J.-M. Lalouel

8.7k total citations · 4 hit papers
99 papers, 7.4k citations indexed

About

J.-M. Lalouel is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, J.-M. Lalouel has authored 99 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 37 papers in Genetics and 12 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in J.-M. Lalouel's work include DNA and Nucleic Acid Chemistry (28 papers), Genomic variations and chromosomal abnormalities (19 papers) and DNA Repair Mechanisms (14 papers). J.-M. Lalouel is often cited by papers focused on DNA and Nucleic Acid Chemistry (28 papers), Genomic variations and chromosomal abnormalities (19 papers) and DNA Repair Mechanisms (14 papers). J.-M. Lalouel collaborates with scholars based in United States, France and Belgium. J.-M. Lalouel's co-authors include G.M. Lathrop, Cécile Julier, J Ott, Jürg Ott, M. Leppert, P. O’Connell, R. White, Yusuke Nakamura, Akira Hata and R. White and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

J.-M. Lalouel

99 papers receiving 7.2k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Strategies for multilocus linkage analysis in humans.

1984 2.2k citations G.M. Lathrop, J.-M. Lalouel et al. Proceedings of the National Academy of Sciences profile →
Easy calculations of lod scores and genetic risks on small computers.

1984 1.3k citations G.M. Lathrop, J.-M. Lalouel PubMed profile →
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

1985 1.0k citations G.M. Lathrop, J.-M. Lalouel et al. PubMed profile →
The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

1987 502 citations M. Leppert, P. O’Connell et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J.-M. Lalouel United States	26	3.3k	2.9k	1.1k	917	749	99	7.4k
Lodewijk A. Sandkuijl Netherlands	44	3.9k 1.2×	1.9k 0.7×	765 0.7×	646 0.7×	755 1.0×	94	7.7k
Marcella Devoto Italy	45	2.7k 0.8×	1.8k 0.6×	404 0.4×	563 0.6×	477 0.6×	161	6.6k
G.A.P. Bruns United States	50	6.0k 1.8×	1.9k 0.7×	453 0.4×	319 0.3×	640 0.9×	108	9.7k
Lee S. Weinstein United States	55	5.4k 1.6×	3.7k 1.3×	450 0.4×	1.1k 1.2×	543 0.7×	184	10.4k
Hans Scheffer Netherlands	47	3.7k 1.1×	2.7k 0.9×	349 0.3×	283 0.3×	1.2k 1.6×	191	7.9k
Mona Nemer Canada	57	6.9k 2.1×	1.9k 0.7×	3.2k 3.1×	757 0.8×	493 0.7×	148	10.1k
Adrian Clark United Kingdom	49	3.5k 1.1×	1.7k 0.6×	1.2k 1.1×	3.6k 3.9×	791 1.1×	137	8.2k
Cécile Julier France	44	4.3k 1.3×	6.1k 2.1×	733 0.7×	2.2k 2.4×	632 0.8×	109	11.3k
Carol Nelson‐Williams United States	33	6.8k 2.0×	1.7k 0.6×	913 0.9×	3.2k 3.4×	435 0.6×	56	10.4k
Baoli Yang United States	39	3.9k 1.2×	1.4k 0.5×	428 0.4×	316 0.3×	558 0.7×	84	6.1k

Countries citing papers authored by J.-M. Lalouel

Since Specialization

Citations

This map shows the geographic impact of J.-M. Lalouel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J.-M. Lalouel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.-M. Lalouel more than expected).

Fields of papers citing papers by J.-M. Lalouel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.-M. Lalouel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J.-M. Lalouel. The network helps show where J.-M. Lalouel may publish in the future.

Co-authorship network of co-authors of J.-M. Lalouel

This figure shows the co-authorship network connecting the top 25 collaborators of J.-M. Lalouel. A scholar is included among the top collaborators of J.-M. Lalouel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J.-M. Lalouel. J.-M. Lalouel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gociman, Barbu, Andreas Rohrwasser, Elaine Hillas, et al.. (2008). Response to genetic manipulations of liver angiotensinogen in the physiological range. Journal of Human Genetics. 53(9). 775–788. 4 indexed citations

Gociman, Barbu, Andreas Rohrwasser, Pierre Lantelme, et al.. (2004). Expression of angiotensinogen in proximal tubule as a function of glomerular filtration rate. Kidney International. 65(6). 2153–2160. 26 indexed citations

Borecki, Ingrid B., Michael A. Province, E H Ludwig, et al.. (1997). Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI family heart study. Annals of Epidemiology. 7(1). 13–21. 63 indexed citations

Julier, Cécile, Yusuke Nakamura, G.M. Lathrop, J.-M. Lalouel, & R. White. (1989). Isolation and mapping of a polymorphic DNA sequence (HBI18P1) on chromosome 11 [D11S147]. Nucleic Acids Research. 17(22). 9510–9510. 2 indexed citations

Hunt, Steven C., Lily Wu, Paul N. Hopkins, et al.. (1989). Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension.. Arteriosclerosis An Official Journal of the American Heart Association Inc. 9(3). 335–344. 123 indexed citations

Odelberg, Shannon J., R. Plaetke, L. Ballard, et al.. (1989). Characterization of eight VNTR loci by agarose gel electrophoresis. Genomics. 5(4). 915–924. 73 indexed citations

Nakamura, Yusuke, Melanie Culver, M. Leppert, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]. Nucleic Acids Research. 16(10). 4747–4747. 30 indexed citations

Hoff, M., Yusuke Nakamura, T. Holm, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pHHH208) on chromosome 14 [D14S19]. Nucleic Acids Research. 16(21). 10400–10400. 2 indexed citations

Démenais, Florence, G.M. Lathrop, & J.-M. Lalouel. (1988). Detection of linkage between a quantitative trait and a marker locus by the lod score method: sample size and sampling considerations. Annals of Human Genetics. 52(3). 237–246. 11 indexed citations

10.

Fujimoto, E., Yusuke Nakamura, P. O’Connell, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23]. Nucleic Acids Research. 16(10). 4748–4748. 2 indexed citations

11.

Nakamura, Yusuke, E. Fujimoto, Cindy M. Martin, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence pEFD33.2 on chromosome 12 [D12S14]. Nucleic Acids Research. 16(2). 778–778. 13 indexed citations

12.

Fujimoto, E., Yusuke Nakamura, P. O’Connell, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15 [DlSS44]. Nucleic Acids Research. 16(22). 10942–10942. 2 indexed citations

13.

Nakamura, Yusuke, E. Fujimoto, P. O’Connell, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (cYNA4) on chromosome 2 (D2S50). Nucleic Acids Research. 16(19). 9362–9362. 1 indexed citations

14.

Nakamura, Yusuke, L. Ballard, M. Leppert, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pYNH3) on chromosome X [DXS287]. Nucleic Acids Research. 16(12). 5705–5705. 5 indexed citations

15.

Nakamura, Yusuke, E. Fujimoto, M. Leppert, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFD6) on chromosome 6 (D6S41). Nucleic Acids Research. 16(20). 9888–9888. 1 indexed citations

16.

Nakamura, Yusuke, K. Krapcho, L. Ballard, et al.. (1988). Isolation and mapping of a polymorphic DNA sequence (pKKA12) on chromosome 7 (D7S398). Nucleic Acids Research. 16(20). 9886–9886. 3 indexed citations

17.

Leppert, M., Webster K. Cavenee, T. Holm, et al.. (1986). A primary genetic map of chromosome 13q.. PubMed. 39(4). 425–37. 63 indexed citations

18.

Lathrop, G.M., J.-M. Lalouel, Cécile Julier, & J Ott. (1984). Strategies for multilocus linkage analysis in humans.. Proceedings of the National Academy of Sciences. 81(11). 3443–3446. 2227 indexed citations breakdown →

19.

Morton, N.E. & J.-M. Lalouel. (1981). Resolution of Linkage for Irregular Phenotype Systems. Human Heredity. 31(1). 3–7. 24 indexed citations

20.

Lalouel, J.-M.. (1980). Probability Calculations in Pedigrees under Complex Modes of Inheritance. Human Heredity. 30(5). 320–323. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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