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Searching for a paternal phenotype for preeclampsia

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DOI
10.1111/aogs.14388
FINNPEC; Jaatinen, Noora; Jääskeläinen, Tiina; Ekholm, Eeva; Laivuori, Hannele
Acta obstetricia et gynecologica scandinavica2022Publicationer information ikon

Evolution of the G Matrix under Nonlinear Genotype-Phenotype Maps

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DOI
10.1086/717814
Milocco, Lisandro; Salazar-Ciudad, Isaac
American Naturalist2022Publicationer information ikon

Yeast Genome-Scale Metabolic Models for Simulating Genotype-Phenotype Relations

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DOI
10.1007/978-3-030-13035-0_5
Castillo, Sandra; Patil, Kiran Raosaheb; Jouhten, Paula
Progress in molecular and subcellular biology2019Publicationer information ikon

MARV : a tool for genome-wide multi-phenotype analysis of rare variants

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10.1186/s12859-017-1530-2
Kaakinen, Marika; Magi, Reedik; Fischer, Krista; Heikkinen, Jani; Järvelin, Marjo-Riitta; Morris, An...
Bmc bioinformatics2017Publicationer information ikon

Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype

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10.1016/j.ejpn.2021.12.012
Ignatius, Erika; Puosi, Riina; Palomäki, Maarit; Forsbom, Noora; Pohjanpelto, Max; Alitalo, Tiina; A...
European journal of paediatric neurology2022Publicationer information ikon

Full-gene haplotypes refine CYP2D6 metabolizer phenotype inferences

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10.1007/s00414-017-1709-0
Wendt, Frank R.; Sajantila, Antti; Moura-Neto, Rodrigo S.; Woerner, August E.; Budowle, Bruce
International Journal of Legal Medicine2018Publicationer information ikon

Structural vertebral endplate nomenclature and etiology : a study by the ISSLS Spinal Phenotype Focus Group

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DOI
10.1007/s00586-017-5292-3
Zehra, Uruj; Bow, Cora; Lotz, Jeffrey C.; Williams, Frances M. K.; Rajasekaran, S.; Karppinen, Jaro;...
European spine journal2018Publicationer information ikon

Is evolution predictable? Quantitative genetics under complex genotype-phenotype maps

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DOI
10.1111/evo.13907
Milocco, Lisandro; Salazar-Ciudad, Isaac
Evolution2020Publicationer information ikon

Comparing osteonecrosis clinical phenotype, timing, and risk factors in children and young adults treated for acute lymphoblastic leukemia

Referentgranskad
DOI
10.1002/pbc.27300
Mogensen, Signe Sloth; Harila-Saari, Arja; Mäkitie, Outi; Myrberg, Ida Hed; Niinimäki, Riitta; Vestl...
Pediatric blood and cancer2018Publicationer information ikon

Effects of genotype and phenotype in personalized drug therapy

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Pietarinen, Paavo
Dissertationes Scholae Doctoralis Ad Sanitatem Investigandam Universitatis Helsinkiensis2017

Searching for a paternal phenotype for preeclampsia

Referentgranskad
Öppen tillgång
DOI
10.1111/aogs.14388
2022

Evolution of the G Matrix under Nonlinear Genotype-Phenotype Maps

Referentgranskad
Öppen tillgång
DOI
10.1086/717814
2022

Yeast Genome-Scale Metabolic Models for Simulating Genotype-Phenotype Relations

Referentgranskad
DOI
10.1007/978-3-030-13035-0_5
2019

MARV : a tool for genome-wide multi-phenotype analysis of rare variants

Referentgranskad
Öppen tillgång
DOI
10.1186/s12859-017-1530-2
2017

Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype

Referentgranskad
Öppen tillgång
DOI
10.1016/j.ejpn.2021.12.012
2022

Full-gene haplotypes refine CYP2D6 metabolizer phenotype inferences

Referentgranskad
Öppen tillgång
DOI
10.1007/s00414-017-1709-0
2018

Structural vertebral endplate nomenclature and etiology : a study by the ISSLS Spinal Phenotype Focus Group

Referentgranskad
DOI
10.1007/s00586-017-5292-3
2018

Is evolution predictable? Quantitative genetics under complex genotype-phenotype maps

Referentgranskad
DOI
10.1111/evo.13907
2020

Comparing osteonecrosis clinical phenotype, timing, and risk factors in children and young adults treated for acute lymphoblastic leukemia

Referentgranskad
DOI
10.1002/pbc.27300
2018

Effects of genotype and phenotype in personalized drug therapy

Öppen tillgång
2017