M. L. G. Ern Fellous

M. L. G. Ern Fellous's AcademicInfluence.com Rankings

Biology

#10868

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#14227

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Evolutionary Biology

#246

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#268

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Genetics

#1167

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#1266

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Molecular Biology

#1622

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#1650

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M. L. G. Ern Fellous'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

Genetic evidence equating SRY and the testis-determining factor (1990) (915)
Donor splice-site mutations in WT1 are responsible for Frasier syndrome (1997) (680)
A protein tyrosine kinase in the interferon α β signaling pathway (1992) (634)
Preferential effect of γ interferon on the synthesis of HLA antigens and their mRNAs in human cells (1982) (361)
A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development. (1993) (356)
Linkage and association of the glutamate receptor 6 gene with autism (2002) (319)
A 11.7-kb deletion triggers intersexuality and polledness in goats (2001) (314)
Genetic evidence that ZFY is not the testis-determining factor (1989) (298)
Evolution and expression of FOXL2 (2002) (275)
TNF stimulates expression of mouse MHC class I genes by inducing an NF kappa B‐like enhancer binding activity which displaces constitutive factors. (1989) (264)
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. (2006) (255)
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation. (2001) (251)
A glycolipid antigen associated with Burkitt lymphoma defined by a monoclonal antibody. (1983) (231)
Mutant cohesin in premature ovarian failure. (2014) (229)
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. (2003) (226)
Interferon-dependent induction of mRNA for the major histocompatibility antigens in human fibroblasts and lymphoblastoid cells. (1982) (218)
A protein tyrosine kinase in the interferon alpha/beta signaling pathway. (1992) (209)
Interferon-α-dependent Activation of Tyk2 Requires Phosphorylation of Positive Regulatory Tyrosines by Another Kinase* (1996) (193)
Interferon response sequence potentiates activity of an enhancer in the promoter region of a mouse H–2 gene (1986) (185)
An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation. (2004) (183)
The effect of gamma-interferon on MHC antigens. (1984) (180)
CATSPER2, a human autosomal nonsyndromic male infertility gene (2003) (175)
Human XX males with Y single-copy DNA fragments (1984) (175)
Characterization of a human ovarian teratocarcinoma‐derived cell line (1980) (164)
Monoclonal antibody against a Burkitt lymphoma-associated antigen. (1981) (160)
A view of the neolithic demic diffusion in Europe through two Y chromosome-specific markers. (1996) (160)
The protein encoded by a murine male germ cell-specific transcript is a putative ATP-dependent RNA helicase (1989) (158)
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distance. (1985) (157)
Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines (1978) (154)
Isolation of a human teratoma cell line which expresses F9 antigen (1977) (150)
Probable Haploid Expression of HL-A Antigens on Human Spermatozoon (1970) (141)
Disruption of the principal, progesterone-activated sperm Ca2+ channel in a CatSper2-deficient infertile patient (2013) (141)
Small deletions of the short arm of the Y chromosome in 46,XY females. (1986) (140)
Sex chromosome mosaicism in males carrying Y chromosome long arm deletions. (2000) (136)
Enhanced expression of HLA antigens and β2‐microglobulin on interferon‐treated human lymphoid cells (1979) (135)
The amino-terminal region of Tyk2 sustains the level of interferon alpha receptor 1, a component of the interferon alpha/beta receptor. (1997) (132)
Structure, evolution and expression of the FOXL2 transcription unit (2003) (129)
Genetic male infertility and mutation of CATSPER ion channels (2010) (128)
Aetiological diagnosis of male sex ambiguity: a collaborative study (2001) (123)
Report of the committee on the genetic constitution of the X and Y chromosomes. (1987) (120)
The human Y chromosome: the biological role of a “functional wasteland” (2001) (119)
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. (2005) (118)
Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics (2007) (116)
Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA‐sequences (1994) (115)
The beta2‐microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon. (1983) (111)
Novel paralogy relations among human chromosomes support a link between the phylogeny of doublesex-related genes and the evolution of sex determination. (2002) (110)
Genetic investigation of four meiotic genes in women with premature ovarian failure. (2008) (109)
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene. (1997) (106)
Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1. (1997) (106)
A high frequency of Y chromosome deletions in males with nonidiopathic infertility. (1999) (105)
FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD) (2008) (105)
Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype (1997) (104)
True hermaphroditism: genetic variants and clinical management. (1994) (102)
Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice (2009) (97)
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation (2004) (96)
The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain. (2000) (95)
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis. (2000) (92)
Single-copy DNA sequences specific for the human Y chromosome (1983) (90)
Specific Contribution of Tyk2 JH Regions to the Binding and the Expression of the Interferon α/β Receptor Component IFNAR1* (1998) (88)
Molecular genetics of sex determination. (2002) (86)
Isolation of a B-cell-specific promoter for the human class II transactivator (1997) (85)
Differential regulation of HLA‐DR mRNAs and cell surface antigens by interferon. (1983) (85)
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor (1999) (85)
Familial case with sequence variant in the testis-determining region associated with two sex phenotypes. (1992) (81)
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development. (2007) (77)
Population Structure in the Mediterranean Basin: A Y Chromosome Perspective (2006) (76)
Sex determination and the Y chromosome. (1999) (76)
Testis determination in mammals: more questions than answers (2001) (75)
Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism. (2000) (74)
Extensive sequence homologies between Y and other human chromosomes. (1984) (73)
True hermaphroditism: clinical aspects and molecular studies in 16 cases. (1997) (73)
Recent advances in the study of genes involved in non-syndromic premature ovarian failure (2008) (73)
Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) (2010) (72)
Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome. (1998) (71)
The mutations and potential targets of the forkhead transcription factor FOXL2 (2008) (71)
A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing. (2016) (71)
Regulation of HLA-DR gene by IFN-gamma. Transcriptional and post-transcriptional control. (1988) (71)
A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome. (1996) (70)
Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in children. (2007) (69)
FOXL2 mutation screening in a large panel of POF patients and XX males (2002) (68)
XY sex reversal associated with a nonsense mutation in SRY. (1992) (67)
Foxl2 gene and the development of the ovary: a story about goat, mouse, fish and woman. (2005) (66)
The human SRY protein is present in fetal and adult Sertoli cells and germ cells. (1999) (66)
Y chromosome DNA polymorphisms in human populations: differences between Caucasoids and Africans detected by 49a and 49f probes (1990) (66)
Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination. (1996) (66)
Interferon and major histocompatibility complex genes: a model to analyse eukaryotic gene regulation? (1986) (65)
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 (2009) (65)
Sexing bovine embryos using Y chromosome specific DNA probe (1987) (65)
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles. (2008) (64)
A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus. (1982) (63)
The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target site. (2005) (62)
The common, Near‐Eastern origin of Ashkenazi and Sephardi Jews supported by Y‐chromosome similarity (1993) (60)
Interferon α Inhibits a Src-mediated Pathway Necessary for Shigella-induced Cytoskeletal Rearrangements in Epithelial Cells (1998) (58)
Cloacal exstrophy in an infant with 9q34.1‐qter deletion resulting from a de novo unbalanced translocation between chromosome 9q and Yq (2004) (58)
A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY (1992) (57)
Absence of allogeneic restriction in human T-cell-mediated cytotoxicity to Epstein-Barr virus-infected target cells. Demonstration of an HLA- linked control at the effector level (1979) (56)
Activation of the protein tyrosine kinase tyk2 by interferon alpha/beta. (1994) (55)
A non‐sense MCM9 mutation in a familial case of primary ovarian insufficiency (2016) (54)
The human doublesex-related gene, DMRT2, is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript. (2000) (53)
Developmental expression of an early embryonic antigen common to mouse spermatozoa and cleavage embryos, and to human spermatozoa: its expression during spermatogenesis. (1976) (53)
The genetic basis of murine and human sex determination: a review (1995) (51)
Y chromosome haplogroups in autistic subjects (2002) (51)
A possible common origin of “Y-negative” human XX males and XX true hermaphrodites (1990) (51)
Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome (2008) (51)
Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor. (1993) (50)
Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. (1993) (49)
Similar location of an early embryonic antigen on mouse and human spermatozoa. (1974) (49)
Molecular analysis of 60,XX pseudohermaphrodite polled goats for the presence of SRY and ZFY genes. (1994) (47)
Human virus-infected target cells lacking HLA antigens resist specific T-lymphocyte cytolysis (1977) (47)
Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis. (2003) (46)
North African Jewish and non-Jewish populations form distinctive, orthogonal clusters (2012) (45)
SRY-negative XX fetus with complete male phenotype (1994) (45)
Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses (2002) (44)
HLA monoclonal antibody registry: a proposal. (2008) (44)
Studies on the Biosynthetic Pathway of Human P Erythrocyte Antigens Using Somatic Cells in Culture (1974) (43)
Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene. (1994) (41)
Genetic mapping of the autosomal region involved in XX sex-reversal and horn development in goats (1996) (41)
Induction of the expression of HLA class I antigens on K562 by interferons and sodium butyrate. (1985) (41)
Variations of the Expression of HL-A Antigens on Human Diploid Fibroblasts in vitro (1971) (40)
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation. (2005) (40)
High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23. (1999) (40)
) FOXL 2 and BPES : Mutational hotspots , phenotypic variability , and revision of the genotype-phenotype correlation (2003) (39)
Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in children. (2008) (37)
Familial occurrence of the IMAGe association: additional clinical variants and a proposed mode of inheritance. (2005) (37)
Sense and antisense Foxl2 transcripts in mouse. (2005) (36)
Direct hybridization of sorted human chromosomes: localization of the Y chromosome on the flow karyotype. (1983) (36)
Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis. (2001) (36)
Characterization of a putative type IV aminophospholipid transporter P-type ATPase (2003) (35)
Genetic analysis of 38XX males with genital ambiguities and true hermaphrodites in pigs. (2009) (34)
Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution. (2001) (34)
ABSENCE OF A SEROLOGICALLY DETECTABLE ASSOCIATION OF MURINE β2‐MICROGLOBULIN WITH THE EMBRYONIC F9 ANTIGEN (1976) (34)
A monoclonal antibody with anti‐burkitt lymphoma specificity. I. Analysis of human haematopoietic and lymphoid cell lines (1982) (32)
Recovery of Female Fertility After Chemotherapy, Irradiation, and Bone Marrow Allograft: Further Evidence Against Massive Oocyte Regeneration by Bone Marrow‐Derived Germline Stem Cells (2007) (32)
Studies of human alloantigens on man‐mouse hybrids: possible syntheny between hl‐a and p systems (1973) (31)
HLA class I genes integrated into murine cells are inducible by interferon (1983) (31)
Characterization and sequence of the 5' flanking region of the human testis-determining factor SRY (1992) (31)
Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure (2012) (30)
THE TIME OF APPEARANCE OF Ia ANTIGENS DURING SPERMATOGENESIS IN THE MOUSE (1976) (29)
GermOnline, a cross-species community knowledgebase on germ cell differentiation (2004) (28)
Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene (1998) (28)
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction. (2005) (28)
Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues. (2001) (28)
Contribution of domestic animals to the identification of new genes involved in sex determination. (2001) (26)
Genetic mapping of the polled/intersex locus (PIS) in goats (1997) (26)
FOXO3a variants in patients with premature ovarian failure (2008) (26)
A molecular approach to the study of the human Y chromosome and anomalies of sex determination in man. (1986) (26)
Regulation of histocompatibility antigensby interferon (1985) (25)
Sex-Determining Genes (1997) (24)
Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography. (2009) (24)
A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure (2009) (23)
Control of sex determination in animals. (1993) (23)
The expression of human beta2 microglobulin on human spermatozoa (1976) (23)
Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata. (1995) (23)
GermOnline, a new cross-species community annotation database on germ-line development and gametogenesis (2003) (23)
A study of the coregulation and tissue specificity of XG and MIC2 gene expression in eukaryotic cells. (2000) (23)
Conservation of Y chromosome-specific sequences immediately 5' to the testis determining gene in primates. (1997) (23)
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency. (2011) (22)
Reactivity of Human Lymphoid and Lymphoblastoid Cells with Peanut Agglutinin: Detection of a Blood Cell Subset which Lacks Detectable Membrane HLA (1980) (22)
Phenotype and surface antigens of mouse teratocarcinoma × fibroblast cell hybrids (1979) (22)
NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system (2001) (22)
Identification of a viral antigen recognized by H-2-restricted cytolytic T lymphocytes on a murine leukemia virus-induced tumor. (1983) (21)
CHARACTERIZATION OF HUMAN TERATOMA CELL LINES FOR THEIR IN VITRO DEVELOPMENTAL PROPERTIES AND EXPRESSION OF EMBRYONIC AND MAJOR HISTOCOMPATIBILITY LOCUS‐ASSOCIATED ANTIGENS (1981) (21)
Regional mapping of the HLA on the short arm of chromosome 6 (1979) (21)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities. (1996) (20)
Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe (1987) (19)
Induction of HLA expression in Daudi cells after cell fusion (1977) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms? (2010) (19)
SRY protein is expressed in ovotestis and streak gonads from human sex-reversal (2001) (19)
[Human infertility: meiotic genes as potential candidates]. (2002) (18)
Transformation of LMTK- cells with purified HLA class I gene. VI. Serological characterization of HLA-B7 and AW24 molecules. (1984) (18)
Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia. (2001) (18)
A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome. (2017) (17)
Expression of the Xga antigen on Cells in culture and its segregation in somatic cell hybrids (1974) (17)
Gonad development in Drash and Frasier syndromes depends on WT1 mutations. (2003) (17)
Testis-specific transcripts detected by a human Y-DNA-derived probe. (1987) (17)
Persistence of Mtillerian Remnants in Complete Androgen Insensitivity Syndrome (2002) (17)
Male-specific protein (MSP): A new gene linked to sexual behavior and aggressiveness of tilapia males (2008) (16)
Studies on the Biosynthetic Pathway of Human P Erythrocyte Antigen using Genetic Complementation Tests between Fibroblasts from Rare p and Pk Phenotype Donors (1977) (16)
Effects of H--Y antigen on morphologic and endocrine differentiation of gonads in mammals. (1982) (16)
Y chromosome microsatellite variation in three populations of Jerba Island (Tunisia) (2001) (16)
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans (2016) (16)
Molecular aspects of female and male gonadal development in mammals. (2004) (16)
Dysgerminoma in a pure 45,X Turner syndrome: report of a case and review of the literature. (1994) (16)
The transcription factor FOXL2 in ovarian function and dysfunction. (2010) (15)
[Juvenile granulosa-cell tumor: clinical and molecular expression]. (2009) (14)
Uncoordinated HLA-D Gene Expression in a RFXANK-Defective Patient with MHC Class II Deficiency1 (2001) (14)
Transmission of an unbalanced (Y;1) translocation in Brittany, France (2002) (14)
Cytogenetic study of a European Burkitt's lymphoma cell line. (1979) (14)
CITED2 mutations potentially cause idiopathic premature ovarian failure. (2012) (14)
Partial defects in transcriptional activity of two novel DAX‐1 mutations in childhood‐onset adrenal hypoplasia congenita (2006) (13)
Presence of an abnormal β2-microglobulin mRNA in Daudi cells: Induction by interferon (2004) (13)
The expression and relation of HLA, β2 ‐microglobulin and receptor for marmoset red blood cells on man/mouse and man/Chinese hamster hybrid cells (1977) (12)
Distribution of Y chromosome lineages in Jerba island population. (2005) (12)
The p12f2/TaqI Y-specific polymorphism in three groups of Italians and in a sample of Senegalese. (1987) (12)
A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1 (1990) (12)
Agar human T cell colony growth promoted by a B + null cell-derived lymphokine distinct from IL 2. (1985) (12)
Receptors for IgM on Human Lymphoblastoid B and T Cell Lines (1979) (12)
Y chromosome microsatellite variation in three populations of Jerba Island (Tunisia). (2001) (12)
Differential expression of MHC class II isotype chains. (1999) (12)
Investigation of the ZFY gene in XX true hermaphroditism and Swyer syndrome (1990) (11)
Human chromosome 16 encodes a factor involved in induction of class II major histocompatibility antigens by interferon gamma. (1991) (11)
PRESENCE OF SLA AND Ia‐LIKE ANTIGEN ON BOAR SPERMATOZOA (1978) (11)
The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variability. (1992) (11)
Selective expression of blood group antigens on human teratocarcinoma cell lines. (1981) (10)
Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments (1999) (10)
Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13. (1997) (10)
MHC class II-deficient tumor cell lines with a defective expression of the class II transactivator. (2002) (10)
Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24 (1989) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome (1998) (9)
Genetic Counseling for the Orthodox Jewish Couple Undergoing Preimplantation Genetic Diagnosis (2012) (9)
Qualitative differences in effects of recombinant α−, β− and γ-interferons on human peripheral blood leukocytes in vitro (1986) (9)
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome. (1975) (8)
Characterization of human IFN-γ response using somatic cell hybrids of hematopoietic and nonhematopoietic origin (1989) (8)
CLINICAL, CYTOGENETICAL, HISTOLOGICAL, IMMUNOLOGICAL AND HORMONAL STUDIES IN A CASE OF TRUE HERMAPHRODITISM (1980) (8)
The time of appearance of Ia antigens during spermatogenesis in the mouse. Relationship between Ia antigens and H-2, beta 2 microglobulin and F9 antigens [proceedings]. (1976) (8)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Mutations in the NOG gene are not a common cause of nonsyndromic premature ovarian failure (2007) (8)
Hormonal and molecular genetic findings in 46,XX subjects with sexual ambiguity and testicular differentiation (2005) (8)
Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity? (2014) (8)
The amino-terminal region of Tyk2 sustains the level of interferon a receptor 1, a component of the interferon ayb receptor (1997) (8)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Monoclonal antibodies as a tool for phylogenetic studies of major histocompatibility antigens and β2-microglobulin (2004) (7)
Regulation of histocompatibility antigens by interferon. (1985) (7)
The X chromosome and ovarian function (2003) (7)
We request a serious reconsideration of the recent paper by Seralini et al. alleging tumorigenesis in rats resulting from consumption of corn derived from crops improved through biotechnology (Séralini et al., 2012). (2013) (7)
[Genetic causes of male infertility]. (1999) (6)
The preliminary investigation (protocol) of the malformed fetus or neonate--or--what to do until the pathologist comes. (1979) (6)
Mapping the Xga red blood cell antigen in human-Chinese hamster cell hybrids. The Xg locus is possibly located on the short arm of the X chromosome. (1975) (6)
CIITA B-cell-specific promoter suppression in MHC class II-silenced cell hybrids (1998) (6)
Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion (1995) (6)
ABSORPTION ANALYSIS OF H‐2D AND K ANTIGENS ON SPERMATOZOA (1977) (6)
Transfer of yeast artificial chromosomes into mammalian cells and comparative study of their integrity. (1995) (5)
Association of FOXD 1 variants with adverse pregnancy outcomes in mice and humans (2016) (5)
Sequences homologous to the human y chromosome detected in the female genome (1984) (5)
[Diagnosis of the sex of bovine embryos using molecular biology]. (1990) (5)
Interspecific Chromosome-Wide Transcription Profiles Reveal the Existence of Mammalian-Specific and Species-Specific Chromosome Domains (2004) (5)
A novel mutation 5’ to the HMG box of theSRY gene in a case of Swyer syndrome (1999) (5)
A Y-chromosome portrait of the population of Jerba (Tunisia) to elucidate its complex demographic history (2005) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Identification of signalling components in tyrosine kinase cascades using phosphopeptide affinity chromatography. (1997) (4)
Qualitative differences in effects of recombinant alpha-, beta- and gamma-interferons on human peripheral blood leukocytes in vitro. (1986) (4)
[beta2-Microglobulin in human seminal fluid (author's transl)]. (1978) (4)
Foxl-2 in gonad development and pathology. (2011) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
[Origin and evolution of mammalian sex chromosomes]. (2001) (4)
[Probable linkage between the locus "HLA" and"P"]. (1971) (4)
PERIPHERAL BLOOD T LYMPHOCYTES BEARING DR ANTIGEN AFTER BONE MARROW TRANSPLANTATION (1983) (4)
Are there human analogs of the mouse T locus in central nervous system malformations? (1979) (3)
GENETIC BASIS OF HUMAN SEX DETERMINATION : AN OVERVIEW (1997) (3)
[The analysis of SRY doesn't explain all the pathology of sex determination]. (1991) (3)
[Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes]. (2008) (3)
A quantitative radioimmunoassay for membranous and soluble H-Y antigen typing (2004) (3)
[Chromosome Y and infertility in men]. (2003) (3)
The Study of Human Ia‐Like Specificities Using Antibody Eluates from Human Lymphoblastoid Cell Lines (1977) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
A new Epstein-Barr virus negative Burkitt's lymphoma derived cell-line. I. Analysis of cell surface markers and abnormal expression of HLA antigens. (2008) (3)
The transcription factor FOXL 2 in ovarian function and dysfunction (2009) (3)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
[Male infertility and microdeletions of the Y chromosome]. (2002) (3)
HLA-DR-specific monoclonal antibodies cross-react with several self and nonself non-MHC molecules (2004) (3)
Evidence of a preferential inactivation of the paternally derived X chromosome in a 46,XX true hermaphrodite (2004) (3)
Hermaphroditism pathology. (1999) (2)
Human cells allosensitized in vitro release soluble suppressor factors: presence of at least two distinct factors. (1985) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
Formal genetics of the HL-A region. (1975) (2)
[The Human Genome Project and the genetics of infertility]. (2000) (2)
[Presence of 2 different epitopes on the human beta 2-microglobulin defined by monoclonal antibodies]. (1983) (2)
[A monoclonal antibody, specific for Burkitt's lymphoma, is also a blood group Pk antibody]. (1984) (2)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
A protein from Daudi cell line conditioned medium induces ovarian dysgenesis in Drosophila melanogaster. (1992) (2)
Functional study and detection of HLA-D products on fractionated human bone marrow cells. (2008) (2)
Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis (2004) (2)
INTERFERON-INDUCED PROTEINS: BIOLOGICAL FUNCTIONS AND CLINICAL APPLICATIONS (1982) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Specific contribution of Tyk2 JH regions to the binding and the expression of the interferon alpha/beta receptor component IFNAR1 (2021) (2)
[Production of monoclonal antibodies against HBs (author's transl)]. (1981) (2)
Prenatal identification of a Y‐chromosome deletion by Y‐specific single copy DNA probes (1986) (1)
[Sex determination and differentiation in man: from pathology to genes]. (1997) (1)
[Hermaphroditism pathology]. (2004) (1)
[Y chromosome and spermatogenesis]. (1997) (1)
The recombinant human interferon-gamma receptor is fully functional in a human x murine hybrid containing human chromosome 21. (1991) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
INFLUENCE OF RECOMBINANT INTERLEUKIN‐2 AND α‐ AND γ‐INTERFERONS ON THE INDUCTION OF NOVEL CLASS I ANTIGENS (1990) (1)
Relationship Between Y-Chromosome and H-Y Antigen Expression in Human Spermatozoa (1983) (1)
The RAG cell line defines a new complementation group of MHC class II deficiency (2005) (1)
DNA ANALYSIS OF XX MALES WITH GENITAL ABNORMALITIES COMPARED TO “CLASSICAL” XX MALES (1986) (1)
Genetic analysis of human male infertility (2009) (1)
[Effect of interferon on human cell lines which do not express class I transplantation antigens: K 562 and Daudi. Presence of a pseudo-messenger RNA of beta 2-microglobulin in Daudi cell line]. (1982) (1)
Genome Editing and Dialogic Responsibility: “What's in a Name?” (2015) (1)
Possible relationship between H-Y antigen and female gonadogenesis in the Colorado potato beetle, Leptinotarsa decemlineata (Coleoptera: Chrysomelidae) (1986) (1)
[Isolation of the sex-determining gene in men]. (1992) (1)
Genetic mapping of a male germ cell-expressed gene Tpx-2 to mouse chromosome 17 (2004) (1)
[Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)]. (1980) (1)
Identification of human SRY-interacting factors (2001) (1)
[Genetic control of spermatogenesis: Y chromosome and male infertility]. (1999) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
Dr. Pavol Ivanyi (1930–2005) (2006) (0)
Pillars article: A protein tyrosine kinase in the interferon α/β signaling pathway. Cell. 1992. 70: 313-322. (2011) (0)
[Biological and genetic tests for sexual development disorders]. (2003) (0)
Hormonal and DNA studies in XX males (1984) (0)
Subject Index Vol. 99, 2002 (2003) (0)
[Anonymous sperm donation does not increase the risk for unions between relatives nor the incidence of autosomal recessive diseases due to consanguinity]. (2014) (0)
[46,XX karyotype males, based on a specific case]. (1996) (0)
XX MALES AND AMBIGUOUS GENITALIA: A LINK BETWEEN SRY AND ANDROGEN RECEPTOR (AR) GENE? (1993) (0)
Subject index Vol. 46, 1987 (1987) (0)
P-015: Association of FOXD1 variants with pregnancy failures in mice and humans (2017) (0)
A Monoclonal Antibody Defining a Burkitt Lymphoma Associated Antigen (1982) (0)
[A method of molecular hybridization identification of chromosomes purified with a cell sorter]. (1982) (0)
[Cytotoxicity of human T-lymphocytes sensitized by Epstein-Barr virus. Role of HLA antigens at the surface of target cells infected by the virus]. (1977) (0)
Abstracts from the First Annual Congress for Hybridoma Research. February 15-17, 1982. (1982) (0)
The human genome revolution or evolution? (2001) (0)
Expression and Characterization of Leucocyte Antigens (1984) (0)
Research of a serum anti‐H‐Y antigen in a non inbred strain of rat (1992) (0)
Gene expression pattern NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system (2001) (0)
Dns-tasting, specifically genome for the male of ruminants, their manufacture and use. (1987) (0)
[The genetics of sex]. (1993) (0)
The study of human Aa-like specificities using antibody eluates from human lymphoblastoid cell lines. (1977) (0)
Potential environmental impacts associated with large-scale herbicide-tolerant GM oilseed rape crops: Scientific opinion released by the Biomolecular Engineering Commission (CGB) on February 13, 2004 (2004) (0)
Bibliography of Ulrich Wolf (2001) (0)
[H-Y antigen and sexual dysgenesis in man]. (1981) (0)
TÉRATOCARCINOMES MURINS, LOCUS T ET LIGNÉE GERMINALE (1975) (0)
[Genetic factor of sex determination]. (1991) (0)
Surface markers on mouse cells transformed after exposure to HeLa chromosomes are Mycoplasma membrane proteins. (1982) (0)
[Spina bifida: an equivalent mutation in man of the mouse T locus?]. (1985) (0)
A NovelMutation inthePutative DNA Helicase XH2 IsResponsible forMale-to-Female SexReversal Associated withan Atypical Formof theATR-XSyndrome (1996) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Citation Elements in order: Document Example: (2005) (0)
Abnormal ovarian morphogenesis in Drosophila melanogaster after injection of embryos with conditioned media from the Daudi cell line (1988) (0)
[Immunological characterization and genetic control of the H-Y antigen]. (1983) (0)
[Linkage between the HL-A histocompatibility system and the thymidine kinase activity in a human-mouse hybrid]. (1972) (0)
Table S3 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans (2016) (0)
Contents Vol. 91, 2000 (2001) (0)
[Male XX syndrome: contribution of the caprine and porcine models]. (1996) (0)
Measuring an open and responsible culture discussion (2013) (0)
A whole-embryo culture system proposed to study mouse sexual determination. (1995) (0)
[XX male syndrome: a study model of the genetic determination of the male sex]. (1986) (0)
[Detection of human antigens on the surface of mouse cells transformed by chromosome transfer]. (1979) (0)
Major histocompatibility antigens and beta2-microglobulin. (1982) (0)
Joint meeting of the British & Irish Associations for Cancer Research. November 28-29, 1985, London. Abstracts. (1986) (0)
UvA-DARE ( Digital Academic Repository ) FOXL 2 and BPES : Mutational hotspots , phenotypic variability , and revision of the genotype-phenotype correlation (2017) (0)
[Correlation between the expression of HL-A and P systems antigens in hybrid human x mouse cells and culture media (HATG, Standard, BUDR). Possible linkage of HL-A and P loci with the thymidine kinase locus]. (1973) (0)
[Search for a correlation between the HL-A antigenic system and viral receptors of 3 enterovirus by means of cell hybridization]. (1974) (0)
Evaluation of new real time PCR system for the quantification of Legionella spp and Legionella pneumophila in water samples iQ-CheckTM Quanti Legionella (2003) (0)
Contents Vol. 99, 2002 (2003) (0)
145 ANALYSIS OF XX MALES AND XX TRUE HEREMAPHRODITES, ARGUMENTS FOR A NON-Y TESTICULAR DETERMINING GENE (1988) (0)
Genetic diseases of the red cell membrane permeability (1999) (0)
[The genetics of sex determination]. (2002) (0)
[Normal male phenotype or hypospadias and female karyotype. XX male syndrome in children and adolescents]. (1985) (0)
A tribute to Donald Pious (1930-1998) (1999) (0)
Table S2 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans (2016) (0)
Influence of recombinant interleukin-2 and alpha- and gamma-interferons on the induction of novel class I antigens. (1990) (0)
New molecular defects in two RFXANK-defective patients with MHC class II deficiency (2001) (0)
Subject Index Vol. 101, 2003 (2003) (0)
MODULATION OF THE FREQUENCY PREFERENCE AND ATTRACTOR STRUCTURE OF PREFRONTAL CORTICAL NEURONS (2002) (0)
Figure S1 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans (2016) (0)
Boy or Girl’s Mendelian Genetics with “Precious” Families (2014) (0)
Cell response to the cloning and expression of adjusting the type I interferon protein (1990) (0)
Between hl-a and p systems. (1973) (0)
Subject Index Vol. 91, 2000 (2000) (0)
[Could male infertility become hereditary?]. (1997) (0)
Subject Index, Vol. 37, 1992 (1992) (0)
Supplementary material from "Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans" (2016) (0)
[An XX male newborn infant. A genetic and endocrinologic study]. (1987) (0)
[Cytopathogenic effect in vitro of human leukemic leukoblasts on fibroblasts in culture. Correlation with the stimulating effect in vitro of leukoblasts on autologous lymphocytes]. (1971) (0)
sY116, a human Y-linked polymorphic STS (2000) (0)
[Genetic, biochemical and functional study of the H-Y antigen in man]. (1980) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Contents Vol. 101, 2003 (2003) (0)
Novel insights in genotype-phenotype correlations in BPES through in-depth FOXL2 mutation analysis (2002) (0)
References to the committee reports (1975) (0)
Boy or Girl’s Mendelian Genetics with “Precious” Families (2014) (0)
The amino-terminal region of Tyk2 sustains the level of interferon (cid:97) receptor 1, a component of the interferon (cid:97) (cid:121) (cid:98) receptor (1997) (0)

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