Lathrop, Mark

Nicotine consumption is regulated by a human polymorphism in dopamine neurons

Morel, C., Fattore, L., Pons, S., Hay, Y. A., Marti, F., Lambolez, B., De Biasi, M., Lathrop, M., Fratta, W., Maskos, U., et al. (2014) · Molecular Psychiatry

Nicotinic Acetylcholine Receptors StudySmoking Behavior and Cessation

Cited by 123

Blunted ventral striatal responses to anticipated rewards foreshadow problematic drug use in novelty-seeking adolescents

Büchel, C., Peters, J., Banaschewski, T., Bokde, A. L. W., Bromberg, U., Conrod, P. J., Flor, H., Papadopoulos, D., Garavan, H., Gowland, P., et al. (2017) · Nature Communications

Neurotransmitter Receptor Influence on BehaviorNeural and Behavioral Psychology Studies

Cited by 118

Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

Yu Chen, H., Dina, C., Small, A. M., Shaffer, C. M., Levinson, R. T., Helgadóttir, A., Capoulade, R., Munter, H. M., Martinsson, A., Cairns, B. J., et al. (2023) · European Heart Journal

Cardiac Valve Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 116

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

Priebe, L., Degenhardt, F. A., Herms, S., Haenisch, B., Mattheisen, M., Nieratschker, V, Weingarten, M., Witt, S., Breuer, R., Paul, T., et al. (2012) · Molecular Psychiatry

Bipolar Disorder and TreatmentGenomic variations and chromosomal abnormalities

Cited by 84

ABCA7 rare variants and Alzheimer disease risk

Le Guennec, K., Nicolas, G., Quenez, O., Charbonnier, C., Wallon, D., Bellenguez, C., Grenier-Boley, B., Rousseau, S., Richard, A.-C., Rovelet-Lecrux, A., et al. (2016) · Neurology

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 69

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project

Oudot‐Mellakh, T., Cohen, W., Germain, M., Saut, N., Kallel, C., Zelenika, D., Lathrop, M., Trégouët, D., & Morange, P. (2012) · British Journal of Haematology

Blood Coagulation and Thrombosis MechanismsGenetic Associations and Epidemiology

Cited by 68

Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis

Chen, H. Y., Cairns, B. J., Small, A. M., Burr, H. A., Ambikkumar, A., Martinsson, A., Thériault, S., Munter, H. M., Steffen, B., Zhang, R., et al. (2020) · JAMA Cardiology

Cardiac Valve Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 65

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis

Sarnowski, C., Laprise, C., Malerba, G., Moffatt, M. F., Dizier, M.-H., Morin, A., Vincent, Q. B., Rohde, K., Esparza-Gordillo, J., Margaritte-Jeannin, P., et al. (2016) · Journal of Allergy and Clinical Immunology

Asthma and respiratory diseasesGenetic Associations and Epidemiology

Cited by 35

A Genome-Wide Association Study of the Protein C Anticoagulant Pathway

Athanasiadis, G., Buil, A., Souto, J. C., Borrell, M., López, S., Martinez-Perez, A., Lathrop, M., Fontcuberta, J., Almasy, L., & Soria, J. M. (2011) · PLoS ONE

Blood Coagulation and Thrombosis MechanismsGenetic Associations and Epidemiology

Cited by 23

Consequences of VHL Loss on Global DNA Methylome

Robinson, C. M., Lefebvre, F., Poon, B. P., Bousard, A., Fan, X., Lathrop, M., Tost, J., Kim, W. Y., Riazalhosseini, Y., & Ohh, M. (2018) · Scientific Reports

Epigenetics and DNA MethylationCancer, Hypoxia, and Metabolism

Cited by 21

Exhaustive Genotyping of the Interleukin‐1 Family Genes and Associations with AIDS Progression in a French Cohort

Do, H., Vasilescu, A., Carpentier, W., Meyer, L., Diop, G., Hirtzig, T., Coulonges, C., Labib, T., Spadoni, J., Therwath, A., et al. (2006) · The Journal of Infectious Diseases

HIV Research and TreatmentGenetic Associations and Epidemiology

Cited by 16

A distributed whole genome sequencing benchmark study

Corbett, R. D., Eveleigh, R., Whitney, J., Barai, N., Bourgey, M., Chuah, E., Johnson, J., Moore, R. A., Moradin, N., Mungall, K. L., et al. (2020) · Frontiers in Genetics

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

Cited by 10

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Debette, S., Caro, I., Western, D., Namba, S., Sun, N., Kawaguchi, S., He, Y., Fujita, M., Roshchupkin, G., D'Aoust, T., et al. (2024) · Research Square

Cerebrovascular and genetic disordersMultiple Sclerosis Research Studies

Cited by 5