Year |
Citation |
Score |
2023 |
Murphy TJ, Swail H, Jain J, Anderson M, Awadalla P, Behl L, Brown PE, Charlton CL, Colwill K, Drews SJ, Gingras AC, Hinshaw D, Jha P, Kanji JN, Kirsh VA, et al. The evolution of SARS-CoV-2 seroprevalence in Canada: a time-series study, 2020-2023. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 195: E1030-E1037. PMID 37580072 DOI: 10.1503/cmaj.230249 |
0.771 |
|
2023 |
Darvishian M, Moustaqim-Barrette A, Awadalla P, Bhatti P, Broet P, McDonald K, Murphy RA, Skead K, Urquhart R, Vena J, Dummer TJB. Provincial variation in colorectal cancer screening adherence in Canada; evidence from the Canadian Partnership for Tomorrow's Health. Frontiers in Oncology. 13: 1113907. PMID 37397357 DOI: 10.3389/fonc.2023.1113907 |
0.751 |
|
2023 |
Hill W, Lim EL, Weeden CE, Lee C, Augustine M, Chen K, Kuan FC, Marongiu F, Evans EJ, Moore DA, Rodrigues FS, Pich O, Bakker B, Cha H, Myers R, ... ... Awadalla P, et al. Lung adenocarcinoma promotion by air pollutants. Nature. 616: 159-167. PMID 37020004 DOI: 10.1038/s41586-023-05874-3 |
0.724 |
|
2023 |
Wang Y, Namba S, Lopera E, Kerminen S, Tsuo K, Läll K, Kanai M, Zhou W, Wu KH, Favé MJ, Bhatta L, Awadalla P, Brumpton B, Deelen P, Hveem K, et al. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts. Cell Genomics. 3: 100241. PMID 36777179 DOI: 10.1016/j.xgen.2022.100241 |
0.749 |
|
2022 |
Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, ... ... Awadalla P, et al. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192. PMID 36777996 DOI: 10.1016/j.xgen.2022.100192 |
0.786 |
|
2022 |
Chen S, Petricca J, Ye W, Guan J, Zeng Y, Cheng N, Gong L, Shen SY, Hua JT, Crumbaker M, Fraser M, Liu S, Bratman SV, van der Kwast T, Pugh T, ... ... Awadalla P, et al. The cell-free DNA methylome captures distinctions between localized and metastatic prostate tumors. Nature Communications. 13: 6467. PMID 36309516 DOI: 10.1038/s41467-022-34012-2 |
0.684 |
|
2022 |
Kirsh VA, Skead K, McDonald K, Kreiger N, Little J, Menard K, McLaughlin J, Mukherjee S, Palmer LJ, Goel V, Purdue MP, Awadalla P. Cohort Profile: The Ontario Health Study (OHS). International Journal of Epidemiology. PMID 35962976 DOI: 10.1093/ije/dyac156 |
0.75 |
|
2022 |
Harwood MP, Alves I, Edgington H, Agbessi M, Bruat V, Soave D, Lamaze FC, Favé MJ, Awadalla P. Recombination affects allele-specific expression of deleterious variants in human populations. Science Advances. 8: eabl3819. PMID 35559670 DOI: 10.1126/sciadv.abl3819 |
0.807 |
|
2021 |
Võsa U, Claringbould A, Westra HJ, Bonder MJ, Deelen P, Zeng B, Kirsten H, Saha A, Kreuzhuber R, Yazar S, Brugge H, Oelen R, de Vries DH, van der Wijst MGP, Kasela S, ... ... Awadalla P, et al. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nature Genetics. PMID 34475573 DOI: 10.1038/s41588-021-00913-z |
0.813 |
|
2021 |
Tremblay J, Haloui M, Attaoua R, Tahir R, Hishmih C, Harvey F, Marois-Blanchet FC, Long C, Simon P, Santucci L, Hizel C, Chalmers J, Marre M, Harrap S, Cífková R, ... ... Awadalla P, et al. Correction to: Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control. Diabetologia. PMID 34448881 DOI: 10.1007/s00125-021-05544-x |
0.751 |
|
2021 |
Skead K, Ang Houle A, Abelson S, Agbessi M, Bruat V, Lin B, Soave D, Shlush L, Wright S, Dick J, Morris Q, Awadalla P. Interacting evolutionary pressures drive mutation dynamics and health outcomes in aging blood. Nature Communications. 12: 4921. PMID 34389724 DOI: 10.1038/s41467-021-25172-8 |
0.801 |
|
2021 |
Tremblay J, Haloui M, Attaoua R, Tahir R, Hishmih C, Harvey F, Marois-Blanchet FC, Long C, Simon P, Santucci L, Hizel C, Chalmers J, Marre M, Harrap S, Cífková R, ... ... Awadalla P, et al. Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control. Diabetologia. PMID 34226943 DOI: 10.1007/s00125-021-05491-7 |
0.76 |
|
2020 |
Calabrese C, Davidson NR, Demircioğlu D, Fonseca NA, He Y, Kahles A, Lehmann KV, Liu F, Shiraishi Y, Soulette CM, Urban L, Greger L, Li S, Liu D, ... ... Awadalla P, et al. Genomic basis for RNA alterations in cancer. Nature. 578: 129-136. PMID 32025019 DOI: 10.1038/S41586-020-1970-0 |
0.339 |
|
2018 |
Ang Houle A, Gibling H, Lamaze FC, Edgington HA, Soave D, Fave MJ, Agbessi M, Bruat V, Stein LD, Awadalla P. Aberrant expression impacts the pan-cancer genomic landscape. Genome Research. PMID 30341163 DOI: 10.1101/Gr.231696.117 |
0.752 |
|
2018 |
Dummer TJB, Awadalla P, Boileau C, Craig C, Fortier I, Goel V, Hicks JMT, Jacquemont S, Knoppers BM, Le N, McDonald T, McLaughlin J, Mes-Masson AM, Nuyt AM, Palmer LJ, et al. The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 190: E710-E717. PMID 29891475 DOI: 10.1503/Cmaj.170292 |
0.32 |
|
2018 |
Favé MJ, Lamaze FC, Soave D, Hodgkinson A, Gauvin H, Bruat V, Grenier JC, Gbeha E, Skead K, Smargiassi A, Johnson M, Idaghdour Y, Awadalla P. Gene-by-environment interactions in urban populations modulate risk phenotypes. Nature Communications. 9: 827. PMID 29511166 DOI: 10.1038/S41467-018-03202-2 |
0.769 |
|
2017 |
Peischl S, Dupanloup I, Foucal A, Jomphe M, Bruat V, Grenier JC, Gouy A, Gilbert KJ, Gbeha E, Bosshard L, Hip-Ki E, Agbessi M, Hodgkinson A, Vézina H, Awadalla P, et al. Relaxed Selection During a Recent Human Expansion. Genetics. PMID 29187508 DOI: 10.1534/Genetics.117.300551 |
0.807 |
|
2017 |
Alves I, Houle AA, Hussin JG, Awadalla P. The impact of recombination on human mutation load and disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372. PMID 29109227 DOI: 10.1098/Rstb.2016.0465 |
0.793 |
|
2017 |
Knowles DA, Davis JR, Edgington H, Raj A, Favé MJ, Zhu X, Potash JB, Weissman MM, Shi J, Levinson DF, Awadalla P, Mostafavi S, Montgomery SB, Battle A. Allele-specific expression reveals interactions between genetic variation and environment. Nature Methods. PMID 28530654 DOI: 10.1038/Nmeth.4298 |
0.795 |
|
2016 |
Hodgkinson A, Grenier JC, Gbeha E, Awadalla P. A haplotype-based normalization technique for the analysis and detection of allele specific expression. Bmc Bioinformatics. 17: 364. PMID 27618913 DOI: 10.1186/s12859-016-1238-8 |
0.724 |
|
2016 |
Kukurba KR, Parsana P, Balliu B, Smith KS, Zappala Z, Knowles DA, Favé MJ, Davis JR, Li X, Zhu X, Potash JB, Weissman MM, Shi J, Kundaje A, Levinson DF, ... Awadalla P, et al. Impact of the X Chromosome and sex on regulatory variation. Genome Research. PMID 27197214 DOI: 10.1101/Gr.197897.115 |
0.791 |
|
2016 |
Merner ND, Mercado A, Khanna AR, Hodgkinson A, Bruat V, Awadalla P, Gamba G, Rouleau GA, Kahle KT. Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia. Journal of Psychiatric Research. 77: 22-26. PMID 26955005 DOI: 10.1016/J.Jpsychires.2016.02.016 |
0.742 |
|
2016 |
Gomez S, Diawara A, Gbeha E, Awadalla P, Sanni A, Idaghdour Y, Rahimy MC. Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings. Frontiers in Pediatrics. 4: 8. PMID 26942167 DOI: 10.3389/Fped.2016.00008 |
0.599 |
|
2015 |
Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, et al. Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. PMID 26493020 DOI: 10.1016/J.Neurobiolaging.2015.09.013 |
0.727 |
|
2015 |
Wünnemann F, Kokta V, Leclerc S, Thibeault M, McCuaig C, Hatami A, Stheneur C, Grenier JC, Awadalla P, Mitchell GA, Andelfinger G, Preuss C. Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome. The Canadian Journal of Cardiology. PMID 26148450 DOI: 10.1016/J.Cjca.2015.04.004 |
0.316 |
|
2015 |
Hussin JG, Hodgkinson A, Idaghdour Y, Grenier JC, Goulet JP, Gbeha E, Hip-Ki E, Awadalla P. Recombination affects accumulation of damaging and disease-associated mutations in human populations. Nature Genetics. 47: 400-4. PMID 25685891 DOI: 10.1038/Ng.3216 |
0.823 |
|
2014 |
Kahle KT, Merner ND, Friedel P, Silayeva L, Liang B, Khanna A, Shang Y, Lachance-Touchette P, Bourassa C, Levert A, Dion PA, Walcott B, Spiegelman D, Dionne-Laporte A, Hodgkinson A, ... Awadalla P, et al. Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy. Embo Reports. 15: 766-74. PMID 24928908 DOI: 10.15252/Embr.201438840 |
0.743 |
|
2014 |
Hodgkinson A, Idaghdour Y, Gbeha E, Grenier JC, Hip-Ki E, Bruat V, Goulet JP, de Malliard T, Awadalla P. High-resolution genomic analysis of human mitochondrial RNA sequence variation. Science (New York, N.Y.). 344: 413-5. PMID 24763589 DOI: 10.1126/Science.1251110 |
0.805 |
|
2014 |
Quinlan J, Idaghdour Y, Goulet JP, Gbeha E, de Malliard T, Bruat V, Grenier JC, Gomez S, Sanni A, Rahimy MC, Awadalla P. Genomic architecture of sickle cell disease in West African children. Frontiers in Genetics. 5: 26. PMID 24592274 DOI: 10.3389/Fgene.2014.00026 |
0.823 |
|
2013 |
Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, de Maillard T, Grenier JC, Grenier JC, Gbeha E, Hamdan FF, Girard S, Spinella JF, Larivière M, Saillour V, Healy J, ... ... Awadalla P, et al. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. Plos Genetics. 9: e1003815. PMID 24086152 DOI: 10.1371/Journal.Pgen.1003815 |
0.816 |
|
2013 |
Hodgkinson A, Casals F, Idaghdour Y, Grenier JC, Hernandez RD, Awadalla P. Selective constraint, background selection, and mutation accumulation variability within and between human populations. Bmc Genomics. 14: 495. PMID 23875710 DOI: 10.1186/1471-2164-14-495 |
0.817 |
|
2013 |
Zilversmit MM, Chase EK, Chen DS, Awadalla P, Day KP, McVean G. Hypervariable antigen genes in malaria have ancient roots. Bmc Evolutionary Biology. 13: 110. PMID 23725540 DOI: 10.1186/1471-2148-13-110 |
0.783 |
|
2013 |
Samuels ME, Majewski J, Alirezaie N, Fernandez I, Casals F, Patey N, Decaluwe H, Gosselin I, Haddad E, Hodgkinson A, Idaghdour Y, Marchand V, Michaud JL, Rodrigue MA, Desjardins S, ... ... Awadalla P, et al. Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia. Journal of Medical Genetics. 50: 324-9. PMID 23423984 DOI: 10.1136/Jmedgenet-2012-101483 |
0.805 |
|
2013 |
Hussin J, Sinnett D, Casals F, Idaghdour Y, Bruat V, Saillour V, Healy J, Grenier JC, de Malliard T, Busche S, Spinella JF, Larivière M, Gibson G, Andersson A, Holmfeldt L, ... ... Awadalla P, et al. Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Research. 23: 419-30. PMID 23222848 DOI: 10.1101/Gr.144188.112 |
0.806 |
|
2013 |
Awadalla P, Boileau C, Payette Y, Idaghdour Y, Goulet JP, Knoppers B, Hamet P, Laberge C. Cohort profile of the CARTaGENE study: Quebec's population-based biobank for public health and personalized genomics. International Journal of Epidemiology. 42: 1285-99. PMID 23071140 DOI: 10.1093/Ije/Dys160 |
0.665 |
|
2013 |
Yauk CL, Lucas Argueso J, Auerbach SS, Awadalla P, Davis SR, Demarini DM, Douglas GR, Dubrova YE, Elespuru RK, Glover TW, Hales BF, Hurles ME, Klein CB, Lupski JR, Manchester DK, et al. Harnessing genomics to identify environmental determinants of heritable disease. Mutation Research. 752: 6-9. PMID 22935230 DOI: 10.1016/J.Mrrev.2012.08.002 |
0.417 |
|
2013 |
Hitz M, Lemieux-Perreault L, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras J, Thibeault M, Chetaille P, Montpetit A, Khairy P, ... ... Awadalla P, et al. Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease Plos Genetics. 9. DOI: 10.1371/Annotation/8Bc63544-9Ed4-42Ca-A830-E8058Ab13Bab |
0.755 |
|
2013 |
Capredon M, Preuss C, Grenier J, Bruat V, de Malliard T, Leclerc S, Privé C, Thibeault M, Chetaille P, Samuel M, Awadalla P, Andelfinger G. Impact of Rare Genetic Variations on Left Ventricular Outflow Tract Obstruction: Lessons From Whole Exome Sequencing Canadian Journal of Cardiology. 29: S243. DOI: 10.1016/J.Cjca.2013.07.393 |
0.31 |
|
2013 |
Preuss C, Capredon M, Asselin G, Dubé M, Samuels M, Awadalla P, Chetaille P, Andelfinger G. Linkage Mapping and Whole-Exome Sequencing in a Family With Left Ventricular Outflow Tract Obstruction Canadian Journal of Cardiology. 29: S88. DOI: 10.1016/J.Cjca.2013.07.098 |
0.422 |
|
2013 |
Preuss C, Yang S, Capredon M, Samuels M, Awadalla P, Chetaille P, Andelfinger G. Composite Effects of Rare Variants in a Novel X-Linked Form of Congenital Heart Disease in the Québec Founder Population Canadian Journal of Cardiology. 29: S87. DOI: 10.1016/J.Cjca.2013.07.097 |
0.307 |
|
2012 |
Idaghdour Y, Awadalla P. Exploiting gene expression variation to capture gene-environment interactions for disease. Frontiers in Genetics. 3: 228. PMID 23755064 DOI: 10.3389/Fgene.2012.00228 |
0.717 |
|
2012 |
Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, ... ... Awadalla P, et al. Rare copy number variants contribute to congenital left-sided heart disease. Plos Genetics. 8: e1002903. PMID 22969434 DOI: 10.1371/Journal.Pgen.1002903 |
0.78 |
|
2012 |
Idaghdour Y, Quinlan J, Goulet JP, Berghout J, Gbeha E, Bruat V, de Malliard T, Grenier JC, Gomez S, Gros P, Rahimy MC, Sanni A, Awadalla P. Evidence for additive and interaction effects of host genotype and infection in malaria. Proceedings of the National Academy of Sciences of the United States of America. 109: 16786-93. PMID 22949651 DOI: 10.1073/Pnas.1204945109 |
0.794 |
|
2012 |
Cartwright RA, Hussin J, Keebler JE, Stone EA, Awadalla P. A family-based probabilistic method for capturing de novo mutations from high-throughput short-read sequencing data. Statistical Applications in Genetics and Molecular Biology. 11. PMID 22499693 DOI: 10.2202/1544-6115.1713 |
0.813 |
|
2012 |
Casals F, Idaghdour Y, Hussin J, Awadalla P. Next-generation sequencing approaches for genetic mapping of complex diseases. Journal of Neuroimmunology. 248: 10-22. PMID 22285396 DOI: 10.1016/J.Jneuroim.2011.12.017 |
0.791 |
|
2012 |
Ivanga M, Sandoval J, Idaghdour Y, Corbeil G, Awadalla P, Seda O, Chalmers J, Harrap S, McMahon S, Marre M, Gaudet D, Tremblay J, Hamet P. 70 17q21.31 CNV DOSE DEPENDENT EFFECT ON THE PREVALENCE OF HYPERTENSION AND DYSLIPIDEMIA COMORBIDITY Journal of Hypertension. 30: e22. DOI: 10.1097/01.Hjh.0000419895.80861.Ec |
0.583 |
|
2011 |
Hussin J, Roy-Gagnon MH, Gendron R, Andelfinger G, Awadalla P. Age-dependent recombination rates in human pedigrees. Plos Genetics. 7: e1002251. PMID 21912527 DOI: 10.1371/Journal.Pgen.1002251 |
0.664 |
|
2011 |
Casals F, Sikora M, Laayouni H, Montanucci L, Muntasell A, Lazarus R, Calafell F, Awadalla P, Netea MG, Bertranpetit J. Genetic adaptation of the antibacterial human innate immunity network. Bmc Evolutionary Biology. 11: 202. PMID 21745391 DOI: 10.1186/1471-2148-11-202 |
0.657 |
|
2011 |
Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, ... ... Awadalla P, et al. Variation in genome-wide mutation rates within and between human families. Nature Genetics. 43: 712-4. PMID 21666693 DOI: 10.1038/Ng.862 |
0.788 |
|
2011 |
Laayouni H, Montanucci L, Sikora M, Melé M, Dall'Olio GM, Lorente-Galdos B, McGee KM, Graffelman J, Awadalla P, Bosch E, Comas D, Navarro A, Calafell F, Casals F, Bertranpetit J. Similarity in recombination rate estimates highly correlates with genetic differentiation in humans. Plos One. 6: e17913. PMID 21464928 DOI: 10.1371/Journal.Pone.0017913 |
0.701 |
|
2011 |
Jiang H, Li N, Gopalan V, Zilversmit MM, Varma S, Nagarajan V, Li J, Mu J, Hayton K, Henschen B, Yi M, Stephens R, McVean G, Awadalla P, Wellems TE, et al. High recombination rates and hotspots in a Plasmodium falciparum genetic cross. Genome Biology. 12: R33. PMID 21463505 DOI: 10.1186/Gb-2011-12-4-R33 |
0.783 |
|
2011 |
Myers RA, Casals F, Gauthier J, Hamdan FF, Keebler J, Boyko AR, Bustamante CD, Piton AM, Spiegelman D, Henrion E, Zilversmit M, Hussin J, Quinlan J, Yang Y, Lafrenière RG, ... ... Awadalla P, et al. A population genetic approach to mapping neurological disorder genes using deep resequencing. Plos Genetics. 7: e1001318. PMID 21383861 DOI: 10.1371/Journal.Pgen.1001318 |
0.796 |
|
2011 |
Branch OH, Sutton PL, Barnes C, Castro JC, Hussin J, Awadalla P, Hijar G. Plasmodium falciparum genetic diversity maintained and amplified over 5 years of a low transmission endemic in the Peruvian Amazon. Molecular Biology and Evolution. 28: 1973-86. PMID 21109587 DOI: 10.1093/Molbev/Msq311 |
0.71 |
|
2010 |
Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR, Côté M, Henrion E, Spiegelman D, Tarabeux J, Piton A, Yang Y, Boyko A, Bustamante C, Xiong L, et al. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. American Journal of Human Genetics. 87: 316-24. PMID 20797689 DOI: 10.1016/J.Ajhg.2010.07.019 |
0.8 |
|
2010 |
Guernsey DL, Jiang H, Hussin J, Arnold M, Bouyakdan K, Perry S, Babineau-Sturk T, Beis J, Dumas N, Evans SC, Ferguson M, Matsuoka M, Macgillivray C, Nightingale M, Patry L, ... ... Awadalla P, et al. Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. American Journal of Human Genetics. 87: 40-51. PMID 20598275 DOI: 10.1016/J.Ajhg.2010.06.003 |
0.727 |
|
2010 |
Zilversmit MM, Volkman SK, DePristo MA, Wirth DF, Awadalla P, Hartl DL. Low-complexity regions in Plasmodium falciparum: missing links in the evolution of an extreme genome. Molecular Biology and Evolution. 27: 2198-209. PMID 20427419 DOI: 10.1093/Molbev/Msq108 |
0.804 |
|
2010 |
Gauthier J, Champagne N, Lafrenière RG, Xiong L, Spiegelman D, Brustein E, Lapointe M, Peng H, Côté M, Noreau A, Hamdan FF, Addington AM, Rapoport JL, Delisi LE, Krebs MO, ... ... Awadalla P, et al. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 107: 7863-8. PMID 20385823 DOI: 10.1073/Pnas.0906232107 |
0.364 |
|
2010 |
Mu J, Myers RA, Jiang H, Liu S, Ricklefs S, Waisberg M, Chotivanich K, Wilairatana P, Krudsood S, White NJ, Udomsangpetch R, Cui L, Ho M, Ou F, Li H, ... ... Awadalla P, et al. Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs. Nature Genetics. 42: 268-71. PMID 20101240 DOI: 10.1038/Ng.528 |
0.579 |
|
2008 |
Prugnolle F, McGee K, Keebler J, Awadalla P. Selection shapes malaria genomes and drives divergence between pathogens infecting hominids versus rodents. Bmc Evolutionary Biology. 8: 223. PMID 18667061 DOI: 10.1186/1471-2148-8-223 |
0.723 |
|
2007 |
Bockhorst J, Lu F, Janes JH, Keebler J, Gamain B, Awadalla P, Su Xz, Samudrala R, Jojic N, Smith JD. Structural polymorphism and diversifying selection on the pregnancy malaria vaccine candidate VAR2CSA Molecular and Biochemical Parasitology. 155: 103-112. PMID 17669514 DOI: 10.1016/J.Molbiopara.2007.06.007 |
0.739 |
|
2007 |
Mu J, Awadalla P, Duan J, McGee KM, Keebler J, Seydel K, McVean GA, Su XZ. Genome-wide variation and identification of vaccine targets in the Plasmodium falciparum genome. Nature Genetics. 39: 126-30. PMID 17159981 DOI: 10.1038/Ng1924 |
0.756 |
|
2006 |
Jackson M, Watt AJ, Gautier P, Gilchrist D, Driehaus J, Graham GJ, Keebler J, Prugnolle F, Awadalla P, Forrester LM. A murine specific expansion of the Rhox cluster involved in embryonic stem cell biology is under natural selection. Bmc Genomics. 7: 212. PMID 16916441 DOI: 10.1186/1471-2164-7-212 |
0.712 |
|
2006 |
Trimnell AR, Kraemer SM, Mukherjee S, Phippard DJ, Janes JH, Flamoe E, Su XZ, Awadalla P, Smith JD. Global genetic diversity and evolution of var genes associated with placental and severe childhood malaria. Molecular and Biochemical Parasitology. 148: 169-80. PMID 16697476 DOI: 10.1016/J.Molbiopara.2006.03.012 |
0.351 |
|
2006 |
Carbone MA, Jordan KW, Lyman RF, Harbison ST, Leips J, Morgan TJ, DeLuca M, Awadalla P, Mackay TF. Phenotypic variation and natural selection at catsup, a pleiotropic quantitative trait gene in Drosophila. Current Biology : Cb. 16: 912-9. PMID 16682353 DOI: 10.1016/J.Cub.2006.03.051 |
0.436 |
|
2005 |
Mu J, Awadalla P, Duan J, McGee KM, Joy DA, McVean GA, Su XZ. Recombination hotspots and population structure in Plasmodium falciparum. Plos Biology. 3: e335. PMID 16144426 DOI: 10.1371/Journal.Pbio.0030335 |
0.431 |
|
2004 |
Barbash DA, Awadalla P, Tarone AM. Functional divergence caused by ancient positive selection of a Drosophila hybrid incompatibility locus. Plos Biology. 2: e142. PMID 15208709 DOI: 10.1371/Journal.Pbio.0020142 |
0.344 |
|
2004 |
Haydon DT, Bastos AD, Awadalla P. Low linkage disequilibrium indicative of recombination in foot-and-mouth disease virus gene sequence alignments. The Journal of General Virology. 85: 1095-100. PMID 15105526 DOI: 10.1099/Vir.0.19588-0 |
0.358 |
|
2003 |
Charlesworth D, Mable BK, Schierup MH, Bartolomé C, Awadalla P. Diversity and linkage of genes in the self-incompatibility gene family in Arabidopsis lyrata. Genetics. 164: 1519-35. PMID 12930757 |
0.499 |
|
2001 |
Eyre-Walker A, Awadalla P. Does human mtDNA recombine? Journal of Molecular Evolution. 53: 430-435. PMID 11675602 DOI: 10.1007/S002390010232 |
0.587 |
|
2001 |
Schierup MH, Mable BK, Awadalla P, Charlesworth D. Identification and characterization of a polymorphic receptor kinase gene linked to the self-incompatibility locus of Arabidopsis lyrata. Genetics. 158: 387-99. PMID 11333247 |
0.499 |
|
2000 |
Kivisild T, Villems R, Jorde LB, Bamshad M, Kumar S, Hedrick P, Dowling T, Stoneking M, Parsons TJ, Irwin JA, Awadalla P, Eyre-Walker A, Smith JM. Questioning evidence for recombination in human mitochondrial DNA. Science (New York, N.Y.). 288: 1931a. PMID 17835098 DOI: 10.1126/Science.288.5473.1931A |
0.52 |
|
2000 |
Charlesworth D, Awadalla P, Mable BK, Schierup MH. Population-level studies of multiallelic serf-incompatibility loci, with particular reference to Brassicaceae Annals of Botany. 85: 227-239. DOI: 10.1006/Anbo.1999.1015 |
0.522 |
|
1999 |
Awadalla P, Eyre-Walker A, Smith JM. Linkage disequilibrium and recombination in hominid mitochondrial DNA Science. 286: 2524-2525. PMID 10617471 DOI: 10.1126/Science.286.5449.2524 |
0.521 |
|
1999 |
Awadalla P, Charlesworth D. Recombination and selection at Brassica self-incompatibility loci Genetics. 152: 413-425. PMID 10224271 |
0.538 |
|
1998 |
Charlesworth D, Awadalla P. Flowering plant self-incompatibility: The molecular population genetics of Brassica S-loci Heredity. 81: 1-9. PMID 9720299 DOI: 10.1038/Sj.Hdy.6884000 |
0.485 |
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