Phyllis McAlpine
Canadian geneticist
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Why Is Phyllis McAlpine Influential?
(Suggest an Edit or Addition)According to Wikipedia, Phyllis Jean McAlpine was a Canadian geneticist. She was a pioneer in mapping the human genome and served as Chair of the HUGO Gene Nomenclature Committee. Education McAlpine was awarded an honours bachelor's degree at Western University where she won a gold medal in zoology. She received a master's degree from the University of Toronto in 1966. Her thesis was called An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy. She went on to complete a PhD at University College London in 1970 with a thesis entitled Studies on the genetic variation of phosphoglucomutase in man. McAlpine was mentored and supervised by women in her field throughout her education. Her undergraduate work was performed under Helen Battle, and Margaret Thompson was her advisor in Toronto. Her PhD supervisor was Harry Harris.
Phyllis McAlpine's Published Works
Published Works
- International system for human gene nomenclature (1979) ISGN (1979). (1979) (161)
- Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). (1987) (138)
- The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26. (1991) (109)
- Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee. (1997) (104)
- An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy. (1967) (82)
- Detection of attograms of antigen by a high-sensitivity enzyme-linked immunoabsorbent assay (HS-ELISA) using a fluorogenic substrate. (1980) (79)
- Familial mental retardation in a family with an inherited chromosome rearrangement (1974) (75)
- Report of the nomenclature committee and the 1989 catalog of mapped genes. (1989) (59)
- The 1991 catalog of mapped genes and report of the nomenclature committee (Part 1 of 5) (1991) (58)
- The 1990 catalog of mapped genes and report of the nomenclature committee. (1990) (54)
- The 1985 Catalog of Mapped Genes and report of the Nomenclature Committee. (1985) (53)
- Thermostability studies on the isozymes of human phosphoglucomutase (1970) (49)
- Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1979) (44)
- International System for Human Gene Nomenclature (1979) ISGN (1979). (1980) (39)
- The 1983 catalogue of mapped human genetic markers and report of the Nomenclature Committee. (1982) (38)
- Genetic markers in blood in a Canadian Eskimo population with a comparison of allele frequencies in circumpolar populations. (1974) (38)
- Nomenclature of human DNA repair genes. (1994) (36)
- The 1979 catalog of human genes and chromosome assignments. (1979) (34)
- Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17. (1990) (30)
- An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa. (1985) (29)
- The 1988 catalog of mapped genes and report of the nomenclature committee. (1988) (27)
- The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 1 of 4) (1987) (25)
- Genetic diversity among Canadienne, Brown Swiss, Holstein, and Jersey cattle of Canada based on 15 bovine microsatellite markers. (2002) (25)
- Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. (1986) (25)
- A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy. (1977) (24)
- Abstracts of workshop presentations (Part 13 of 13) (1985) (23)
- Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells. (1973) (21)
- Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
- Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
- Nomenclature for human homeobox genes. (1990) (18)
- Brief clinical report: ring chromosome 17 in a mentally retarded young man - clinical, cytogenetic, and biochemical investigations. (1982) (18)
- Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (16)
- Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1. (1988) (15)
- Multiplicity of genetic polymorphisms of blood in the Schmiedeleut Hutterites. (1985) (14)
- Coagulation factor XIII B subunit is encoded by a gene linked to the regulator of complement activation (RCA) gene cluster in man (2004) (14)
- The 1987 Catalog of mapped genes and report of the nomenclature committee. (1987) (13)
- Assignment of three human gene loci to regions of chromosome 2. (1975) (13)
- Tertiary trisomy 14: is there a syndrome? (1976) (13)
- Abstracts of workshop presentations (Part 1 of 13) (1985) (13)
- The 1979 catalog of human genes and chromosome assignments. (1980) (13)
- The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee. (1982) (13)
- A ‘New’ Blood Group Antigen Fra: Incidence, Inheritance and Genetic Linkage Analysis 1 (1978) (12)
- ISOZYME ANALYSIS OF SOMATIC CELL HYBRIDS: ASSIGNMENT OF THE PHOSPHOGLUCOMUTASE 2 ( PGM 2 ) GENE LOCUS TO CHROMOSOME 4 IN MAN WITH DATA ON THE MOLECULAR STRUCTURE AND HUMAN CHROMOSOME ASSIGNMENTS OF SIX ADDITIONAL MARKERS (1975) (12)
- Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markers. (1985) (12)
- Is the DIA1 locus linked to the P blood group locus? (1978) (12)
- Abstracts of workshop presentations (Part 9 of 13) (1985) (10)
- Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
- Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
- The 1991 catalog of mapped genes and report of the nomenclature committee (Part 5 of 5) (1991) (9)
- Abstracts of workshop presentations (Part 12 of 13) (1985) (9)
- The catalog of human genes and chromosome assignments. A report on human genetic nomenclature and genes that have been mapped in man. (1978) (8)
- Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
- The Swann Phenotype 700:4,‐41; Genetic Studies (1988) (7)
- Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
- The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs. (1991) (7)
- Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16. (1988) (7)
- Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (7)
- Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
- Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
- Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
- Complementation by two non-homologous recombinant chromosomes 3. (1991) (5)
- Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
- Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
- Proceedings: Synteny of the IDH-1 and MDH-1 gene loci in man and probable assignment to chromosome 2. (1974) (5)
- Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
- Genetic nomenclature guide. Human. (1995) (5)
- Abstracts of workshop presentations pp. 948-967 (1989) (5)
- Fertility and other demographic aspects of the Canadian Eskimo communities of Igloolik and Hall Beach. (1976) (5)
- Assignment of the gene(s) governing Froese and Swann blood group polymorphism to chromosome 17q (1996) (5)
- Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
- Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
- Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
- Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
- The LW: C3 recombination fraction in female meioses (1987) (4)
- Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
- Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
- Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
- Abstracts of workshop presentations (Part 11 of 13) (1985) (3)
- Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
- Proceedings: Localization of the structural gene for human peptidase-A to chromosome 18. (1974) (3)
- Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
- Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
- Identification of an uncommon haptoglobin type using DNA and protein analysis (1993) (3)
- The Colton blood group locus (1988) (3)
- A PstI polymorphism in the human coagulation factor V (F5) gene. (1990) (3)
- Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
- Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
- Proceedings: Exclusion of peptidase-A structural gene locus from the q11q21 region of chromosome 18 in man. (1974) (2)
- Genetic diversity among Canadienne, Brown Swiss, Holstein and Jersey cattle based on mitochondrial D-loop sequence variation (2003) (2)
- A “new” low incidence red cell antigen, NFLD (2004) (2)
- Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21-qter) region of chromosome 18 in man. (1975) (2)
- Polymorphism detected by multiple RENS in the human coagulation factor II (F2) gene (1991) (2)
- Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
- Assignment of the inorganic pyrophosphatase gene locus (PP) to chromosome 10 in man. (1976) (2)
- Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
- Abstracts of workshop presentations (Part 4 of 13) (1985) (2)
- Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter: F13A:HLA:GL01:cen gene order (1988) (2)
- An immunochemical method for the detection of the expression of human gene loci in human-rodent somatic cell hybrids with special reference to the GPI locus (1976) (1)
- Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
- Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21 leads to qter) region of chromosome 18 in man. (1975) (1)
- Abstracts of workshop presentations (Part 7 of 13) (1985) (1)
- Exclusion of the Red Blood Cell Antigen Fra from the Colton Blood Group System (1980) (1)
- Contents Vol. 55, 1990 (1990) (1)
- Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
- Workshop on mapping by classical methods. (1982) (1)
- Multifractal analysis of DNA (1998) (1)
- Abstracts of workshop presentations (Part 5 of 13) (1985) (1)
- Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
- Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
- Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual. (1983) (1)
- Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
- Assignment of three human gene loci to regions of chromsome 2. (1975) (1)
- Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
- Abstracts of workshop presentations (Part 6 of 13) (1985) (1)
- Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1982) (1)
- Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man. (1975) (1)
- More about use of the term Drb (1993) (1)
- Guidelines for Human Gene Mapping (1997) (1)
- Abstracts of workshop presentations (Part 2 of 13) (1985) (1)
- Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
- The 1991 catalog of mapped genes and report of the nomenclature committee (Part 3 of 5) (1991) (0)
- The 1991 catalog of mapped genes and report of the nomenclature committee (Part 2 of 5) (1991) (0)
- Subject index Vol. 46, 1987 (1987) (0)
- A note on the use of HGML LIT literature file numbers (1989) (0)
- Abstracts of workshop presentations (Part 8 of 13) (1985) (0)
- Assignment of the inorganic chromosome 10 in man. (1976) (0)
- Contents, Vol. 37, 1984 (1984) (0)
- Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. (1980) (0)
- Regional localizations of four markers on chromosome 1 using a 1/4 translocation. (1976) (0)
- The 1991 catalog of mapped genes and report of the nomenclature committee (Part 4 of 5) (1991) (0)
- Catalog of mapped human gene markers. (1980) (0)
- Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 2 of 3) (1989) (0)
- Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
- An assessment of the in the detection of carriers muscular dystrophy creatine kinase test of Duchenne (1967) (0)
- What's in a name? (1990) (0)
- Subject Index Vol. 32, 1982 (1982) (0)
- Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
- Subject index Vol. 40, 1985 (1985) (0)
- The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 3 of 4) (1987) (0)
- LETTER TO THE EDITOR Nomenclature for Human Homeobox Genes (1990) (0)
- Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 3 of 3) (1989) (0)
- Gpt lies outside inversion 8 p23q22 in the human genome (1984) (0)
- Subject Index Vol. 25, 1979 (1979) (0)
- Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
- Contents, Vol. 32, 1982 (1982) (0)
- Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
- Regional localization of four markers on chromosome 1 using 1/4 translocation. (1976) (0)
- The 1990 catalog of mapped genes and report of the nomenclature committee (Part 2 of 3) (1990) (0)
- The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 4 of 4) (1987) (0)
- Further data on the assignment of the phosphoglucomutase (PGM2) gene locus to chromosome 4 in man. (1975) (0)
- Analysis of pericentric inversions (1994) (0)
- Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
- Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
- Subject Index Vol. 16, 1976 (1976) (0)
- The 1990 catalog of mapped genes and report of the nomenclature committee (Part 3 of 4) (1990) (0)
- The 1990 catalog of mapped genes and report of the nomenclature committee (Part 4 of 4) (1990) (0)
- Index by Keyword (1989) (0)
- Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
- Subject Index Vol. 22, 1978 (1978) (0)
- Index by Abstract Number (1989) (0)
- Familial pericentric inversion of chromosome 11detected prenatally (1981) (0)
- Abstracts of workshop presentations (Part 10 of 13) (1985) (0)
- Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
- The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
- References to the committee reports (1975) (0)
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