Sets of linked genetic markers for human chromosomesWHITE, R; LALOUEL, J.-M.Annual review of genetics. 1988, Vol 22, pp 259-279, issn 0066-4197Article

MicroVNTR (CTTT)_n at the apo C-III locusHATA, A; LALOUEL, J.-M.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5098Article

Investigation of genetic linkage in human familiesWHITE, R; LALOUEL, J.-M.Advances in human genetics. 1987, Vol 16, pp 121-228, issn 0065-275XArticle

Detection of linkage between a quantitative trait and a marker locus by the lod score method: sample size and sampling considerationsDEMENAIS, F; LATHROP, G. M; LALOUEL, J. M et al.Annals of human genetics. 1988, Vol 52, Num 3, pp 237-246, issn 0003-4800Article

Robustness and power of the unified model in the analysis of quantitative measurementsDEMENAIS, F; LATHROP, M; LALOUEL, J. M et al.American journal of human genetics. 1986, Vol 38, Num 2, pp 228-234, issn 0002-9297Article

Linkage disequilibrium between DNA markers at the low-density lipoprotein receptor geneHEGELE, R. A; PLAETKE, R; LALOUEL, J.-M et al.Genetic epidemiology. 1990, Vol 7, Num 1, pp 69-81, issn 0741-0395, 13 p.Article

Efficient computations in multilocus linkage analysisLATHROP, G. M; LALOUEL, J.-M.American journal of human genetics. 1988, Vol 42, Num 3, pp 498-505, issn 0002-9297Article

Idiopathic hemochromatosis: significance and implications of linkage and association to HLALALOUEL, J.-M; JORDE, L. B.Annals of the New York Academy of Sciences. 1988, Vol 526, pp 34-46, issn 0077-8923Conference Paper

Easy calculations of lod scores and genetic risks on small computersLATHROP, G. M; LALOUEL, J. M.American journal of human genetics. 1984, Vol 36, Num 2, pp 460-465, issn 0002-9297Article

Path analysis of family resemblance and gene-environment interactionLATHROPE, G. M; LALOUEL, J. M; JACQUARD, A et al.Biometrics. 1984, Vol 40, Num 3, pp 611-625, issn 0006-341XArticle

Angiotensinogen Thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first-trimester deciduaMORGAN, T; CRAVEN, C; LALOUEL, J.-M et al.American journal of obstetrics and gynecology. 1999, Vol 180, Num 1, pp 95-102, issn 0002-9378, 1Article

Genetic markers in human hypertensionLALOUEL, J.-M.American journal of hypertension. 1991, Vol 4, Num 11, pp 594S-597S, issn 0895-7061Conference Paper

Lipoprotein lipase : molecular model based on the pancreatic lipase X-ray structure : consequences for heparin binding and catalysisVAN TILBEURGH, H; ROUSSEL, A; LALOUEL, J.-M et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 6, pp 4626-4633, issn 0021-9258Article

Strategies for multilocus linkage analysis in humansLATHROP, G. M; LALOUEL, J. M; JULIER, C et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 11, pp 3443-3446, issn 0273-1134Article

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation : identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase geneHATA, A; ROBERTSON, M; EMI, M et al.Nucleic acids research. 1990, Vol 18, Num 18, pp 5407-5411, issn 0305-1048, 5 p.Article

Combined linkage and segregation analysis using regressive modelsBONNEY, G. E; LATHROP, G. M; LALOUEL, J.-M et al.American journal of human genetics. 1988, Vol 43, Num 1, pp 29-37, issn 0002-9297Article

Construction of human linkage maps: likelihood calculations for multilocus linkage analysisLATHROP, G. M; LALOUEL, J. M; WHITE, R. L et al.Genetic epidemiology. 1986, Vol 3, Num 1, pp 39-52, issn 0741-0395Article

Tests of gene order from three-locus linkage dataLATHROP, G. M; CHOTAI, J; OTT, J et al.Annals of human genetics. 1987, Vol 51, Num 3, pp 235-249, issn 0003-4800Article

Multilocus linkage analysis in humans: detection of linkage and estimation of recombinationLATHROP, G. M; LALOUEL, J. M; JULIER, C et al.American journal of human genetics. 1985, Vol 37, Num 3, pp 482-498, issn 0002-9297Article

Elements of a paracrine tubular renin-angiotensin system along the entire nephronROHRWASSER, A; MORGAN, T; TERREROS, D. A et al.Hypertension (Dallas, Tex. 1979). 1999, Vol 34, Num 6, pp 1265-1274, issn 0194-911XArticle

Exclusion of the Na⁺-H⁺ antiporter as a candidate gene in human essential hypertensionLIFTON, R. P; HUNT, S. C; WILLIAMS, R. R et al.Hypertension (Dallas, Tex. 1979). 1991, Vol 17, Num 1, pp 8-14, issn 0194-911X, 7 p.Article

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2 : evidence for a gene-gene interactionHOPKINS, P. N; WU, L. L; SCHUMACHER, M. C et al.Arteriosclerosis and thrombosis. 1991, Vol 11, Num 5, pp 1137-1146Article

Isolation and mapping of a polymorphic DNA sequence (HB118P1)on chromosome 11 [D11S147]JULIER, C; NAKAMURA, Y; LATHROP, G. M et al.Nucleic acids research. 1989, Vol 17, Num 22, issn 0305-1048, 9510 [1 p.]Article

Isolation and mapping of a polymorphic DNA sequence (pCJ52-75M1) on chromosome II [D11S385]JULIER, C; NAKAMURA, Y; LATHROP, G. M et al.Nucleic acids research. 1989, Vol 17, Num 22, issn 0305-1048, 9505 [1 p.]Article

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