James L. German
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James L. Germanbiology Degrees
Biology
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Cell Biology
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Genetics
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Molecular Biology
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Biology
James L. German's Degrees
- PhD Molecular Biology Stanford University
Why Is James L. German Influential?
(Suggest an Edit or Addition)James L. German's Published Works
Number of citations in a given year to any of this author's works
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 Bloom's syndrome gene product is homologous to RecQ helicases (1995) (1354)
- A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. (1974) (892)
- Bloom Syndrome: A Mendelian Prototype of Somatic Mutational Disease (1993) (538)
- Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. (1969) (438)
- Bloom's syndrome (1992) (322)
- Bloom's syndrome. XX. The first 100 cancers. (1997) (275)
- Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients. (1969) (240)
- Enhanced Tumor Formation in Mice Heterozygous for Blm Mutation (2002) (214)
- A retarded rate of DNA chain growth in Bloom's syndrome. (1975) (200)
- Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. (1989) (187)
- Cytological Evidence for Crossing-Over in vitro in Human Lymphoid Cells (1964) (187)
- THE PATTERN OF DNA SYNTHESIS IN THE CHROMOSOMES OF HUMAN BLOOD CELLS (1964) (177)
- Molecular genetics of Bloom's syndrome. (1996) (176)
- Syndrome‐causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry (2007) (174)
- Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells. (1995) (141)
- Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes. (1977) (140)
- Altered DNA ligase I activity in Bloom's syndrome cells (1987) (132)
- Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth. (1966) (122)
- III. DNA SYNTHESIS IN HUMAN CHROMOSOMES (1962) (119)
- Bloom's Syndrome. XII. Report from the Registry for 1987 (1989) (113)
- An abnormal profile of DNA replication intermediates in Bloom's syndrome. (1990) (109)
- The Roberts syndrome (1974) (106)
- A previously unrecognized X-linked syndrome of dysmorphia. (1975) (105)
- Bloom's syndrome and Fanconi's anemia: Demonstration of two distinctive patterns of chromosome disruption and rearrangement (1974) (103)
- Roberts' syndrome.I. Cytological evidence for a disturbance in chromatid pairing (1979) (103)
- MONGOLISM BY TERTIARY TRISOMY (1975) (96)
- Bloom's syndrome. V. Surveillance for cancer in affected families (1977) (94)
- Bloom's syndrome protein, BLM, colocalizes with replication protein A in meiotic prophase nuclei of mammalian spermatocytes. (1999) (94)
- Evidence for chromosome instability in vivo in bloom syndrome: Increased numbers of micronuclei in exfoliated cells (2004) (94)
- Bloom's syndrome: evidence for an increased mutation frequency in vivo. (1983) (91)
- Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1. (1994) (85)
- Molecular evidence that homologous recombination occurs in proliferating human somatic cells. (1990) (84)
- Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp (1994) (83)
- Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population. (1998) (81)
- Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development (2015) (78)
- CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME. (1964) (75)
- Genetically determined sex-reversal in 46,XY humans (1978) (74)
- Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder (2004) (72)
- The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry. (1998) (69)
- PBDX is the XG blood group gene (1994) (66)
- Chromosome studies in “preleukemia”. III. myelofibrosis (1976) (64)
- BLM, the Bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins (2001) (64)
- Impaired immune function in patients with xeroderma pigmentosum. (1985) (64)
- Bloom's Syndrome. VII. Progress report for 1978 (1979) (63)
- Abnormal immune responses of Bloom's syndrome lymphocytes in vitro. (1975) (61)
- Mapping Human Autosomes: Evidence Supporting Assignment of Rhesus to the Short Arm of Chromosome No. 1 (1974) (60)
- Evaluation of Short Stature, Carbohydrate Metabolism and Other Endocrinopathies in Bloom’s Syndrome (2006) (60)
- Bloom's syndrome XI. Progress report for 1983 (1984) (58)
- Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. (1977) (57)
- Pseudovaginal perineoscrotal hypospadias (1972) (56)
- Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients. (1989) (54)
- Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal. (1999) (52)
- Abnormalities of human sex chromosomes (1974) (50)
- Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome. (1994) (50)
- Macrophage Apoptosis by Anthrax Lethal Factor Through p 38 MAP Kinase Inhibition (2002) (47)
- Bloom's syndrome. XIV. The disorder in Japan (1989) (47)
- Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations. (1984) (45)
- Cytogenetic evidence of the intrauterine origin of acute leukemia in monozygotic twins. (1979) (42)
- The human Y chromosome homologue of XG: transcription of a naturally truncated gene. (1995) (42)
- Abnormalities of human sex chromosomes. V. A unifying concept in relation to the gonadal dysgeneses (1970) (40)
- Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum. (1978) (37)
- Mapping Human Autosomes: Assignment of the MN Locus to a Specific Segment in the Long Arm of Chromosome No. 2 (1973) (37)
- Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest. (1979) (36)
- In vitro labelling of human meiotic chromosomes with H3-thymidine. (2009) (36)
- A test for Fanconi's anemia. (1987) (35)
- Human chromosomal deletion: two patients with the 4p- syndrome. (1970) (34)
- Familial predisposition to cancer and age at onset of disease in randomly selected cancer patients. (1983) (32)
- Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locus. (1992) (30)
- Xeroderma pigmentosum patients from Egypt: II. Preliminary correlations of epidemiology, clinical symptoms and molecular biology. (1981) (30)
- AUTORADIOGRAPHIC STUDIES OF HUMAN CHROMOSOMES. I. A REVIEW. (1969) (30)
- Long‐term study of the immunodeficiency of Bloom's syndrome (1992) (29)
- Genetically Determined Sex‐Reversal in 46, XY Humans (1979) (29)
- Testicular feminization in monozygotic twins with 47 chromosomes (XXY). (1966) (29)
- Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity (1996) (27)
- IDENTIFICATION AND CHARACTERIZATION OF HUMAN CHROMOSOMES BY DNA REPLICATION SEQUENCE (1964) (25)
- Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1. (1996) (24)
- Sister chromatid exchange in cells metabolically coupled to Bloom's syndrome cells (1980) (24)
- Oncogenic Implications of Chromosomal Instability (1973) (24)
- Sensitivity of Bloom's syndrome lymphocytes to ethyl methanesulfonate (2004) (23)
- Chronic renal disease, myotonic dystrophy, and gonadoblastoma in XY gonadal dysgenesis (1982) (23)
- Analysis of Sister‐Chromatid Exchanges (1994) (23)
- THE cis AB PHENOTYPE IN THREE GENERATIONS OF ONE FAMILY: SEROLOGICAL, ENZYMATIC AND CYTOGENETIC STUDIES (1978) (22)
- Bloom's syndrome and EM9 cells in BrdU-containing medium exhibit similarly elevated frequencies of sister chromatid exchange but dissimilar amounts of cellular proliferation and chromosome disruption (2004) (22)
- Familial urinary tract anomalies. (1970) (22)
- Gonadal dimorphism explained as a dosage effect of a locus on the sex chromosomes, the gonad-differentiation locus (GDL). (1988) (22)
- Roberts's syndrome (1981) (22)
- Bloom Syndrome in Sibs: First Reports of Hepatocellular Carcinoma and Wilms Tumor with Documented Anaplasia and Nephrogenic Rests (2001) (22)
- Males with a uterus and fallopian tubes, a rare disorder of sexual development. (1971) (22)
- Bloom's syndrome: DNA replication in cultured fibroblasts and lymphocytes (1977) (21)
- SYNTHESIS OF DEOXYRIBONUCLEIC ACID DURING INTERPHASE (1962) (20)
- Chromosomal breakage in human spermatozoa, a heterozygous effect of the Bloom syndrome mutation. (1994) (19)
- A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene (1998) (18)
- Letter: Mongolism by tertiary trisomy. (1975) (17)
- Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs. (1971) (16)
- Autoradiographic studies of human chromosomes (1969) (16)
- Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization. (1993) (14)
- The chromosome-breakage syndromes: rare disorders that provide models for studying somatic mutation. (1990) (14)
- Different mutations are responsible for the elevated sister-chromatid exchange frequencies characteristic of Bloom's syndrome and hamster EM9 cells. (1987) (14)
- A marrow chromosomal abnormality preceding clinical leukemia in Down's syndrome. (1967) (14)
- Abnormal Y chromosomes and monosomy 45,X: a concept derived from the study of three patients. (1971) (13)
- Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam. (1973) (13)
- The syndrome of congenital telangiectatic erythema and stunted growth. (1971) (13)
- Increased amounts of hybrid (heavy/heavy) DNA in Bloom's syndrome fibroblasts. (1978) (12)
- Bilateral anorchia: discordance in monozygotic twins. (1971) (12)
- DNA REPAIR DEFECTS AND HUMAN DISEASE (1978) (12)
- Triple autosomal trisomy in a pregnancy at risk for Bloom's syndrome. (1991) (10)
- Bloom's syndrome (1972) (10)
- Sclerosing hyaline necrosis of the liver in Bloom syndrome. (2009) (9)
- Autoradiographic studies of human chromosomes. II. Data concerning the position of the MN locus. (1969) (9)
- Autoradiographic studies of human chromosomes (2004) (8)
- [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)]. (1970) (8)
- Testicular feminisation and inguinal hernia. (1973) (8)
- De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation. (1976) (8)
- Analysis of a BrdU-sensitive site in the cactus mouse (Peromyscus eremicus): chromosomal breakage and sister-chromatid exchange (2004) (8)
- Studying human chromosomes today. (1970) (8)
- The Aarskog-Scott syndrome in four brothers. (1975) (7)
- Ulcerative colitis complicated by dysplasia-adenoma-carcinoma in a man with Bloom's syndrome. (1999) (7)
- Polymorphic chromosomes and gene assignment in man. (1975) (7)
- Bloom's syndrome cells have an abnormal serum growth response. (1983) (6)
- Mutant karyotypes in a culture of cells from a man with xeroderma pigmentosum. (1973) (6)
- Constitutional hyperrecombinability and its consequences. (2004) (5)
- Developmental anomaly resembling the trisomy 18 syndrome. (1969) (5)
- Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits (1974) (5)
- [A short arm deletion of chromosome 13]. (1968) (5)
- Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p. (1971) (5)
- Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditism. (1971) (5)
- Hybridization with human cells corrects the elevated SCE frequency and BrdU hypersensitivity of hamster cell line EM9. (1985) (4)
- Xeroderma pigmentosum, defective DNA repair--and schistosomiasis? (1980) (4)
- XIII. DNA-polymerase activity of cultured lymphoblastoid cells (1986) (4)
- Xeroderma pigmentosum in Egypt. III. ABO blood grouping in 22 affected families (1984) (4)
- The linkage relationships of marker sites on chromosomes no. 2 and 10 (1978) (4)
- The Roberts syndrome. (1974) (4)
- A patient with the Larsen syndrome. (1975) (4)
- Generalized dysmorphia of a similar type in two unrelated babies. (1975) (4)
- Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis. (1971) (3)
- Ambiguous genitalia and mental retardation associated with a translocation 46, XX, t(9; 10) and a deletion in 9q. (1976) (3)
- Absence of Close Linkage Between the Locus for Xg and the Locus for Anhidrotic Ectodermal Dysplasia 1 (1969) (2)
- Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation. (1975) (2)
- Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY. (1974) (2)
- Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. 1969. (2004) (2)
- A bibliography on autoradiographic studies of mammalian chromosomes. (1966) (1)
- Bloom's syndrome (1986) (1)
- DNA synthesis in the meiotic chromosomes of man ‐ A preliminary report (2009) (1)
- Why the lupus problem remains unsolved and I am a human geneticist (2003) (1)
- Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-). (1971) (1)
- Bloom syndrome : An analysis of consanguineous families assigns the locus mutated to chromosome band 15 q 26 . 1 ( homozygosity mapping / nka analysls / genomic instability / chromosome-breakge syndrome ) (1)
- [Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)]. (1970) (1)
- Linkage disequilibrium between BLM, FES, D15S127, and IP15M9 in Ashkenazi Jews with Bloom`s syndrome (BS) (1994) (0)
- Blooms syndrome cells are characterized by high sister chromatid exchange (SCE) and microsatellite repeat instability (1994) (0)
- Table 1. [Molecular Genetic Testing Used in Bloom’s Syndrome]. (2016) (0)
- Table 4. [BLM Pathogenic Allelic Variants Discussed in This GeneReview]. (2016) (0)
- Chromosomes in human cancer. (1974) (0)
- Table 2. [The 207 Malignant Neoplasms Diagnosed in 131 Persons in the Bloom's Syndrome Registry, 1954-2016]. (2016) (0)
- Cytogenetic investigation of the Rhnull phenotype. (1974) (0)
- Autoradiographic studies of human chromosomes. 3. Segregation of the no. 13 chromosomes in one family. (1969) (0)
- Autoradiographic studies of human chromosomes (2004) (0)
- Cytogenetic Investigation of the Rhnull Phenotype 1 (1974) (0)
- Contents Vol. 91, 2000 (2001) (0)
- Aflatoxin-possible factor in liver damage in children. (1974) (0)
- Subject Index Vol. 91, 2000 (2000) (0)
- Bloom's Syndrome XXII. Numerous Founder Mutations Bear Witness to the Persistence of Mutant Alleles in Different Human Populations (2007) (0)
- Subject Index Vol. 20, 1978 (1978) (0)
- Editorial help (2004) (0)
- Human chromosomal deletion: with the 4p-syndrome Two patients (1970) (0)
- Polymorphic chromosomes and gene assignment in man. (1975) (0)
- Identification of the XG blood group gene (1994) (0)
- Autoradiographic studies of human chromosomes. 3. - The arm ratio of the late-replicating X. (1974) (0)
- References to the committee reports (1975) (0)
- Bibliography of Ulrich Wolf (2001) (0)
- R--short-limbed dwarfism. (1974) (0)
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