Philip Awadalla - Publications

2007-2015 Pediatrics Université de Montréal, Montréal, Canada 
 2015- Molecular Genetics University of Toronto, Toronto, ON, Canada 
Population Genetics, Evolution, Disease Genomics

75 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.748
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  0.596
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  0.662
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  0.753
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  0.421
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  0.715
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  0.778
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  0.792
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  0.579
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  0.663
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  0.708
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  0.726
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  0.803
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  0.498
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  0.521
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  0.484
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