John L. Hamerton

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John L. Hamerton

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John L. Hamerton's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A colchicine, hypotonic citrate, squash sequence for mammalian chromosomes. (1956) (752)
A cytogenetic survey of 14,069 newborn infants (1975) (386)
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. (1976) (265)
Prenatal diagnosis of genetic disease in Canada: report of a collaborative study. (1976) (226)
Standardization in human cytogenetics (2004) (170)
The cytogenetics of mammalian autosomal rearrangements. (1989) (135)
Chromosome translocation as a cause of familial mongolism. (1960) (117)
Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis: Final report (1992) (111)
Chromosome studies in a neonatal population. (1972) (102)
Robertsonian translocations in man: evidence for prezygotic selection. (1968) (102)
Chromosome Polymorphism in the Common Shrew (1957) (100)
Chromosome studies in detection of parents with high risk of second child with Down's syndrome. (1961) (96)
Human genes encoding prothrombin and ceruloplasmin map to 11p11–q12 and 3q21–24, respectively (1987) (89)
CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS. (1965) (87)
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor (1985) (85)
Familial mental retardation in a family with an inherited chromosome rearrangement (1974) (75)
Genetic intersexuality in goats. (1969) (75)
Significance of Sex Chromosome Derived Heterochromatin in Mammals (1968) (72)
THE SOMATIC CHROMOSOMES OF THE HOMINOIDEA. (1963) (67)
Chromosomal Mosaicism in Diagnostic Amniotic Fluid Cell Cultures (1974) (66)
Chromosomal changes in primary and transplanted reticular neoplasms of the mouse. (1958) (66)
Sex-chromosome Abnormalities in a Population of Mentally Defective Children (1962) (63)
A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations. (1978) (61)
Cytogenetic and endocrine studies of a freemartin heifer and its bull co-twin. (1969) (59)
Differential transmission of Down's syndrome (mongolism) through male and female translocation carriers. (1961) (58)
THE LONDON CONFERENCE ON THE NORMAL HUMAN KARYOTYPE, 28TH-30TH AUGUST, 1963. (1963) (56)
Report of the Committee on the Genetic Constitution of Chromosome (1974) (54)
An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature. (1978) (50)
Down syndrome and recent demographic trends in Manitoba. (1978) (48)
A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME. (1963) (46)
IVth International Workshop on Human Gene Mapping (1977) (43)
CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES. (1965) (40)
Deletion of the short arm of chromosome No. 10. (1975) (37)
Structural gene encoding human factor XII is located at 5q33-qter (1988) (36)
The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7 (1989) (35)
Localization of the gene encoding human factor V to chromosome 1q21-25. (1988) (34)
Non-random X Chromosome Expression in Female Mules and Hinnies (1971) (33)
Sex chromatin and human chromosomes. (1961) (33)
CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS. (1965) (33)
Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis (1982) (33)
CHROMOSOMES IN MEDICINE (1962) (31)
Paris Conference (1971), supplement (1975) Standardization in human cytogenetics. (1975) (31)
Chromosome Findings in Chronic Psychotic Patients (1968) (30)
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site (1983) (29)
Report of the committee on the genetic constitution of chromosome 1. (1979) (29)
Chorionic villus sampling and amniocentesis for prenatal diagnosis (1997) (29)
Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR. (1990) (28)
G6PD Expression and X Chromosome Late Replication in Fibroblast Clones from a Female Mule (1972) (27)
Isolation and characterization of an α-satellite repeated sequence from human chromosome 22 (2004) (26)
Report of the Committee on the Genetic Constitution of Chromosome 1. (1978) (26)
Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes. (1991) (26)
Regional localization of 18 human X-linked DNA sequences. (1986) (25)
Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids. (1975) (24)
Characteristics of an HPRT-deficient chinese hamster cell line. (1974) (23)
Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. (1986) (23)
Somatic Chromosomes of the Gorilla (1961) (23)
Books and Monographs (1969) (23)
Human cytogenetics : general cytogenetics (1971) (22)
PROGENY OF D/G TRANSLOCATION HETEROZYGOTES IN FAMILIAL DOWN'S SYNDROME (1962) (22)
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. (1987) (22)
Immunogenetics of sex determination of the polled goat. (1980) (22)
Isolation and characterization of a processed gene for human ceruloplasmin. (1987) (22)
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)
Chromosomal localization and structure of the human P1 protamine gene. (1989) (20)
The association of glucose phosphate isomerase expression with human chromosome 19 using somatic cell hybrids (1973) (18)
The gene for clotting factor 10 is mapped to 13q32----qter. (1986) (18)
Physical and psychologic parameters in children with sex chromosome anomalies: further follow-up from the Winnipeg Cytogenetic Study of 14,069 newborn infants. (1986) (17)
A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies. (1982) (17)
A DNA marker for human chromosome 8 that detects alleles of differing sizes. (1986) (17)
Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (16)
Report of the Committee on Chromosome Markers. (1975) (16)
DETECTION AND CROSS‐REACTION OF H‐Y ANTIGEN BY HAEMAGGLUTINATION (1978) (16)
Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1. (1988) (15)
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy (1978) (15)
C-band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population (1979) (14)
Tertiary trisomy 14: is there a syndrome? (1976) (13)
Human Radiation Cytogenetics (1968) (13)
Assignment of three human gene loci to regions of chromosome 2. (1975) (13)
Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR). (1991) (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)
A 48,XXXX female (1974) (12)
Mapping the human 5S RNA genes on chromosome 1 using translocations. (1975) (12)
Fetal sex. (1970) (12)
Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists. (1991) (11)
Homozygous Robertsonian translocations in a fetus with 44 chromosomes (1982) (11)
An intersex goat with a bilaterally asymmetrical reproductive tract. (1968) (11)
Limb defects and chorionic villus sampling (1996) (11)
Paris Conference (1971): standardization in human cytogenetics. (1972) (11)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
Collaborative studies in prenatal diagnosis of chromosome aberrations (1984) (10)
A summary of the human gene map, 1973-1977. (1978) (10)
Human population cytogenetics: dilemmas and problems. (1976) (10)
The Chromosome Disorders. An Introduction for Clinicians (1967) (10)
Evidence for the role of the maternal immune system in balancing the sex ratio in mice. (1980) (9)
Investigation of the origin of variant, truncated estrogen receptor-like mRNAs identified in some human breast cancer biopsy samples (2004) (9)
Special Notice to Contributors and Subscribers (1976) (9)
Chapter 6 – ABNORMALITIES OF THE AUTOSOMES–GROUP E (16–18 GROUP–DENVER CONFERENCE) (1971) (9)
Proline incorporation by cultured skin fibroblasts from patients with Duchenne muscular dystrophy (1982) (9)
Cytogenetic characteristics of 26 polyethylene glycol-induced human-hamster hybrid cell lines. (1979) (9)
Prenatal diagnosis in Canada — 1990: A review (1994) (9)
Human gene mapping 4 : Winnipeg conference (1977), fourth International Workshop on Human Gene Mapping (1978) (8)
Searching for Molecular Abnormalities in Genetic Diseases by the Use of a Double Labeling Technique. II. Deficiency of a Basic Protein in Fibroblasts of Patients with Pompe's Disease (1978) (7)
Banding patterns of metaphase chromosomes in Down's syndrome. (1971) (7)
Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter→q21 (1980) (7)
Children and young adults with sex chromosome aneuploidy : follow-up, clinical, and molecular studies : proceedings of the 5th International Workshop on Sex Chromosome Anomalies held at Minaki, Ontario, Canada, June 7-10, 1989 (1991) (7)
Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in man. (1976) (7)
Chapter 2 – ABNORMAL SEX CHROMOSOME COMPLEMENTS IN THE FEMALE (1971) (6)
Non-random Inactivation of the X Chromosome in the Female Mule (1970) (6)
A MONGOL CHILD WITHOUT TRISOMY G. (1965) (6)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
Chapter 5 – AUTOSOMAL ABNORMALITIES–GROUP G (1971) (6)
A BglII RFLP at the human prolactin gene locus on chromosome 6 (PRL). (1991) (6)
Report of the committee on the genetic constitution of chromosomes 1 and 2. (1975) (6)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
Sex chromosome anomalies: prenatal diagnosis and the need for continued prospective studies. (1990) (5)
Chapter 9 – CYTOGENETICS OF HUMAN PREGNANCY WASTAGE (1971) (5)
Proceedings: Synteny of the IDH-1 and MDH-1 gene loci in man and probable assignment to chromosome 2. (1974) (5)
DOWN'S SYNDROME (MONGOLISM) WITH NORMAL CHROMOSOMES (1962) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study. (1979) (5)
Mapping the human 5S RNA genes on chromosome 1 using translocations. (1975) (5)
4 – MAMMALIAN SEX CHROMOSOMES (1958) (5)
Analyses of data on rates of cytogenetic disorders in live births. (1978) (5)
Constitutive heterochromatin in mouse chromosomes treated with typsin. (1973) (5)
Human chromosomes control growth of human-chinese hamster somatic cell hybrids (1982) (4)
The effect of gamma irradiation of human cells and somatic cell hybridization on sister chromatid exchange frequencies in the hamster chromosomes of hamster-human hybrid lines. (1981) (4)
Localization of the processed gene for human ceruloplasmin to chromosome region 8q21.13----q23.1 by in situ hybridization. (1988) (4)
Cytogenetic disorders. (1984) (4)
Chapter 3 – THE SEX CHROMOSOMES AND INTERSEXUALITY IN MAN (1971) (4)
TaqI and RsaI RFLP's at the prolactin inducible protein (PIP) locus on chromosome 7. (1989) (4)
The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids. (1981) (4)
Chapter 10 – CHROMOSOMES AND NEOPLASTIC DISEASE (1971) (4)
Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome (1991) (4)
The H-Y antigen:production of antibodies, detection, and cross-reaction between mouse, rat, and human. (1978) (4)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
Defining the chromosomal basis of mental handicap (1999) (4)
The characteristics of a population of Canadian women offered maternal serum alphafetoprotein screening during pregnancy. (1986) (3)
Section 2: Chromosome disease (1981) (3)
Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons. (1992) (3)
Heterogeneity in the biochemical characteristics of red blood cell hypoxanthine-guanine phosphoribosyl transferase from two unrelated patients with the lesch-nyhan syndrome (1973) (3)
Conformation of the assignment of a glutathione peroxidase locus to chromosome 3 in man. (1979) (3)
Proceedings: Localization of the structural gene for human peptidase-A to chromosome 18. (1974) (3)
A ribulose 5-phosphate 3-epimerase (RPE) locus is on human chromosome 2. (1982) (3)
Translocation in Human Chromosomes with Special Reference to Mental Retardation and Congenital Malformations (1968) (3)
Human phosphoglycolate phosphatase is coded by a gene on chromosome 16. (1980) (3)
Workshop on collaborative studies in prenatal diagnosis of chromosome disease. (1982) (2)
Chapter 8 – ABNORMALITIES OF THE AUTOSOMES: TRISOMICS, DELETIONS, DUPLICATIONS, AND TRANSLOCATIONS (EXCEPT GROUPS D, E, AND G) (1971) (2)
Physical and psychological findings in adolescents with sex chromosome abnormalities ascertained in the Winnipeg Cytogenetic Study of Newborns: 1970-1973. (1990) (2)
Proposed banding nomenclature for the Chinese hamster chromosomes (Cricetulus grises). (1976) (2)
Human cytogenetic registries (1975) (2)
Chapter 4 – SEX DETERMINATION AND THE SIGNIFICANCE OF THE SEX CHROMOSOME ABNORMALITIES IN MAN AND MAMMALS (1971) (2)
Clonal culture of human amniocytes. (1982) (2)
Assignment of the inorganic pyrophosphatase gene locus (PP) to chromosome 10 in man. (1976) (2)
Intracellular Localization of Four Dehydrogenases in Human Skin Fibroblasts in Tissue Culture (1964) (2)
Chromosomal localization of a sequence with in vivo activity for initiation of DNA replication (1993) (2)
Report of the committee on the genetic constitution of chromosome 1. (1982) (2)
Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter leads to q21. (1980) (2)
Tentative assignment of the peptidase-A (Pep-A) gene locus to the (q21-qter) region of chromosome 18 in man. (1975) (2)
Human Population Cytogenetics (1968) (1)
Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
Chicago Conference 1966: Standardization in Human Cytogenetics (1967) (1)
Ethical considerations in newborn chromosome screening programs. (1979) (1)
Localization of gene loci on chromosome 12 and the X in man. (1975) (1)
Demonstration of fluorescent X and Y bodies after antibody- and complement-mediated cytotoxicity (1977) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Further data on the assignment of the phosphoglucomutase2 (PGM2) gene locus to chromosome 4 in man. (1975) (1)
Long-term lymphocyte cultures--cytogenetics. (1973) (1)
Assignment of three human gene loci to regions of chromsome 2. (1975) (1)
CHORIONIC VILLUS SAMPLING VERSUS AMNIOCENTESIS (1989) (1)
Report of the committee on the genetic constitution of chromosome 1. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (1)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Familial chromosomal aberrations and metabolic disorders. (1992) (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)
Rapide Mbeddinogf Minuteo Bjectisn Paraffin (1956) (1)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Subject Index Vol. 22, 1978 (1978) (0)
References to the committee reports (1975) (0)
[No Title] (1969) (0)
Cardiomyopathy in duchenne/becker muscular dystrophy: Gene analysis with DNA probesclose to the disease locus * (1986) (0)
Incorporation of methionine sulphur into cysteine in vitro by fibroblasts deficient in cystathionine synthetase. (1969) (0)
Note to contributors and readers (1974) (0)
Contents, Vol. 37, 1984 (1984) (0)
Human Cytogenetics (1961) (0)
The William Allan Memorial Award. Presented to Patricia A. Jacobs, D.Sc., at the annual meeting of the American Society of Human Genetics, Dallas, October 28-31, 1981. (1982) (0)
Assignment of the inorganic chromosome 10 in man. (1976) (0)
Deletion of the Long Arms of Chromosome 18 (46,XX,18q-) Associated with Absence of IgA and Hypothyroidism in an Adult (2006) (0)
Books and Monographs (1968) (0)
Fetal karyotype of amniotic cells without culturing. (1972) (0)
The human complement after trypsin pretreatment as compared to the Paris standard (1975) (0)
Report of the committee on the genetic constitution of chromosome 1. (1980) (0)
Regional localizations of four markers on chromosome 1 using a 1/4 translocation. (1976) (0)
Contents, Vol. 32, 1982 (1982) (0)
Subject Index Vol. 32, 1982 (1982) (0)
Characterization of cDNA Clones Corresponding to Genomic Loci Rearranged in Patients with Prader-Willi Syndrome (1992) (0)
Painter, Theophilus Schickel (2001) (0)
Contents, Vol. 24, 1979 (1974) (0)
Obituary (1888) (0)
Catalog of mapped human gene markers. (1980) (0)
Chromosomes and Genes. The Biological Basis of Heredity (1970) (0)
The Handling of Chromosomes (1970) (0)
Proceedings: Report of the Committee on the Genetic Constitution of Chromosome 1. (1974) (0)
THE HUMAN X CHROMOSOME (1962) (0)
Subject Index Vol. 20, 1978 (1978) (0)
Sex Chromosomes (1968) (0)
Annex 8: Familial chromosomal aberrations and metabolic disorders (1992) (0)
Chromosomes in Medicine (1962) (0)
The Elements of Cytogenetics (1970) (0)
Regional localization of four markers on chromosome 1 using 1/4 translocation. (1976) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
The Genetical Society of Great Britain Abstracts of Papers read at the hundred and fifty-eighth meeting of the Society held on 8th and 9th November 1968, at the University College, London (1969) (0)
Books and Monographs (1969) (0)
Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7. (1987) (0)
LYONISATION OF THE X CHROMOSOME. (1964) (0)
The association of glucose phasphate isomerase expression with human chromosome 19 using somatic cell hybrids. (1973) (0)
The human X chromosome. (1990) (0)
An Atlas of Mammalian Chromsomes, Vol. 1 (1968) (0)
Subject Index Vol. 47, 1988 (1988) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Human Afflictions and Chromosome Abberations (1970) (0)
Contents, Vol. 47, 1988 (1988) (0)
In Reply: CHROMOSOME ABNORMALITIES IN PSYCHIATRIC PATIENTS (1969) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Effects of radiation of human-Chinese hamster somatic cell hybrids (1979) (0)
Peter John Langford Cook, BA, MB Cantab., PhD Lond. (1982) (0)
Further data on the assignment of the phosphoglucomutase (PGM2) gene locus to chromosome 4 in man. (1975) (0)
The Chromosomes of the Hominoidea (2017) (0)
CHORIONIC VILLUS SAMPLING AND EARLY AMNIOCENTESIS FOR PRENATAL DIAGNOSIS. AUTHORS' REPLY (1997) (0)
Subject Index Vol. 24, 1979 (1979) (0)
Chorionic villus sampling and early amniocentesis for prenatal diagnosis (1997) (0)
Standard chromosome nomenclature (1981) (0)
Introduction (1981) (0)

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John L. Hamerton is affiliated with the following schools:

University of Manitoba

John L. Hamerton's Academic­Influence.com Rankings

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John L. Hamerton's Published Works

Published Works

What Schools Are Affiliated With John L. Hamerton?

John L. Hamerton's AcademicInfluence.com Rankings