Jan E. Lindsten

Q: What Schools Are Affiliated With Jan E. Lindsten

Jan E. Lindsten is affiliated with the following schools: University of Oxford, Stanford University, University of California, San Francisco, Karolinska Institute

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Jan E. Lindsten

Philosophy

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#11377

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Logic

#5095

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#6457

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Jan E. Lindsten

Biology

#10890

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#14250

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Physiology

#342

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#557

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biology Degrees

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Jan E. Lindsten'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

The Nobel Prize in Physiology or Medicine (2001) (378)
MATERNAL SMOKING DURING PREGNANCY AND RISK OF CHILDHOOD CANCER (1986) (213)
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis. (1970) (176)
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture. (1981) (170)
CHROMOSOME ABERRATIONS AND SISTER-CHROMATID EXCHANGE IN WORKERS IN CHEMICAL LABORATORIES AND A ROTOPRINTING FACTORY AND IN CHILDREN OF WOMEN LABORATORY WORKERS (1977) (164)
Chromosomal abnormalities in father and Mongol child. (1960) (157)
A child with 49 chromosomes. (1960) (155)
A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquin (1985) (152)
European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures (1984) (133)
Chromosome breakage in humans exposed to methyl mercury through fish consumption. Preliminary communication. (1970) (121)
Dermatoglyphic anomalies in Turner's syndrome (1964) (112)
The 11q;22q translocation: A European collaborative analysis of 43 cases (2004) (109)
Bromodeoxyuridine-induced sister chromatid exchanges in human lymphocytes. (2009) (104)
Cytogenetical observations in mongolism. (1959) (104)
A mapping function for man. (1977) (102)
CHROMOSOME ABERRATIONS IN WORKERS EXPOSED TO VINYL CHLORIDE (1975) (101)
Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques. (1972) (101)
Fluorescent staining of heteropycnotic chromosome regions in human interphase nuclei. (1970) (99)
Methylmercury-induced chromosome damage in man (1974) (97)
Distribution of mitomycin C induced breaks on human chromosomes. (2009) (85)
TIME OF ERUPTION OF THE PERMANENT TEETH, CEPHALOMETRIC AND TOOTH MEASUREMENT AND SULPHATION FACTOR ACTIVITY IN 45 PATIENTS WITH TURNER'S SYNDROME WITH DIFFERENT TYPES OF X CHROMOSOME ABERRATIONS. (1965) (82)
TRITIATED THYMIDINE INCORPORATION IN AN ISOCHROMOSOME FOR THE LONG ARM OF THE X CHROMOSOME IN MAN (1963) (77)
A NEW TYPE OF CHROMOSOMAL ABNORMALITY IN GONADAL DYSGENESIS (1960) (72)
Chromosome analysis of lymphocytes from cadmium workers and Itai-itai patients. (1975) (72)
Hearing impairment in Turner's syndrome. (1969) (69)
DNA repair and frequency of X‐ray and u.v.‐light induced chromosome aberrations in leukocytes from patients with Down's syndrome (1976) (68)
The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families (2004) (64)
Cytogenetic aspects of human male meiosis. (1973) (62)
Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis. (1970) (61)
SELF-PERPETUATING RING CHROMOSOME IN A PATIENT WITH GONADAL DYSGENESIS (1962) (59)
Involvement of chromosomes 8, 9, 19 and 22 in PH1 positive and PH1 negative chronic myelocytic leukemia in the chronic or blastic stage. (2009) (57)
Presumptive direct insertion within chromosome 2 in man (1973) (54)
Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics. (2009) (54)
Cytogenetical and clinical investigations in four subjects with anomalies of sexual development (1966) (53)
Incidence of Down's syndrome in Sweden during the years 1968-1977. (1981) (51)
Trisomy 21 in man due to maternal non-disjunction during the first meiotic division. (2009) (51)
Trisomy 8 in acute myeloblastic leukemia and sideroachrestic anemia. (1974) (50)
CHROMOSOME COMPLEMENT IN GONADAL DYSGENESIS (TURNER'S SYNDROME) (1959) (50)
An international system for human cytogenetic nomenclature (1978) ISCN (1978). Report of the Standing Commitee on Human Cytogenetic Nomenclature. (1978) (50)
Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis. (2009) (49)
The “Cat Eye syndrome”: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter→q11) associated with a characteristic phenotype (1981) (49)
DUPLICATION OF PART OF CHROMOSOME NO. 1 IN MYELOPROLIFERATIVE DISEASES (1978) (48)
Somatic chromosome complement in continuously cultured cells of two individuals with gonadal dysgenesis * (1959) (46)
Plasma level of growth hormone and chromosome complement in four patients with gonadal dysgenesis (Turner's syndrome). (1960) (46)
Studies on spontaneous abortions. (1973) (46)
Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis. (2009) (46)
An extra C chromosome and various metabolic abnormalities in the bone marrow from a patient with refractory sideroblastic anaemia. (2009) (44)
Presumptive X-Autosome Translocation in a Cow : Preferential Inactivation of the Normal X Chromosome (1968) (44)
Synthesis of Deoxyribonucleic Acid on X-Chromosomes of an XXXXY Male (1963) (43)
The XY bivalent in human male meiosis (1966) (42)
Segregation analysis of balanced pericentric inversions in pedigree data (1986) (42)
Presumptive isochromosomes for the long arm of X in man. Analysis of five families (1963) (41)
LINEAR GROWTH, SULPHATION FACTOR ACTIVITY AND CHROMOSOME CONSTITUTION IN 22 SUBJECTS WITH TURNER'S SYNDROME (1963) (40)
Timing of sex chromosome replication in somatic and germ-line cells of the mouse and the rat. (1967) (39)
An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. (1973) (38)
Observations on the so called sex chromatin in human somatic cells cultivated in vitro. (1959) (37)
Genetic regulation of melatonin excretion in urine (1983) (37)
Evidence that the Xg Blood Group Genes are on the Short Arm of the X chromosome (1963) (36)
Chromosomal mosaic in a girl with some features of mongolism. (1962) (36)
Genetic regulation of the kinetics of glucose‐induced insulin release in man Studies in families with diabetic and non‐diabetic probands (1985) (36)
Source of the X in XO females: the evidence of Xg. (1963) (35)
Maternal smoking and irradiation during pregnancy as risk factors for child leukemia. (1992) (35)
Rapid identification of human chromosomes by TV-techniques. (1970) (35)
Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence. (1970) (34)
Clonal origin of the Philadelphia chromosome from either the paternal or the maternal chromosome number 22. (1974) (34)
Late side effects of chemotherapy in ovarian carcinoma: A cytogenetic, hematologic, and statistical study (1982) (33)
Origin of triploidy in human abortuses. (2009) (32)
Molecular forms and activities of glycosidases in cultures of amniotic-fluid cells. (1976) (32)
MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12. (1965) (32)
A chiasma map of man. (1977) (32)
Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man (1982) (31)
Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblastic leukemia. (2009) (30)
A new variant translocation (19q+, 22q−) in chronic myelocytic leukemia (1974) (28)
A clinical and cytogenetical study of three patients with male phenotype and apparent XX sex chromosome constitution. (1966) (28)
Smoking and sister chromatid exchange. (1982) (27)
TESTICULAR GERMINAL DYSGENESIS (MALE TURNER'S SYNDROME) (1961) (27)
Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms. (1971) (26)
Changes in the incidence of Down syndrome in Sweden during 1968–1982 (1986) (26)
Etiology of Human Disease at the DNA Level (1991) (25)
Clinical and cytogenetic investigation in children of parents treated with radioiodine. (1972) (25)
The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis. (2009) (25)
HL-A Antigens and Heteromorphic Fluorescence Characters of Chromosomes in Prenatal Paternity Investigation (1972) (24)
H3-THYMIDINE UPTAKE BY A RING X CHROMOSOME IN A HUMAN FEMALE. (1964) (24)
Extra minute chromosome in somatic and germ-line cells of the same person. (1966) (23)
Physiology or Medicine (1993) (22)
THE OCCURRENCE OF ABNORMAL INSULIN AND GROWTH HORMONE (HGH) RESPONSES TO SUSTAINED HYPERCLYCAEMIA IN A DISEASE WITH SEX CHROMOSOME ABERRATIONS (TURNER'S SYNDROME) (1967) (22)
Lack of Correlation Between Contraceptive Pills and Down's Syndrome (1983) (22)
PRENATAL EVALUATION OF FETUS AT RISK FOR SEVERE VON WILLEBRAND'S DISEASE (1979) (21)
Studies on spontaneous abortions. Fluorescence analysis of abnormal karyotypes. (1973) (21)
Significance of genetic factors for the plasma insulin response to glucose in healthy subjects (1976) (20)
Genetic and environmental determinants for lipoprotein concentrations in blood. (2009) (20)
Chromosomes in leukemia (1977) (20)
A linkage study of the locus for X‐linked Charcot‐Marie‐Tooth disease (1988) (19)
Alpha fetoprotein levels in maternal serum and in amniotic fluid from early normal pregnancies (1975) (19)
The use of fluorescence techniques for the recognition of mammalian chromosomes and chromosome regions. (1972) (19)
Body height and dental development in patients with Turner's syndrome. (1974) (19)
Pathologic lysosomes and increased urinary glycosylceramide excretion in Fabry's disease. Studies on a family with evidence of linkage with the sex-linked blood group Xg. (1971) (19)
Chronology of DNA replication in the sex chromosomes of the reindeer (Rangifer tarandus L.). (1968) (19)
MATERNAL SMOKING DURING PREGNANCY AND THE RISK OF CHILDHOOD CANCER (1986) (19)
NEW TYPE OF CHROMOSOMAL MOSAICISM IN OVARIAN DYSGENESIS (1961) (19)
Chromatid interchange resulting in duplication of the short arm of chromosome number 7 in man. (1971) (18)
Nobel Lectures In Physiology Or Medicine 1971-1980 (1992) (18)
PRENATAL SEX-HORMONE EXPOSURE AND CONGENITAL LIMB-REDUCTION DEFECTS (1976) (18)
Studies on mitotic and meiotic chromosomes in subjects exposed to LSD. (1968) (18)
THE NATURE, ORIGIN, AND GENETIC IMPLICATIONS OF STRUCTURAL ABNORMALITIES OF THE SEX CHROMOSOMES IN MAN (1964) (18)
DNA CONTENT AND AREA OF SEX CHROMATIN IN SUBJECTS WITH STRUCTURAL AND NUMERICAL ABERRATIONS OF THE X CHROMOSOME. (1965) (17)
Surveillance of Down's syndrome as a paradigm of population monitoring. (1976) (17)
DNA and Chromosome Alterations in Lymphocytes of Operating Room Personnel and in Patients before and after Inhalation Anaesthesia (1982) (16)
Prenatal diagnosis of Krabbe disease (1981) (16)
An explanation of the apparently increased incidence of moderate mental retardation in Turner's syndrome (1973) (16)
EFFECTS OF SHORT TERM ADMINISTRATION OF PHYSIOLOGICAL DOSES OF HUMAN GROWTH HORMONE IN THREE PATIENTS WITH TURNER'S SYNDROME. (1964) (16)
TRISOMY 13-15. REPORT OF A CASE WITH CLINICAL, CYTOGENETIC AND PATHOLOGIC FINDINGS. (1964) (16)
Further cytogenetical observations in gonadal dysgenesis (1960) (15)
Origin of the Philadelphia chromosome. Tracing of chromosome 22 to parents of patients with chronic myelocytic leukemia. (1973) (15)
Prenatal diagnosis of Gaucher disease Assay of the ß‐glucosidase activity in amniotic fluid cells cultivated in two laboratories with different cultivation conditions (1981) (15)
The meiotic chromosomes of the male dog (Canis familiaris). (2009) (14)
A genetic analysis of the normal body‐height growth and dental development in man (1975) (14)
PRENATAL DIAGNOSIS OF CHROMOSOME ABNORMALITIES (1972) (13)
No evidence of mutations in four candidate genes for male sex determination/differentiation in sex-reversed XY females with campomelic dysplasia. (1991) (13)
Aneuploidy and polyploidy in germ-line cells of the male Chinese hamster (Cricetulus griseus). (2009) (13)
Absence of brightly fluorescent Y material in XX men. (1971) (13)
Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida (1975) (12)
Prenatal Cytogenetic Diagnosis (1974) (12)
Data and theory for a revised chiasma map of man (2004) (12)
Sex-reversed XY females with campomelic dysplasia are H-Y negative (2004) (12)
Segregation of ACP1 and MNSs in families with structural rearrangements involving chromosome 2 (1975) (12)
Unusual chromosomal mosaic (46, XX-46, XX, Cp+) in a girl with multiple malformations. (1968) (12)
SIZE OF DRUMSTICKS IN PATIENTS WITH ABNORMALITIES OF THE X-CHROMOSOME. (1964) (12)
DNA replication patterns of canine chromosomes in vivo and in vitro. (2009) (12)
Possible Localization of the Genes for the Kidd Blood Group on an Autosome Involved in a Reciprocal Translocation (1966) (12)
Congenital Malformations in Children of Mothers Aged 42 and Over (1958) (12)
Genetic regulation of melatonin excretion in urine. A preliminary report. (1983) (12)
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria (1988) (11)
Carcinoembryonic antigen in amniotic fluid. (2009) (11)
Late-replicating Y chromosome in spermatogonia of the Chinese hamster (Cricetulus griseus). (1969) (11)
Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings. (1971) (11)
The chromosomes of the Cynomolgus macaque (Macaca fascicularis). (2009) (11)
Late-replicating Y chromosome in spermatogonia of the Chinese hamster (Cricetulus griseus). (1969) (11)
Prenatal diagnosis of genetic disorders of the foetus. (1976) (11)
17. Physical Malformation and Mental Retardation in Association with Structural Autosomal Aberrations (1965) (10)
Genetic regulation of the red cell uroporphyrinogen‐l‐synthetase level in families with acute intermittent porphyria (1983) (10)
Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son. (1971) (10)
A CHILD WITH 49 CHROMOSOMES: FURTHER INVESTIGATIONS (1962) (10)
CHROMOSOME COMPLEMENT IN PARENTS OF PATIENT WITH GONADAL DYSGENESIS (TURNER'S SYNDROME) (1959) (10)
Nobel Lectures in Physiology or Medicine 1981 – 1990 (1993) (9)
Heterochromatin in preimplantation mouse embryos. (1969) (9)
The Nobel Prize in Physiology or Medicine, 1901-2000 (2000) (9)
BLOOD-SEROTONIN IN DOWN'S SYNDROME (1967) (9)
The Distribution of the Gene for the Juvenile Type of Gaucher Disease in Sweden (1989) (9)
Radiation induced chromosome aberrations in human foetal zcells grown in vitro. (1962) (8)
TRISOMY 21 OR 22 IN DOWN'S SYNDROME ? (1967) (8)
A LATE-DUPLICATING CHROMOSOME IN SPERMATOGONIAL MITOSIS OF THE MOUSE. (1965) (8)
First trimester biopsies of chorionic villi for prenatal diagnosis: experience of two laboratories (1984) (8)
Evidence for a major locus as well as a multifactorial component in the regulation of human red blood cell catechol-O-methyl-transferase activity. (1982) (8)
The history of the Nobel Prize for the discovery of insulin. (2021) (7)
The occurrence of abnormal insulin and growth hormone (HGH) responses to sustained hyperglycaemia in a disease with sex chromosome aberrations (Turner's syndrome). Including a histological study of the pancreas in two such patients. (1967) (7)
The origin and phenotype of XO males (1987) (7)
A new variant translocation (19q plus, 22q minus) in chronic myelocytic leukemia. (1974) (6)
Hearing defects in males with sex chromosome anomalies. (1971) (6)
[Prenatal diagnosis of anencephaly and spina bifida. Determination of alphafetoprotein in amniotic fluid and serum in the 16th-24th gestational week]. (1975) (6)
RELEVANCE OF MEIOTIC STUDIES IN HUMAN CHROMOSOME IDENTIFICATION (1968) (6)
Protein-heparin complexes as a cause of artificial enzyme polymorphism. (1971) (5)
The chromosomes of the Alpine marmot Marmota marmota L. (Rodentia: Sciuridae). (2009) (5)
Additional G-like chromosome in a malformed boy. (1971) (5)
Birth weight and related variables for offspring of mothers aged 42 or more years (1962) (5)
Correlation between the number of sex chromosomes and the H-Y antigen titer (2004) (5)
Protein binding of ampicillin. Path analysis of a twin material. (2009) (5)
Role of chorion villi biopsy in prenatal diagnosis of genetic disorders. (1985) (4)
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction (1990) (4)
Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18. (1972) (4)
Editorial: The Philadelphia chromosome and chronic myelocytic leukemia (CML) --still a complex relationship? (2009) (4)
Assay of the β‐glucosidase activity with natural labelled and artificial substrates in cultivated skin fibroblasts from homozygotes and heterozygotes with the Norrbottnian type of Gaucher disease (1980) (4)
CYTOGENETICAL AND CLINICAL INVESTIGATIONS IN PATIENTS WITH TURNER'S SYNDROME. (1965) (4)
[Prenatal diagnosis of anencephalus and spina bifida by determination of alphafetoprotein]. (1975) (4)
Section 2: Chromosome disease (1981) (3)
Dental maturity as a measure of somatic development in children. (1978) (3)
An early behavioral description of a person with Turner's syndrome (1978) (3)
Chromosome studies in Laurence-Moon-Biedl's syndrome. (1961) (3)
Sex ratio among normal sibs of persons with Turner's syndrome (1974) (3)
138: XY females with camptomelic dwarfism – lack of male gonadal differentiation coupled with abnormal cartilage (1976) (3)
Diagnostic transcervical chorionic biopsles in first trimester pregnancies (1984) (3)
Stability of abnormal karyotypes in cell culture. (1969) (3)
Workshop on collaborative studies in prenatal diagnosis of chromosome disease. (1982) (2)
Human cytogenetic registers. A description of nine systems together with some recommendations. (1977) (2)
16. Male Fenotype Without Demonstrable Y‐chromosome (1965) (2)
Identification of different translocations in man by fluorescence analysis Robertsonian quinacrine mustard (1971) (2)
Human cytogenetic registers. A description of nine systems together with some recommendations. (1977) (2)
Methodological aspects on the estimation of genetic effects of environmental agents in man. (1974) (2)
[The retinoblastoma team at Karolinska hospital]. (1979) (2)
Identification of human chromosomes by fluorescence techniques. (1972) (1)
Nobel Assembly (1983) (1)
Iron malabsorption and hypochromic anemia in a case of Turner's syndrome (1978) (1)
[Prenatal diagnosis of genetic diseases]. (1972) (1)
ENDOREDUPLICATION OF CHROMOSOMES (1964) (1)
[Congenital malformations in children of elderly mothers (aged 42 & over)]. (1959) (1)
Testicular germinal dysgenesis (male Turner's syndrome). Report of a case with chromosomal studies and review of the literature. (1961) (1)
STABILITY OF ABNORMAL KARYOTYPES IN CELL CULTURE1 (2009) (0)
Corrigenda (1972) (0)
[What possibilities do we have for measuring the genetic effects of exogen agents in man?]. (1972) (0)
Subject Index Vol. 19, 1977 (1977) (0)
Re: "Epidemiology of chromosome abnormalities in man". (1978) (0)
[The environmental registry of cancer's data are unsatisfactory for analysis of connection between the parent's occupation and the child's cancer]. (1982) (0)
[Fetal diagnosis during the first trimester by transcervical aspiration of chorionic villi]. (1983) (0)
the Maternal Chromosome Number 22 Clonal Origin of the Philadelphia Chromosome From Either the Paternal or (2011) (0)
[Santiago Ramon y Cajal and neurobiology]. (2001) (0)
Contents, Vol. 19, 1977 (1977) (0)
Standard Outline for Each Nation (2.1–2.19) (1989) (0)
[Genetic counseling in nursing - ethics and psychological aspects]. (1975) (0)
[Endogenous hearing impairments]. (1971) (0)
[Genetics in medical studies]. (1971) (0)
RELEVANCE OF MEIOTIC STUDIES IN HUMAN CHROMOSOME IDENTIFICATION (1968) (0)
[The man behind the syndrome: Henry Turner. He established a relationship between short stature and ovarian dysfunction in girls]. (1983) (0)
[More geneticists needed in our district hospitals]. (1967) (0)
[Cytogenetic and clinical studies in children whose parents have been treated with iodine isotopes]. (1971) (0)
[Philadelphia chromosomes]. (1966) (0)
[Antenatal detection of genetic diseases by study of the amniotic fluid]. (1971) (0)
[Can environmental poisoning produce genetic injuries in man?]. (1971) (0)
Origin of the Philadelphia chromosome. Tracing of chromosome 22 to parents of patients with chronic myelocytic leukemia. (1973) (0)
Late Effects of Chemotherapy (1980) (0)
[Genetic counseling in the medical services--ethical and psychological aspects]. (1975) (0)
[University hospital--an academy. Concentrating research resources]. (1993) (0)
Genetic aspects of psoriasis: mode of inheritance and action of PUVA on DNA. (1981) (0)
[Research must be profiled within a new health care structure. Interview by Eva Oldinger]. (1996) (0)
H'-THYMIDINE UPTAKE BY A RING X CHROMOSOME IN A HUMAN FEMALE BY JANET ROWLEY, SYLFEST MULDAL, (0)
[Can synthetic progestogenic steroids during early pregnancy cause hypospadias in the male fetus?]. (1971) (0)
Changes in the incidence of Down syndrome in Sweden during 1968-1982. (1986) (0)

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Jan E. Lindsten's Published Works

Published Works

What Schools Are Affiliated With Jan E. Lindsten?

Jan E. Lindsten's AcademicInfluence.com Rankings