H. Bullman - Concepedia

Author

H. Bullman

Also Known As

Bullman, H., H Bullman, H. BULLMAN, H. Bullman, H. M. S. BULLMAN, Hilary Bullman, Hilary M. S. Bullman, Hilary M.S. Bullman

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Princess Anne Hospital Wessex Regional Genetics Laboratory Salisbury District Hospital University of Southampton Institute of Cancer Research

About

H. Bullman is an author at Princess Anne Hospital specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	913
2	Cell Biology	3	3	135
3	Natural Sciences	2	2	109
4	Engineering	1	1	46
5	Biomolecular Engineering	1	1	46

H. Bullman

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse Elisabeth H. Weiss, Lynn Golden, Karen Fahrner, Nature HistocompatibilityChromatinKnockout MouseDevelopmental BiologyGenetics	1984	323
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. Diana Eccles, Rob B. van der Luijt, Cor Breukel, PubMed	1996	193
Duplication of 7p12.1-p13, including GRB10 and IGFBP1 , in a mother and daughter with features of Silver-Russell syndrome Christine A Joyce, Andrew J. Sharp, Jamie M. Walker, Human Genetics Silver-russell SyndromeDevelopmental BiologyGenetic DisorderGeneticsPathology	1999	116
Population studies of the fragile X: a molecular approach. P. A. Jacobs, H. Bullman, Janet L. Macpherson, Journal of Medical Genetics Genome InstabilityGenetic TestingMental ImpairmentFragile XCytogenetics	1993	107
Expression of marine H–2Kb histocompatibility antigen in cells transformed with cloned H–2 genes A. L. Mellor, L. Golden, Elisabeth H. Weiss, Nature HistocompatibilityCloned H–2 GenesHuman Leukocyte AntigenImmunologyAntigen Processing	1982	104
Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver–Russell syndrome H. Bullman, Margaret Lever, David Robinson, Journal of Medical Genetics	2008	102
Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci Claire Turner, Deborah Mackay, Jonathan L A Callaway, European Journal of Human Genetics ChromatinMethylation ChangeDevelopmental BiologyMedicineGenetics	2010	97
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation James Macpherson, H. Bullman, Sheila Youings, Human Molecular Genetics	1994	87
Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14 I. Karen Temple, V Shrubb, Margaret Lever, Journal of Medical Genetics CytogeneticsEpigenetic ChangeGeneticsClinical PresentationGynecology	2007	63
Cloning and Expression of the Erwinia chrysanthemi Asparaginase Gene in Escherichia coli and Erwinia carotovora Harry J. Gilbert, Richard Blazek, H. Bullman, Microbiology BiosynthesisEngineeringErwinia CarotovoraErwinia EnzymeGenetics	1986	46

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