Skip to Content


Filters: First Letter Of Last Name is B  [Clear All Filters]
A [B] C D E F G H I J K L M N O P Q R S T U V W X Y Z   [Show ALL]
Identification of a QTL for adipocyte volume and of shared genetic effects with aspartate aminotransferase., Bose, Tanushree, Voruganti Saroja V., Tejero Elizabeth M., Proffit Michael J., Cox Laura A., VandeBerg John L., Mahaney Michael C., Rogers Jeffrey, Freeland-Graves Jeanne H., Cole Shelley A., et al. , Biochemical genetics, 2010 Jun, Volume 48, Issue 5-6, p.538-47, (2010) Abstract
NR2F1 mutations cause optic atrophy with intellectual disability., Bosch, Daniëlle G. M., Boonstra Nienke F., Gonzaga-Jauregui Claudia, Xu Mafei, de Ligt Joep, Jhangiani Shalini, Wiszniewski Wojciech, Muzny Donna M., Yntema Helger G., Pfundt Rolph, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.303-9, (2014) Abstract
Novel genetic causes for cerebral visual impairment., Bosch, Daniëlle G. M., Boonstra Nienke F., de Leeuw Nicole, Pfundt Rolph, Nillesen Willy M., de Ligt Joep, Gilissen Christian, Jhangiani Shalini, Lupski James R., Cremers Frans P. M., et al. , European journal of human genetics : EJHG, 2015 Sep 9, (2015) Abstract
Draft genome sequences and description of Lactobacillus rhamnosus strains L31, L34, and L35, Boonma, Prapaporn, Spinler Jennifer K., Qin Xiang, Jittaprasatsin Chutima, Muzny Donna M., Doddapaneni Harsha, Gibbs Richard, Petrosino Joe, Tumwasorn Somying, and Versalovic James , Standards in Genomic Sciences, 02/2014, Volume 9, Issue 3, p.744 - 754, (2014)
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles., Boone, Philip M., Campbell Ian M., Baggett Brett C., Soens Zachry T., Rao Mitchell M., Hixson Patricia M., Patel Ankita, Bi Weimin, Cheung Sau Wai, Lalani Seema R., et al. , Genome research, 2013 Sep, Volume 23, Issue 9, p.1383-94, (2013) Abstract
Incidental copy-number variants identified by routine genome testing in a clinical population., Boone, Philip M., Soens Zachry T., Campbell Ian M., Stankiewicz Pawel, Cheung Sau Wai, Patel Ankita, Beaudet Arthur L., Plon Sharon E., Shaw Chad A., McGuire Amy L., et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2013 Jan, Volume 15, Issue 1, p.45-54, (2013) Abstract
Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium., Bonnen, P. E., Story M. D., Ashorn C. L., Buchholz T. A., Weil M. M., and Nelson D. L. , American journal of human genetics, 2000 Dec, Volume 67, Issue 6, p.1437-51, (2000) Abstract
European admixture on the Micronesian island of Kosrae: lessons from complete genetic information., Bonnen, Penelope E., Lowe Jennifer K., Altshuler David M., Breslow Jan L., Stoffel Markus, Friedman Jeffrey M., and Pe'er Itsik , European journal of human genetics : EJHG, 2010 Mar, Volume 18, Issue 3, p.309-16, (2010) Abstract
Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance., Bonnen, Penelope E., Yarham John W., Besse Arnaud, Wu Ping, Faqeih Eissa A., Al-Asmari Ali Mohammad, Saleh Mohammad A. M., Eyaid Wafaa, Hadeel Alrukban, He Langping, et al. , American journal of human genetics, 2013 Sep 5, Volume 93, Issue 3, p.471-81, (2013) Abstract
Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia., Bonnen, Penelope E., Pe'er Itsik, Plenge Robert M., Salit Jackie, Lowe Jennifer K., Shapero Michael H., Lifton Richard P., Breslow Jan L., Daly Mark J., Reich David E., et al. , Nature genetics, 2006 Feb, Volume 38, Issue 2, p.214-7, (2006) Abstract
Haplotype and linkage disequilibrium architecture for human cancer-associated genes., Bonnen, Penelope E., Wang Peggy J., Kimmel Marek, Chakraborty Ranajit, and Nelson David L. , Genome research, 2002 Dec, Volume 12, Issue 12, p.1846-53, (2002) Abstract
Investigation of the conformation of lactate dehydrogenase and of its catalytic activity., Bolotina, I. A., Markovich D. S., Volkenstein M. V., and Zavodzky P. , Biochimica et biophysica acta, 1967 Mar 15, Volume 132, Issue 2, p.271-81, (1967)
Graded phenotypic response to partial and complete deficiency of a brain-specific transcript variant of the winged helix transcription factor RFX4., Blackshear, Perry J., Graves Joan P., Stumpo Deborah J., Cobos Inma, Rubenstein John L. R., and Zeldin Darryl C. , Development (Cambridge, England), 2003 Oct, Volume 130, Issue 19, p.4539-52, (2003) Abstract
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence., Bidichandani, S. I., Purandare S. M., Taylor E. E., Gumin G., Machkhas H., Harati Y., Gibbs R. A., Ashizawa T., and Patel P. I. , Human molecular genetics, 1999 Dec, Volume 8, Issue 13, p.2425-36, (1999) Abstract
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes., Biankin, Andrew V., Waddell Nicola, Kassahn Karin S., Gingras Marie-Claude, Muthuswamy Lakshmi B., Johns Amber L., Miller David K., Wilson Peter J., Patch Ann-Marie, Wu Jianmin, et al. , Nature, 2012 Nov 15, Volume 491, Issue 7424, p.399-405, (2012) Abstract
The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism., Besse, Arnaud, Wu Ping, Bruni Francesco, Donti Taraka, Graham Brett H., Craigen William J., McFarland Robert, Moretti Paolo, Lalani Seema, Scott Kenneth L., et al. , Cell metabolism, 2015 Mar 3, Volume 21, Issue 3, p.417-27, (2015) Abstract
Quantitative trait loci for peripheral blood cell counts: a study in baboons., Bertin, Angéline, Mahaney Michael C., Cox Laura A., Rogers Jeffrey, VandeBerg John L., Brugnara Carlo, and Platt Orah S. , Mammalian genome : official journal of the International Mammalian Genome Society, 2007 May, Volume 18, Issue 5, p.361-72, (2007) Abstract
Genome-wide linkage disequilibrium and haplotype maps., Belmont, John W., and Gibbs Richard A. , American journal of pharmacogenomics : genomics-related research in drug development and clinical practice, 2004, Volume 4, Issue 4, p.253-62, (2004) Abstract
Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators, Bellott, Daniel W., Hughes Jennifer F., Skaletsky Helen, Brown Laura G., Pyntikova Tatyana, Cho Ting-Jan, Koutseva Natalia, Zaghlul Sara, Graves Tina, Rock Susie, et al. , Nature, 4/2014, Volume 508, Issue 7497, p.494 - 499, (2014)
High-resolution identity by descent mapping uncovers the genetic basis for blood pressure differences between spontaneously hypertensive rat lines., Bell, Rebecca, Herring Stacy M., Gokul Nisha, Monita Monique, Grove Megan L., Boerwinkle Eric, and Doris Peter A. , Circulation. Cardiovascular genetics, 2011 Jun, Volume 4, Issue 3, p.223-31, (2011) Abstract
Glucocorticosteroid suppression of alpha1-fetoprotein synthesis in developing rat liver. Evidence for selective gene repression at the transcriptional level., Bélanger, L., Frain M., Baril P., Gingras M. C., Bartkowiak J., and Sala-Trepat J. M. , Biochemistry, 1981 Nov 10, Volume 20, Issue 23, p.6665-72, (1981)
Oncodevelopmental and hormonal regulation of alpha 1-fetoprotein gene expression., Belanger, L., Baril P., Guertin M., Gingras M. C., Gourdeau H., Anderson A., Hamel D., and Boucher J. M. , Advances in enzyme regulation, 1983, Volume 21, p.73-99, (1983) Abstract
FBN1 contributing to familial congenital diaphragmatic hernia., Beck, Tyler F., Campeau Philippe M., Jhangiani Shalini N., Gambin Tomasz, Li Alexander H., Abo-Zahrah Reem, Jordan Valerie K., Hernandez-Garcia Andres, Wiszniewski Wojciech K., Muzny Donna, et al. , American journal of medical genetics. Part A, 2015 Apr, Volume 167, Issue 4, p.831-6, (2015) Abstract
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI., Bayram, Yavuz, Aydin Hatip, Gambin Tomasz, Akdemir Zeynep Coban, Atik Mehmed M., Karaca Ender, Karaman Ali, Pehlivan Davut, Jhangiani Shalini N., Gibbs Richard A., et al. , American journal of medical genetics. Part A, 2015 Apr 6, (2015) Abstract
Homozygous loss-of-function mutations in SOHLH1 in patients with non-syndromic hypergonadotropic hypogonadism., Bayram, Yavuz, Gulsuner Suleyman, Guran Tulay, Abaci Ayhan, Yesil Gozde, Gulsuner Hilal Unal, Atay Zeynep, Pierce Sarah B., Gambin Tomasz, Lee Ming, et al. , The Journal of clinical endocrinology and metabolism, 2015 Mar 16, p.jc20151150, (2015) Abstract

about seo