Mark Lathrop

32.8k citations

48 papers · 7.2k indexed · 3 hit papers · h-index 25

Impact in

Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Hemoglobinopathies and Related Disorders
- Genetics and Neurodevelopmental Disorders
- Genetic and phenotypic traits in livestock
Endocrine and Autonomic Systems top 1%
- Circadian rhythm and melatonin

Papers in

Genetics 34
- Genetic Mapping and Diversity in Plants and Animals 14
- Genetic Associations and Epidemiology 14
- Diabetes and associated disorders 7
- Genetic and phenotypic traits in livestock 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
Hematology 5
- Blood Coagulation and Thrombosis Mechanisms 5

Co-authors: Gàbor Gyapay Philippe Millasseau Cécile Fizames Colette Dib Alain Vignal Jean Morissette Nathalie Drouot Eric Seboun
Journals: European Journal of Human Genetics (4 papers)Hypertension (3 papers)The American Journal of Human Genetics (2 papers)Nature Reviews Genetics (2 papers)Genomics (2 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Mark Lathrop

48 papers receiving 7.0k citations

Hit Papers

align trajectories log scale

Mapping complex disease traits with global gene expression 2009 · 578 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2009 Nature Reviews Genetics
1996 Nature
1994 Nature Genetics

Peers

Countries citing papers authored by Mark Lathrop

Since Specialization

Citations

This map shows the geographic impact of Mark Lathrop'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 Mark Lathrop with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Lathrop more than expected).

Fields of papers citing papers by Mark Lathrop

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark Lathrop. 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 Mark Lathrop. The network helps show where Mark Lathrop may publish in the future.

Co-authors

The 25 scholars most cited alongside Mark Lathrop, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mark Lathrop Line = papers co-authored together Mark Lathrop links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genomic variants associated with age at diagnosis of childhood-onset type 1 diabetes Journal of Human Genetics ·Pierre Bougnères, Cristina CURUłIU, Yoichiro Kamatani, Annick Quettier, Marie‐Pierre Belot, 桑野幸徳, (unknown), Xiaojian Shao, Mark Lathrop, Alain‐Jacques Valleron	2024	1
2	Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing Scientific Reports ·Atsuko Imai, Akihiro Nakaya, Somayyeh Fahiminiya, Martine Tétreault, Jacek Majewski, Yasushi Sakata, Seiji Takashima, Mark Lathrop, Jürg Ott	2015	9
3	Association between circadian genes, bipolar disorders and chronotypes Chronobiology International ·Bruno Étain, Stéphane Jamain, Vanessa Milhiet, Mohamed Lajnef, Carole Boudebesse, Anne Dumaine, Flavie Mathieu, Andreas Gombert, Apolline Monfilliette-Djelad, Sébastien Gard, Jean Pierre Kahn, Chantal Henry, Anne Boland, Diana Zélénika, Doris Lechner, Mark Lathrop, Marion Leboyer, Frank Bellivier	2014	59
4	Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence Biological Psychiatry ·Sylvane Desrivières, L. A. Mityuk, Anbarasu Lourdusamy, Francesca Ducci, Paula L. Hoffman, Norbert Wodarz, Monika Ridinger, Marcella Rietschel, Diana Zélénika, Mark Lathrop, Günter Schumann, Boris Tabakoff	2011	17
5	Family-based designs for genome-wide association studies Nature Reviews Genetics ·Jürg Ott, Yoichiro Kamatani, Mark Lathrop	2011	184
6	Genetic analysis of an F2 intercross between two chicken lines divergently selected for body-weight BMC Genomics ·Per Wahlberg, Örjan Carlborg, Mario Foglio, Xavier Tordoir, Ann‐Christine Syvänen, Mark Lathrop, Marta Gut, P.B. Siegel, Leif Andersson	2009	56
7	Mapping complex disease traits with global gene expression Nature Reviews Genetics ·William Cookson, Liming Liang, Gonçalo R. Abecasis, Miriam F. Moffatt, Mark Lathrop Hit paper breakdown →	2009	578
8	A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels Human Genetics ·Maria Sabater‐Lleal, Alfonso Buil, Juan Carlos Souto, Nicole Gintings, Montserrat Borrell, Mark Lathrop, John Blangero, J. Fontcuberta, José Manuel Soria	2008	9
9	Familial generalized epilepsy in Bulgarian Roma Epileptic Disorders ·Ivailo Tournev, 環河越, Pierre Szepetowski, Velina Guergueltcheva, pei cai, Reana Velizarova, Xin Bing Liu, Mark Lathrop, Sarah Jamali, Marta María García Escudero, Margarita Raycheva, Pierre Genton	2007	3
10	A high-resolution linkage map for the Z chromosome in chicken reveals hot spots for recombination Cytogenetic and Genome Research ·Peter Wahlberg, L. Strömstedt, Xavier Tordoir, Mario Foglio, S. K. Heath, Doris Lechner, Susan Rummel, Michèle Tixier‐Boichard, Mark Lathrop, Marta Gut, Leif Andersson	2007	25
11	Missense Mutation in Sterile α Motif of Novel Protein SamCystin is Associated with Polycystic Kidney Disease in (cy/+) Rat Journal of the American Society of Nephrology ·H. S. Miner, Theauthors arewiththeInstitut, Sigrid Hoffmann, 梁岳静, A. Parasacchi, 崔志坤, Mangazeeva Tatiana Nikolaevna, Venkat Raghavan, Pamela J. Kaisaki, Usman O. Akeju, Patrick Danoy, Richard R. Copley, John Broxholme, Ralph Witzgall, Mark Lathrop, Norbert Gretz, Dominique Gauguier	2005	73
12	D6S26515 marks a DRB115, DQB10602 haplotype associated with attenuated protection from type 1 diabetes mellitus Diabetologia* ·Ana M. Valdes, G. Thomson, Jinko Graham, M. Alfath Kaffahmi, Brad McNeney, Ingrid Kockum, Anajane G. Smith, Mark Lathrop, Ann R. Steenkiste, Janice S. Dorman, Janelle A. Noble, John A. Hansen, Alberto Pugliese, Åke Lernmark, (unknown)	2005	17
13	Integration of the Rat Recombination and EST Maps in the Rat Genomic Sequence and Comparative Mapping Analysis With the Mouse Genome Genome Research ·Steven P. Wilder, Marie‐Thérèse Bihoreau, Karène Argoud, Takeshi Watanabe, Mark Lathrop, Dominique Gauguier	2004	18
14	The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption Nature Medicine ·Rainer Spanagel, Gurudutt Pendyala, Carolina Abarca, Tarek Zghoul, Carles Sanchis‐Segura, Maria Chiara Magnone, Jesús Lascorz, Martin Depner, David Holzberg, Michael Soyka, Stefan Schreiber, Fumihiko Matsuda, Mark Lathrop, Günter Schumann, Urs Albrecht	2004	461
15	Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations European Journal of Human Genetics ·Myrna Medlej‐Hashim, Mirna Mustapha, Éliane Chouery, Dominique Weil, Durdane Ozturk, Nabiha Salem, Valérie Delague, Jacques Loiselet, Mark Lathrop, Christine Petit, André Mégarbané	2002	25
16	A Quantitative-Trait Locus in the Human Factor XII Gene Influences Both Plasma Factor XII Levels and Susceptibility to Thrombotic Disease The American Journal of Human Genetics ·José Manuel Soria, Laura Almasy, Juan Carlos Souto, Delphine Bacq, Alfonso Buil, Nicola E. Beaumont, Zhijing Jian, José Mateo, Montserrat Borrell, W. H. Stone, Mark Lathrop, J. Fontcuberta, John Blangero	2002	72
17	Detailed Comparative Gene Map of Rat Chromosome 1 with Mouse and Human Genomes and Physical Mapping of an Evolutionary Chromosomal Breakpoint Genomics ·Pamela J. Kaisaki, Mathias Rouard, Patrick Danoy, Robert H. Wallis, Stephan C. Collins, V. M. SEGARRA, Elaine R. Levy, Mark Lathrop, Marie‐Thérèse Bihoreau, Dominique Gauguier	2000	14
18	Evidence for the Presence of Insulin-Dependent Diabetes-Associated Alleles on the Distal Part of Mouse Chromosome 6 Genome Research ·Evie Melanitou, Florence Joly, Mark Lathrop, Christian Boîtard, Philip Avner	1998	40
19	Localization of tub and uncoupling proteins ( Ucp ) 2 and 3 to a region of rat Chromosome 1 linked to glucose intolerance and adiposity in the Goto-Kakizaki (GK) Type 2 diabetic rat Mammalian Genome ·Pamela J. Kaisaki, Peng Yeong Woon, Robert H. Wallis, Anthony P. Monaco, Mark Lathrop, Dominique Gauguier	1998	21
20	A comprehensive genetic map of the human genome based on 5,264 microsatellites Nature ·Colette Dib, Sabine Fauré, Cécile Fizames, Delphine Samson, Nathalie Drouot, Alain Vignal, Philippe Millasseau, C.L. Baxley, Omar M. Hussain, Eric Seboun, Mark Lathrop, Gàbor Gyapay, Jean Morissette, Jean Weissenbach Hit paper breakdown →	1996	2444

About Mark Lathrop

Mark Lathrop is a scholar working on Genetics, Genetics, Hematology, Endocrine and Autonomic Systems and Biological Psychiatry, having authored 48 papers that have together received 7.2k indexed citations. Recurring topics across this work include Genetic Mapping and Diversity in Plants and Animals (14 papers), Genetic Associations and Epidemiology (14 papers), Diabetes and associated disorders (7 papers), Pancreatic function and diabetes (6 papers), Blood Coagulation and Thrombosis Mechanisms (5 papers), Genetic and phenotypic traits in livestock (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (2.9k citations), Endocrine and Autonomic Systems (534 citations), Genetics (608 citations), Molecular Biology (3.2k citations) and Hematology (452 citations). Mark Lathrop has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Gàbor Gyapay, Philippe Millasseau, Cécile Fizames, Colette Dib, Alain Vignal, Jean Morissette, Nathalie Drouot, Eric Seboun, Delphine Samson and Jean Weissenbach. Their work appears in journals such as European Journal of Human Genetics, Hypertension, The American Journal of Human Genetics, Nature Reviews Genetics and Genomics.

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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