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1
Murine gut microbiota is defined by host genetics and modulates variation of metabolic traits
Murine gut microbiota is defined by host genetics and modulates variation of metabolic traits
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Murine gut microbiota is defined by host genetics and modulates variation of metabolic traits

McKnite, Autumn M ; Perez-Munoz, Maria Elisa ; Lu, Lu ; Williams, Evan G ; Brewer, Simon ; Andreux, Pénélope A ; Bastiaansen, John W M ; Wang, Xusheng ; Kachman, Stephen D ; Auwerx, Johan ; Williams, Robert W ; Benson, Andrew K ; Peterson, Daniel A ; Ciobanu, Daniel C White, Bryan A.

PloS one, 2012-06, Vol.7 (6), p.e39191-e39191 [Periódico revisado por pares]

United States: Public Library of Science

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2
Transcriptional profiling at whole population and single cell levels reveals somatosensory neuron molecular diversity
Transcriptional profiling at whole population and single cell levels reveals somatosensory neuron molecular diversity
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Transcriptional profiling at whole population and single cell levels reveals somatosensory neuron molecular diversity

Chiu, Isaac M ; Barrett, Lee B ; Williams, Erika K ; Strochlic, David E ; Lee, Seungkyu ; Weyer, Andy D ; Lou, Shan ; Bryman, Gregory S ; Roberson, David P ; Ghasemlou, Nader ; Piccoli, Cara ; Ahat, Ezgi ; Wang, Victor ; Cobos, Enrique J ; Stucky, Cheryl L ; Ma, Qiufu ; Liberles, Stephen D ; Woolf, Clifford J

eLife, 2014-12, Vol.3 [Periódico revisado por pares]

England: eLife Sciences Publications Ltd

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3
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
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Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Scholl, Ute I ; Stölting, Gabriel ; Nelson-Williams, Carol ; Vichot, Alfred A ; Choi, Murim ; Loring, Erin ; Prasad, Manju L ; Goh, Gerald ; Carling, Tobias ; Juhlin, C Christofer ; Quack, Ivo ; Rump, Lars C ; Thiel, Anne ; Lande, Marc ; Frazier, Britney G ; Rasoulpour, Majid ; Bowlin, David L ; Sethna, Christine B ; Trachtman, Howard ; Fahlke, Christoph ; Lifton, Richard P

eLife, 2015-04, Vol.4, p.e06315-e06315 [Periódico revisado por pares]

England: eLife Sciences Publications Ltd

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4
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Huckins, Laura M ; Dobbyn, Amanda ; Ruderfer, Douglas M ; Hoffman, Gabriel ; Wang, Weiqing ; Pardiñas, Antonio F ; Rajagopal, Veera M ; Als, Thomas D ; T Nguyen, Hoang ; Girdhar, Kiran ; Boocock, James ; Roussos, Panos ; Fromer, Menachem ; Kramer, Robin ; Domenici, Enrico ; Gamazon, Eric R ; Purcell, Shaun ; Demontis, Ditte ; Børglum, Anders D ; Walters, James T R ; O'Donovan, Michael C ; Sullivan, Patrick ; Owen, Michael J ; Devlin, Bernie ; Sieberts, Solveig K ; Cox, Nancy J ; Im, Hae Kyung ; Sklar, Pamela ; Stahl, Eli A

Nature genetics, 2019-04, Vol.51 (4), p.659-674 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Pardiñas, Antonio F ; Holmans, Peter ; Pocklington, Andrew J ; Escott-Price, Valentina ; Ripke, Stephan ; Carrera, Noa ; Legge, Sophie E ; Bishop, Sophie ; Cameron, Darren ; Hamshere, Marian L ; Han, Jun ; Hubbard, Leon ; Lynham, Amy ; Mantripragada, Kiran ; Rees, Elliott ; MacCabe, James H ; McCarroll, Steven A ; Baune, Bernhard T ; Breen, Gerome ; Byrne, Enda M ; Dannlowski, Udo ; Eley, Thalia C ; Hayward, Caroline ; Martin, Nicholas G ; McIntosh, Andrew M ; Plomin, Robert ; Porteous, David J ; Wray, Naomi R ; Caballero, Armando ; Geschwind, Daniel H ; Huckins, Laura M ; Ruderfer, Douglas M ; Santiago, Enrique ; Sklar, Pamela ; Stahl, Eli A ; Won, Hyejung ; Agerbo, Esben ; Als, Thomas D ; Andreassen, Ole A ; Bækvad-Hansen, Marie ; Mortensen, Preben Bo ; Pedersen, Carsten Bøcker ; Børglum, Anders D ; Bybjerg-Grauholm, Jonas ; Djurovic, Srdjan ; Durmishi, Naser ; Pedersen, Marianne Giørtz ; Golimbet, Vera ; Grove, Jakob ; Hougaard, David M ; Mattheisen, Manuel ; Molden, Espen ; Mors, Ole ; Nordentoft, Merete ; Pejovic-Milovancevic, Milica ; Sigurdsson, Engilbert ; Silagadze, Teimuraz ; Hansen, Christine Søholm ; Stefansson, Kari ; Stefansson, Hreinn ; Steinberg, Stacy ; Tosato, Sarah ; Werge, Thomas ; Collier, David A ; Rujescu, Dan ; Kirov, George ; Owen, Michael J ; O'Donovan, Michael C ; Walters, James T R

Nature genetics, 2018-03, Vol.50 (3), p.381-389 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Brain transcriptome variation among behaviorally distinct strains of zebrafish (Danio rerio)
Brain transcriptome variation among behaviorally distinct strains of zebrafish (Danio rerio)
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Brain transcriptome variation among behaviorally distinct strains of zebrafish (Danio rerio)

Drew, Robert E ; Settles, Matthew L ; Churchill, Erin J ; Williams, Shayna M ; Balli, Soniya ; Robison, Barrie D

BMC genomics, 2012-07, Vol.13 (1), p.323-323, Article 323 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles
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Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles

Timberlake, Andrew T ; Choi, Jungmin ; Zaidi, Samir ; Lu, Qiongshi ; Nelson-Williams, Carol ; Brooks, Eric D ; Bilguvar, Kaya ; Tikhonova, Irina ; Mane, Shrikant ; Yang, Jenny F ; Sawh-Martinez, Rajendra ; Persing, Sarah ; Zellner, Elizabeth G ; Loring, Erin ; Chuang, Carolyn ; Galm, Amy ; Hashim, Peter W ; Steinbacher, Derek M ; DiLuna, Michael L ; Duncan, Charles C ; Pelphrey, Kevin A ; Zhao, Hongyu ; Persing, John A ; Lifton, Richard P

eLife, 2016-09, Vol.5 [Periódico revisado por pares]

England: eLife Sciences Publications Ltd

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8
p16 mutation spectrum in the premalignant condition Barrett's esophagus
p16 mutation spectrum in the premalignant condition Barrett's esophagus
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p16 mutation spectrum in the premalignant condition Barrett's esophagus

Paulson, Thomas G ; Galipeau, Patricia C ; Xu, Lianjun ; Kissel, Heather D ; Li, Xiaohong ; Blount, Patricia L ; Sanchez, Carissa A ; Odze, Robert D ; Reid, Brian J Williams, Simon

PloS one, 2008-11, Vol.3 (11), p.e3809-e3809 [Periódico revisado por pares]

United States: Public Library of Science

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9
Genomic diversity of bacteriophages infecting Microbacterium spp
Genomic diversity of bacteriophages infecting Microbacterium spp
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Genomic diversity of bacteriophages infecting Microbacterium spp

Jacobs-Sera, Deborah ; Abad, Lawrence A ; Alvey, Richard M ; Anders, Kirk R ; Aull, Haley G ; Bhalla, Suparna S ; Blumer, Lawrence S ; Bollivar, David W ; Bonilla, J Alfred ; Butela, Kristen A ; Coomans, Roy J ; Cresawn, Steven G ; D'Elia, Tom ; Diaz, Arturo ; Divens, Ashley M ; Edgington, Nicholas P ; Frederick, Gregory D ; Gainey, Maria D ; Garlena, Rebecca A ; Grant, Kenneth W ; Gurney, Susan M R ; Hendrickson, Heather L ; Hughes, Lee E ; Kenna, Margaret A ; Klyczek, Karen K ; Kotturi, Hari ; Mavrich, Travis N ; McKinney, Angela L ; Merkhofer, Evan C ; Moberg Parker, Jordan ; Molloy, Sally D ; Monti, Denise L ; Pape-Zambito, Dana A ; Pollenz, Richard S ; Pope, Welkin H ; Reyna, Nathan S ; Rinehart, Claire A ; Russell, Daniel A ; Shaffer, Christopher D ; Sivanathan, Viknesh ; Stoner, Ty H ; Stukey, Joseph ; Sunnen, C Nicole ; Tolsma, Sara S ; Tsourkas, Philippos K ; Wallen, Jamie R ; Ware, Vassie C ; Warner, Marcie H ; Washington, Jacqueline M ; Westover, Kristi M ; Whitefleet-Smith, JoAnn L ; Wiersma-Koch, Helen I ; Williams, Daniel C ; Zack, Kira M ; Hatfull, Graham F Cloeckaert, Axel

PloS one, 2020-06, Vol.15 (6), p.e0234636-e0234636 [Periódico revisado por pares]

United States: Public Library of Science

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10
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
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Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

Cruchaga, Carlos ; Haller, Gabe ; Chakraverty, Sumitra ; Mayo, Kevin ; Vallania, Francesco L M ; Mitra, Robi D ; Faber, Kelley ; Williamson, Jennifer ; Bird, Tom ; Diaz-Arrastia, Ramon ; Foroud, Tatiana M ; Boeve, Bradley F ; Graff-Radford, Neill R ; St Jean, Pamela ; Lawson, Michael ; Ehm, Margaret G ; Mayeux, Richard ; Goate, Alison M Toft, Mathias

PloS one, 2012-02, Vol.7 (2), p.e31039-e31039 [Periódico revisado por pares]

United States: Public Library of Science

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