carcinomas. Isolation of components from pathological urine and comparison with colorectal carcinoma antigens. Biochemical Journal. 139(2). 431–440. 12 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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