Maris Laan - Concepedia

Author

Maris Laan

Also Known As

Cristen J. Willer, H. Karro, Jing Hua Zhao, John Attia, Laan M, Laan, Maris, M Laan, M. H. Pinard-van der Laan, M. Laan, M.-H Pinard-van der Laan

220

Publications

13.8K

Citations

H-Index

123

Concepts

All Affiliations

University of Tartu Tartu University Hospital University of Helsinki Institute for Molecular Medicine Finland University of Leicester

About

Maris Laan is an author at University of Tartu specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	26	2.1K
2	Public Health	12	15	1.9K
3	Natural Sciences	3	3	47
4	Education	1	1	12
5	Biochemistry	1	1	18

Maris Laan

Publications

6.3K

Citations

H-Index

Page 1

	Year	Citations
Genome-wide association study identifies eight loci associated with blood pressure Christopher Newton‐Cheh, Toby Johnson, Vesela Gateva, Nature Genetics Genome-wide Association StudyEpidemiologyGenetic DeterminantBlood PressureGenotype-phenotype Association	2009	1.2K
Causes of male infertility: a 9-year prospective monocentre study on 1737 patients with reduced total sperm counts Margus Punab, Olev Poolamets, Petri Paju, Human Reproduction	2016	409
Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near UMOD Associated with Hypertension Sandosh Padmanabhan, Olle Melander, Toby Johnson, PLoS Genetics	2010	403
SLC2A9 Is a High-Capacity Urate Transporter in Humans Mark J. Caulfield, Patricia B. Munroe, Deb O'Neill, PLoS Medicine	2008	375
Demographic history and linkage disequilibrium in human populations Maris Laan, Svante Pääbo Nature Genetics Population HistoryPopulation ScienceEvolutionary BiologyHistorical DemographyDemographic History	1997	197
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Elin Org, S. Eyheramendy, Peeter Juhanson, Human Molecular Genetics	2009	187
Genetics of Recurrent Miscarriage: Challenges, Current Knowledge, Future Directions Kristiina Rull, Liina Nagirnaja, Maris Laan Frontiers in Genetics	2012	154
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits Jacob M. Keaton, Zoha Kamali, Tian Xie, Nature Genetics	2024	150
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia Laura Kasak, Margus Punab, Liina Nagirnaja, The American Journal of Human Genetics Allelic VariantGenetic DisorderMedicineGeneticsPathogenesis	2018	127
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes Siim Sõber, Mario Reiman, Triin Kikas, Scientific Reports	2015	126

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