Brett Graham - Publications

Affiliations: 
2009 Department of Psychology University of Delaware, Newark, DE, United States 

135 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
2021 Gradwell MA, Boyle KA, Browne TJ, Bell AM, Leonardo J, Peralta Reyes FS, Dickie AC, Smith KM, Callister RJ, Dayas CV, Hughes DI, Graham BA. Diversity of inhibitory and excitatory parvalbumin interneuron circuits in the dorsal horn. Pain. PMID 34326298 DOI: 10.1097/j.pain.0000000000002422  1
2021 Gladstone DJ, Lindsay MP, Douketis J, Smith EE, Dowlatshahi D, Wein T, Bourgoin A, Cox J, Falconer JB, Graham BR, Labrie M, McDonald L, Mandzia J, Ngui D, Pageau P, et al. Canadian Stroke Best Practice Recommendations: Secondary Prevention of Stroke Update 2020. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-69. PMID 34140063 DOI: 10.1017/cjn.2021.127  0.01
2021 Wilcox J, Skye SM, Graham B, Zabell A, Li XS, Li L, Shelkay S, Fu X, Neale S, O'Laughlin C, Peterson K, Hazen SL, Tang WHW. Dietary Choline Supplements, but Not Eggs, Raise Fasting TMAO Levels in Participants with Normal Renal Function: A Randomized Clinical Trial. The American Journal of Medicine. PMID 33872583 DOI: 10.1016/j.amjmed.2021.03.016  0.01
2021 Meng L, Isohanni P, Shao Y, Graham BH, Hickey SE, Brooks S, Suomalainen A, Joset P, Steindl K, Rauch A, Hackenberg A, High FA, Armstrong-Javors A, Mencacci NE, Gonzàlez-Latapi P, et al. MED27 variansts cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia. Annals of Neurology. PMID 33443317 DOI: 10.1002/ana.26019  1
2021 Phelps JS, Hildebrand DGC, Graham BJ, Kuan AT, Thomas LA, Nguyen TM, Buhmann J, Azevedo AW, Sustar A, Agrawal S, Liu M, Shanny BL, Funke J, Tuthill JC, Lee WA. Reconstruction of motor control circuits in adult Drosophila using automated transmission electron microscopy. Cell. PMID 33400916 DOI: 10.1016/j.cell.2020.12.013  0.01
2020 Joo W, Vivian MD, Graham BJ, Soucy ER, Thyme SB. A Customizable Low-Cost System for Massively Parallel Zebrafish Behavioral Phenotyping. Frontiers in Behavioral Neuroscience. 14: 606900. PMID 33536882 DOI: 10.3389/fnbeh.2020.606900  0.01
2020 Browne TJ, Hughes DI, Dayas CV, Callister RJ, Graham BA. Projection Neuron Axon Collaterals in the Dorsal Horn: Placing a New Player in Spinal Cord Pain Processing. Frontiers in Physiology. 11: 560802. PMID 33408637 DOI: 10.3389/fphys.2020.560802  1
2020 Mayhew JA, Cummins MJ, Cresswell ET, Callister RJ, Smith DW, Graham BA. Age-related gene expression changes in lumbar spinal cord: Implications for neuropathic pain. Molecular Pain. 16: 1744806920971914. PMID 33241748 DOI: 10.1177/1744806920971914  1
2020 Graham BA, Hughes DI. Defining populations of dorsal horn interneurons. Pain. 161: 2434-2436. PMID 33065697 DOI: 10.1097/j.pain.0000000000002067  1
2020 Yin W, Brittain D, Borseth J, Scott ME, Williams D, Perkins J, Own CS, Murfitt M, Torres RM, Kapner D, Mahalingam G, Bleckert A, Castelli D, Reid D, Lee WA, ... Graham BJ, et al. A petascale automated imaging pipeline for mapping neuronal circuits with high-throughput transmission electron microscopy. Nature Communications. 11: 4949. PMID 33009388 DOI: 10.1038/s41467-020-18659-3  0.01
2020 Yang K, Forman MR, Graham BH, Monahan PO, Giovannucci EL, De Vivo I, Chan AT, Nan H. Association between pre-diagnostic leukocyte mitochondrial DNA copy number and survival among colorectal cancer patients. Cancer Epidemiology. 68: 101778. PMID 32674053 DOI: 10.1016/j.canep.2020.101778  0.01
2020 Yang K, Forman MR, Monahan PO, Graham BH, Chan AT, Zhang X, De Vivo I, Giovannucci EL, Tabung FK, Nan H. Insulinemic Potential of Lifestyle Is Inversely Associated with Leukocyte Mitochondrial DNA Copy Number in US White Adults. The Journal of Nutrition. PMID 32492151 DOI: 10.1093/Jn/Nxaa146  0.01
2020 Emmerzaal TL, Preston G, Geenen B, Verweij V, Wiesmann M, Vasileiou E, Grüter F, de Groot C, Schoorl J, de Veer R, Roelofs M, Arts M, Hendriksen Y, Klimars E, Donti TR, ... Graham BH, et al. Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male mice. Translational Psychiatry. 10: 176. PMID 32488052 DOI: 10.1038/s41398-020-0858-y  1
2020 Madden JF, Davis OC, Boyle KA, Iredale JA, Browne TJ, Callister RJ, Smith DW, Jobling P, Hughes DI, Graham BA. Functional and Molecular Analysis of Proprioceptive Sensory Neuron Excitability in Mice. Frontiers in Molecular Neuroscience. 13: 36. PMID 32477061 DOI: 10.3389/Fnmol.2020.00036  1
2020 Stinson JL, Brault JA, Delk PR, Graham BH, Karmazyn B, Hall B, Weaver DD. An apparent new syndrome of extreme short stature, microcephaly, dysmorphic faces, intellectual disability, and a bone dysplasia of unknown etiology. American Journal of Medical Genetics. Part A. PMID 32426895 DOI: 10.1002/ajmg.a.61619  0.01
2020 Browne TJ, Gradwell MA, Iredale JA, Maden JF, Callister RJ, Hughes DI, Dayas CV, Graham BA. Transgenic Cross-Referencing of Inhibitory and Excitatory Interneuron Populations to Dissect Neuronal Heterogeneity in the Dorsal Horn. Frontiers in Molecular Neuroscience. 13: 32. PMID 32362812 DOI: 10.3389/Fnmol.2020.00032  1
2019 Browne TJ, Smith KM, Gradwell MA, Iredale JA, Dayas CV, Callister RJ, Hughes DI, Graham BA. Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn. Pain. PMID 33779126 DOI: 10.1097/j.pain.0000000000002194  1
2019 Smith KM, Browne TJ, Davis OC, Coyle A, Boyle KA, Watanabe M, Dickinson SA, Iredale JA, Gradwell MA, Jobling P, Callister RJ, Dayas CV, Hughes DI, Graham BA. Calretinin positive neurons form an excitatory amplifier network in the spinal cord dorsal horn. Elife. 8. PMID 31713514 DOI: 10.7554/Elife.49190  1
2019 Callister RJ, Brichta AM, Schaefer AT, Graham BA, Stuart DG. Pioneers in CNS inhibition: 2. Charles Sherrington and John Eccles on inhibition in spinal and supraspinal structures. Brain Research. 146540. PMID 31704081 DOI: 10.1016/J.Brainres.2019.146540  1
2019 Griffin C, Ammous Z, Vance GH, Graham BH, Miller MJ. Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 1128: 121786. PMID 31518899 DOI: 10.1016/j.jchromb.2019.121786  1
2019 Castelluccio VJ, Vetrini F, Lynnes T, Jones J, Holloway L, Belonis A, Breman AM, Graham BH, Sapp K, Wilson T, Schwartz CE, Pratt VM, Weaver DD. An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3. American Journal of Medical Genetics. Part A. PMID 31512387 DOI: 10.1002/ajmg.a.61353  0.01
2019 Flex E, Martinelli S, Van Dijck A, Ciolfi A, Cecchetti S, Coluzzi E, Pannone L, Andreoli C, Radio FC, Pizzi S, Carpentieri G, Bruselles A, Catanzaro G, Pedace L, Miele E, ... ... Graham BH, et al. Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging. American Journal of Human Genetics. PMID 31447100 DOI: 10.1016/J.Ajhg.2019.07.007  1
2019 Boyle KA, Gradwell MA, Yasaka T, Dickie AC, Polgár E, Ganley RP, Orr DPH, Watanabe M, Abraira VE, Kuehn ED, Zimmerman AL, Ginty DD, Callister RJ, Graham BA, Hughes DI. Defining a Spinal Microcircuit that Gates Myelinated Afferent Input: Implications for Tactile Allodynia. Cell Reports. 28: 526-540.e6. PMID 31291586 DOI: 10.1016/J.Celrep.2019.06.040  1
2019 Pillai NR, AlDhaheri NS, Ghosh R, Lim J, Streff H, Nayak A, Graham BH, Hanchard NA, Elsea SH, Scaglia F. Biallelic variants in COX4I1 associated with a novel phenotype resembling Leigh syndrome with developmental regression, intellectual disability, and seizures. American Journal of Medical Genetics. Part A. PMID 31290619 DOI: 10.1002/Ajmg.A.61288  1
2019 Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, et al. Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Medicine. 11: 16. PMID 30909959 DOI: 10.1186/S13073-019-0630-1  1
2019 Mayhew JA, Walker FR, Smith DW, Callister RJ, Graham B. [Express] Ageing alters signalling properties in the mouse spinal dorsal horn. Molecular Pain. 1744806919839860. PMID 30845881 DOI: 10.1177/1744806919839860  1
2019 Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, et al. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Medicine. 11: 12. PMID 30819258 DOI: 10.1186/S13073-019-0623-0  1
2019 Ramachandran PV, Savini M, Folick AK, Hu K, Masand R, Graham BH, Wang MC. Lysosomal Signaling Promotes Longevity by Adjusting Mitochondrial Activity. Developmental Cell. PMID 30713071 DOI: 10.1016/j.devcel.2018.12.022  0.01
2019 Burrage LC, Thistlethwaite L, Stroup BM, Sun Q, Miller MJ, Nagamani SCS, Craigen W, Scaglia F, Sutton VR, Graham B, Kennedy AD, Milosavljevic A, Lee BH, Elsea SH. Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30670878 DOI: 10.1038/S41436-019-0442-0  1
2018 Ng BG, Rosenfeld JA, Emrick L, Jain M, Burrage LC, Lee B, Craigen WJ, Bearden DR, Graham BH, Freeze HH. Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation. American Journal of Human Genetics. PMID 30503518 DOI: 10.1016/J.Ajhg.2018.10.021  1
2018 Wang X, Posey JE, Rosenfeld JA, Bacino CA, Scaglia F, Immken L, Harris JM, Hickey SE, Mosher TM, Slavotinek A, Zhang J, Beuten J, Leduc MS, He W, Vetrini F, ... ... Graham BH, et al. Phenotypic expansion in - a common cause of intellectual disability in females. Annals of Clinical and Translational Neurology. 5: 1277-1285. PMID 30349862 DOI: 10.1002/Acn3.622  1
2018 Yeoh JW, James MH, Adams CD, Bains JS, Sakurai T, Aston-Jones G, Graham BA, Dayas CV. Activation of lateral hypothalamic group III mGluRs suppresses cocaine-seeking following abstinence and normalizes drug-associated increases in excitatory drive to orexin/hypocretin cells. Neuropharmacology. PMID 30253175 DOI: 10.1016/J.Neuropharm.2018.09.033  1
2018 Mullikin D, Pillai N, Sanchez R, O'Donnell-Luria AH, Kritzer A, Tal L, Almannai M, Berry GT, Gambello MJ, Li H, Graham B, Srivaths L, Sutton VR, Grimes A. Megaloblastic Anemia Progressing to Severe Thrombotic Microangiopathy in Patients with Disordered Vitamin B Metabolism: Case Reports and Literature Review. The Journal of Pediatrics. PMID 30057141 DOI: 10.1016/j.jpeds.2018.06.054  1
2018 Graham BR, Menon BK, Coutts SB, Goyal M, Demchuk AM. Computed tomographic angiography in stroke and high-risk transient ischemic attack: Do not leave the emergency department without it! International Journal of Stroke : Official Journal of the International Stroke Society. 1747493018764172. PMID 29664350 DOI: 10.1177/1747493018764172  0.01
2018 Tadros MA, Graham BA, Callister RJ. Moving functional classification of dorsal horn neurons from art to science. The Journal of Physiology. PMID 29524242 DOI: 10.1113/Jp275870  1
2018 Jaiswal M, Haelterman NA, Sandoval H, Xiong B, Donti T, Kalsotra A, Yamamoto S, Cooper TA, Graham BH, Bellen HJ. Correction: Impaired Mitochondrial Energy Production Causes Light-Induced Photoreceptor Degeneration Independent of Oxidative Stress. Plos Biology. 16: e1002622. PMID 29509758 DOI: 10.1371/Journal.Pbio.1002622  1
2018 Larson AA, Balasubramaniam S, Christodoulou J, Burrage LC, Marom R, Graham BH, Diaz GA, Glamuzina E, Hauser N, Heese B, Horvath G, Mattman A, van Karnebeek C, Lane Rutledge S, Williamson A, et al. Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6. Mitochondrion. PMID 29307858 DOI: 10.1016/J.Mito.2018.01.001  1
2017 Landrock KK, Sullivan P, Martini-Stoica H, Goldstein DS, Graham BH, Yamamoto S, Bellen HJ, Gibbs RA, Chen R, D'Amelio M, Stoica G. Pleiotropic Neuropathological and Biochemical Alterations Associated with Myo5a Mutation in a Rat Model. Brain Research. PMID 29217155 DOI: 10.1016/J.Brainres.2017.11.029  1
2017 Peng H, Wang Q, Lou T, Qin J, Jung S, Shetty V, Li F, Wang Y, Feng XH, Mitch WE, Graham BH, Hu Z. Myokine mediated muscle-kidney crosstalk suppresses metabolic reprogramming and fibrosis in damaged kidneys. Nature Communications. 8: 1493. PMID 29138395 DOI: 10.1038/s41467-017-01646-6  0.01
2017 Meng L, Pammi M, Saronwala A, Magoulas P, Ghazi AR, Vetrini F, Zhang J, He W, Dharmadhikari AV, Qu C, Ward P, Braxton A, Narayanan S, Ge X, Tokita MJ, ... ... Graham BH, et al. Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. Jama Pediatrics. e173438. PMID 28973083 DOI: 10.1001/Jamapediatrics.2017.3438  1
2017 Tae HS, Smith KM, Phillips AM, Boyle KA, Li M, Forster IC, Hatch RJ, Richardson R, Hughes DI, Graham BA, Petrou S, Reid CA. Gabapentin Modulates HCN4 Channel Voltage-Dependence. Frontiers in Pharmacology. 8: 554. PMID 28871229 DOI: 10.3389/Fphar.2017.00554  1
2017 Campbell EJ, Mitchell CS, Adams CD, Yeoh JW, Hodgson DM, Graham BA, Dayas CV. Chemogenetic activation of the lateral hypothalamus reverses early life stress-induced deficits in motivational drive. The European Journal of Neuroscience. PMID 28858406 DOI: 10.1111/Ejn.13674  1
2017 Farrell KE, Keely S, Walker MM, Brichta AM, Graham BA, Callister RJ. Altered intrinsic and synaptic properties of lumbosacral dorsal horn neurons in a mouse model of colitis. Neuroscience. PMID 28844004 DOI: 10.1016/J.Neuroscience.2017.08.029  1
2017 Zepeda-Mendoza CJ, Ibn-Salem J, Kammin T, Harris DJ, Rita D, Gripp KW, MacKenzie JJ, Gropman A, Graham B, Shaheen R, Alkuraya FS, Brasington CK, Spence EJ, Masser-Frye D, Bird LM, et al. Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements. American Journal of Human Genetics. PMID 28735859 DOI: 10.1016/J.Ajhg.2017.06.011  0.01
2017 Lai YC, Baker JS, Donti T, Graham BH, Craigen WJ, Anderson AE. Mitochondrial Dysfunction Mediated by Poly(ADP-Ribose) Polymerase-1 Activation Contributes to Hippocampal Neuronal Damage Following Status Epilepticus. International Journal of Molecular Sciences. 18. PMID 28704930 DOI: 10.3390/Ijms18071502  1
2017 Almannai M, Marom R, Divin K, Scaglia F, Sutton VR, Craigen WJ, Lee B, Burrage LC, Graham BH. Milder clinical and biochemical phenotypes associated with the c.482G>A (p.Arg161Gln) pathogenic variant in cobalamin C disease: Implications for management and screening. Molecular Genetics and Metabolism. PMID 28693988 DOI: 10.1016/J.Ymgme.2017.06.011  1
2017 Bainbridge MN, Cooney E, Miller M, Kennedy AD, Wulff JE, Donti T, Jhangiani SN, Gibbs RA, Elsea SH, Porter BE, Graham BH. Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycle. Molecular Genetics and Metabolism. PMID 28673551 DOI: 10.1016/J.Ymgme.2017.06.009  1
2017 Marom R, Jain M, Burrage LC, Song IW, Graham BH, Brown CW, Stevens SJC, Stegmann APA, Gunter AT, Kaplan JD, Gavrilova RH, Shinawi M, Rosenfeld JA, Bae Y, Tran AA, et al. Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Human Mutation. PMID 28649782 DOI: 10.1002/Humu.23282  1
2017 Wangler MF, Chao YH, Bayat V, Giagtzoglou N, Shinde AB, Putluri N, Coarfa C, Donti T, Graham BH, Faust JE, McNew JA, Moser A, Sardiello M, Baes M, Bellen HJ. Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. Plos Genetics. 13: e1006825. PMID 28640802 DOI: 10.1371/Journal.Pgen.1006825  1
2017 Graham BR, Menon BK. Clopidogrel Load Reduces Emboli in Carotid Artery Stenosis With Free-Floating Thrombus. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-3. PMID 28535824 DOI: 10.1017/cjn.2017.48  0.01
2017 Hildebrand DGC, Cicconet M, Torres RM, Choi W, Quan TM, Moon J, Wetzel AW, Scott Champion A, Graham BJ, Randlett O, Plummer GS, Portugues R, Bianco IH, Saalfeld S, Baden AD, et al. Whole-brain serial-section electron microscopy in larval zebrafish. Nature. PMID 28489821 DOI: 10.1038/Nature22356  0.01
2017 Eldomery MK, Coban-Akdemir Z, Harel T, Rosenfeld JA, Gambin T, Stray-Pedersen A, Küry S, Mercier S, Lessel D, Denecke J, Wiszniewski W, Penney S, Liu P, Bi W, Lalani SR, ... ... Graham BH, et al. Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Medicine. 9: 26. PMID 28327206 DOI: 10.1186/S13073-017-0412-6  1
2017 Flynn JR, Conn VL, Boyle KA, Hughes DI, Watanabe M, Velasquez T, Goulding MD, Callister RJ, Graham BA. Anatomical and Molecular Properties of Long Descending Propriospinal Neurons in Mice. Frontiers in Neuroanatomy. 11: 5. PMID 28220062 DOI: 10.3389/Fnana.2017.00005  1
2016 Yoon WH, Sandoval H, Nagarkar-Jaiswal S, Jaiswal M, Yamamoto S, Haelterman NA, Putluri N, Putluri V, Sreekumar A, Tos T, Aksoy A, Donti T, Graham BH, Ohno M, Nishi E, et al. Loss of Nardilysin, a Mitochondrial Co-chaperone for α-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration. Neuron. PMID 28017472 DOI: 10.1016/J.Neuron.2016.11.038  1
2016 Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, ... ... Graham BH, et al. The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature Genetics. PMID 27841880 DOI: 10.1038/Ng.3720  0.01
2016 Potter SL, Venkatramani R, Wenderfer S, Graham BH, Vasudevan SA, Sher A, Wu H, Wheeler DA, Yang Y, Eng CM, Gibbs RA, Roy A, Plon SE, Parsons DW. Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemia. Pediatric Blood & Cancer. PMID 27748010 DOI: 10.1002/Pbc.26286  1
2016 Harel T, Yoon WH, Garone C, Gu S, Coban-Akdemir Z, Eldomery MK, Posey JE, Jhangiani SN, Rosenfeld JA, Cho MT, Fox S, Withers M, Brooks SM, Chiang T, Duraine L, ... ... Graham BH, et al. Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes. American Journal of Human Genetics. PMID 27640307 DOI: 10.1016/J.Ajhg.2016.08.007  1
2016 Donti TR, Masand R, Scott DA, Craigen WJ, Graham BH. Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variant. Molecular Genetics and Metabolism. PMID 27484306 DOI: 10.1016/j.ymgme.2016.07.007  1
2016 Chen K, Lin G, Haelterman NA, Ho TS, Li T, Li Z, Duraine L, Graham BH, Jaiswal M, Yamamoto S, Rasband MN, Bellen HJ. Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration. Elife. 5. PMID 27343351 DOI: 10.7554/Elife.16043  1
2016 Fountain MD, Aten E, Cho MT, Juusola J, Walkiewicz MA, Ray JW, Xia F, Yang Y, Graham BH, Bacino CA, Potocki L, van Haeringen A, Ruivenkamp CA, Mancias P, Northrup H, et al. The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27195816 DOI: 10.1038/Gim.2016.53  1
2016 Graham BR, Shiff N, Nour M, Hasal S, Huntsman R, Almubarak S. Hashimoto Encephalopathy Presenting With Stroke-Like Episodes in an Adolescent Female: A Case Report and Literature Review. Pediatric Neurology. 59: 62-70. PMID 27033176 DOI: 10.1016/j.pediatrneurol.2016.02.003  1
2016 Lee WA, Bonin V, Reed M, Graham BJ, Hood G, Glattfelder K, Reid RC. Anatomy and function of an excitatory network in the visual cortex. Nature. PMID 27018655 DOI: 10.1038/Nature17192  1
2016 Sadat R, Barca E, Masand R, Donti TR, Naini A, De Vivo DC, DiMauro S, Hanchard NA, Graham BH. Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiency. Molecular Genetics and Metabolism. PMID 26992325 DOI: 10.1016/j.ymgme.2016.03.004  1
2016 Whelan KR, Hamilton J, Peeling L, Graham B, Hunter G, Kelly ME. Importance of Developing Stroke Systems of Care to Improve Access to Endovascular Therapies. World Neurosurgery. 88: 678-80. PMID 26944889 DOI: 10.1016/j.wneu.2016.02.098  1
2016 Park JH, Vithayathil S, Kumar S, Sung PL, Dobrolecki LE, Putluri V, Bhat VB, Bhowmik SK, Gupta V, Arora K, Wu D, Tsouko E, Zhang Y, Maity S, Donti TR, ... Graham BH, et al. Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer. Cell Reports. PMID 26923594 DOI: 10.1016/J.Celrep.2016.02.004  1
2016 Montaño AM, Lock-Hock N, Steiner RD, Graham BH, Szlago M, Greenstein R, Pineda M, Gonzalez-Meneses A, Çoker M, Bartholomew D, Sands MS, Wang R, Giugliani R, Macaya A, Pastores G, et al. Clinical course of sly syndrome (mucopolysaccharidosis type VII). Journal of Medical Genetics. PMID 26908836 DOI: 10.1136/Jmedgenet-2015-103322  1
2016 Lalani SR, Liu P, Rosenfeld JA, Watkin LB, Chiang T, Leduc MS, Zhu W, Ding Y, Pan S, Vetrini F, Miyake CY, Shinawi M, Gambin T, Eldomery MK, Akdemir ZH, ... Graham B, et al. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia due to Bi-allelic TANGO2 Mutations. American Journal of Human Genetics. PMID 26805781 DOI: 10.1016/J.Ajhg.2015.12.008  1
2015 Burrage LC, Miller MJ, Wong LJ, Kennedy AD, Sutton VR, Sun Q, Elsea SH, Graham BH. Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma. The Journal of Pediatrics. PMID 26602010 DOI: 10.1016/J.Jpeds.2015.10.045  1
2015 Duchatel RJ, Jobling P, Graham BA, Harms LR, Michie PT, Hodgson DM, Tooney PA. Increased white matter neuron density in a rat model of maternal immune activation - Implications for schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 65: 118-126. PMID 26385575 DOI: 10.1016/J.Pnpbp.2015.09.006  1
2015 Miller MJ, Burrage LC, Gibson JB, Strenk ME, Lose EJ, Bick DP, Elsea SH, Sutton VR, Sun Q, Graham BH, Craigen WJ, Zhang VW, Wong LC. Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States. Molecular Genetics and Metabolism. PMID 26385305 DOI: 10.1016/J.Ymgme.2015.08.011  1
2015 Wu SP, Kao CY, Wang L, Creighton CJ, Yang J, Donti TR, Harmancey R, Vasquez HG, Graham BH, Bellen HJ, Taegtmeyer H, Chang CP, Tsai MJ, Tsai SY. Increased COUP-TFII expression in adult hearts induces mitochondrial dysfunction resulting in heart failure. Nature Communications. 6: 8245. PMID 26356605 DOI: 10.1038/Ncomms9245  1
2015 Ng BG, Raymond K, Kircher M, Buckingham KJ, Wood T, Shendure J, Nickerson DA, Bamshad MJ, Wong JT, Monteiro FP, Graham BH, Jackson S, Sparkes R, Scheuerle AE, Cathey S, et al. Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Human Mutation. PMID 26264460 DOI: 10.1002/Humu.22856  1
2015 Harel T, Posey JE, Graham BH, Walkiewicz M, Yang Y, Lalani SR, Belmont JW. Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant. American Journal of Medical Genetics. Part A. PMID 26198278 DOI: 10.1002/ajmg.a.37230  1
2015 Jaiswal M, Haelterman NA, Sandoval H, Xiong B, Donti T, Kalsotra A, Yamamoto S, Cooper TA, Graham BH, Bellen HJ. Impaired Mitochondrial Energy Production Causes Light-Induced Photoreceptor Degeneration Independent of Oxidative Stress. Plos Biology. 13: e1002197. PMID 26176594 DOI: 10.1371/Journal.Pbio.1002197  1
2015 Tadros MA, Farrell KE, Graham BA, Brichta AM, Callister RJ. Properties of sodium currents in neonatal and young adult mouse superficial dorsal horn neurons. Molecular Pain. 11: 17. PMID 25889748 DOI: 10.1186/S12990-015-0014-5  1
2015 Huemer M, Karall D, Schossig A, Abdenur JE, Al Jasmi F, Biagosch C, Distelmaier F, Freisinger P, Graham BH, Haack TB, Hauser N, Hertecant J, Ebrahimi-Fakhari D, Konstantopoulou V, Leydiker K, et al. Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations. Journal of Inherited Metabolic Disease. PMID 25868664 DOI: 10.1007/S10545-015-9836-6  1
2015 Besse A, Wu P, Bruni F, Donti T, Graham BH, Craigen WJ, McFarland R, Moretti P, Lalani S, Scott KL, Taylor RW, Bonnen PE. The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism. Cell Metabolism. 21: 417-27. PMID 25738457 DOI: 10.1016/J.Cmet.2015.02.008  1
2015 Liu L, Zhang K, Sandoval H, Yamamoto S, Jaiswal M, Sanz E, Li Z, Hui J, Graham BH, Quintana A, Bellen HJ. Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration. Cell. 160: 177-90. PMID 25594180 DOI: 10.1016/J.Cell.2014.12.019  1
2015 Callister RJ, Graham BA. Spicing up the gabapentionoids: facilitating gabapentin entry in spinal pain circuits. Neuroscience Letters. 584: 395-6. PMID 25193581 DOI: 10.1016/J.Neulet.2014.08.039  1
2015 Szafranski P, Von Allmen GK, Graham BH, Wilfong AA, Kang SH, Ferreira JA, Upton SJ, Moeschler JB, Bi W, Rosenfeld JA, Shaffer LG, Wai Cheung S, Stankiewicz P, Lalani SR. 6q22.1 microdeletion and susceptibility to pediatric epilepsy. European Journal of Human Genetics : Ejhg. 23: 173-9. PMID 24824130 DOI: 10.1038/ejhg.2014.75  1
2014 Sandoval H, Yao CK, Chen K, Jaiswal M, Donti T, Lin YQ, Bayat V, Xiong B, Zhang K, David G, Charng WL, Yamamoto S, Duraine L, Graham BH, Bellen HJ. Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production. Elife. 3. PMID 25313867 DOI: 10.7554/Elife.03558  1
2014 Yeoh JW, James MH, Graham BA, Dayas CV. Electrophysiological characteristics of paraventricular thalamic (PVT) neurons in response to cocaine and cocaine- and amphetamine-regulated transcript (CART). Frontiers in Behavioral Neuroscience. 8: 280. PMID 25309361 DOI: 10.3389/Fnbeh.2014.00280  1
2014 Burrage LC, Tang S, Wang J, Donti TR, Walkiewicz M, Luchak JM, Chen LC, Schmitt ES, Niu Z, Erana R, Hunter JV, Graham BH, Wong LJ, Scaglia F. Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 gene. Molecular Genetics and Metabolism. 113: 207-12. PMID 25037980 DOI: 10.1016/J.Ymgme.2014.06.004  1
2014 Harris BM, Hughes DI, Bolton PS, Tadros MA, Callister RJ, Graham BA. Contrasting alterations to synaptic and intrinsic properties in upper-cervical superficial dorsal horn neurons following acute neck muscle inflammation. Molecular Pain. 10: 25. PMID 24725960 DOI: 10.1186/1744-8069-10-25  1
2014 Enns GM, Shashi V, Bainbridge M, Gambello MJ, Zahir FR, Bast T, Crimian R, Schoch K, Platt J, Cox R, Bernstein JA, Scavina M, Walter RS, Bibb A, Jones M, ... Graham BH, et al. Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 751-8. PMID 24651605 DOI: 10.1038/Gim.2014.22  1
2014 Smith KM, Madden JF, Callister RJ, Hughes DI, Graham BA. The search for novel analgesics: re-examining spinal cord circuits with new tools. Frontiers in Pharmacology. 5: 22. PMID 24616699 DOI: 10.3389/Fphar.2014.00022  1
2014 Yeoh JW, Campbell EJ, James MH, Graham BA, Dayas CV. Orexin antagonists for neuropsychiatric disease: progress and potential pitfalls. Frontiers in Neuroscience. 8: 36. PMID 24616658 DOI: 10.3389/Fnins.2014.00036  1
2014 Graham BR, Pylypchuk GB. Posterior reversible encephalopathy syndrome in an adult patient undergoing peritoneal dialysis: a case report and literature review. Bmc Nephrology. 15: 10. PMID 24411012 DOI: 10.1186/1471-2369-15-10  1
2014 Stuart DG, Schaefer AT, Massion J, Graham BA, Callister RJ. Pioneers in CNS inhibition: 1. Ivan M. Sechenov, the first to clearly demonstrate inhibition arising in the brain. Brain Research. 1548: 20-48. PMID 24342718 DOI: 10.1016/J.Brainres.2013.12.006  1
2014 Farrell KE, Keely S, Graham BA, Callister R, Callister RJ. A systematic review of the evidence for central nervous system plasticity in animal models of inflammatory-mediated gastrointestinal pain. Inflammatory Bowel Diseases. 20: 176-95. PMID 24284415 DOI: 10.1097/01.Mib.0000437499.52922.B1  1
2014 Donti TR, Stromberger C, Ge M, Eldin KW, Craigen WJ, Graham BH. Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletion. Disease Models & Mechanisms. 7: 271-80. PMID 24271779 DOI: 10.1242/dmm.013466  1
2013 Bonnen PE, Yarham JW, Besse A, Wu P, Faqeih EA, Al-Asmari AM, Saleh MA, Eyaid W, Hadeel A, He L, Smith F, Yau S, Simcox EM, Miwa S, Donti T, ... Graham BH, et al. Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. American Journal of Human Genetics. 93: 471-81. PMID 23993193 DOI: 10.1016/j.ajhg.2013.07.017  1
2013 Craigen WJ, Graham BH, Wong LJ, Scaglia F, Lewis RA, Bonnen PE. Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology. Bmc Medical Genetics. 14: 83. PMID 23947751 DOI: 10.1186/1471-2350-14-83  1
2013 Zhang K, Li Z, Jaiswal M, Bayat V, Xiong B, Sandoval H, Charng WL, David G, Haueter C, Yamamoto S, Graham BH, Bellen HJ. The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit. The Journal of Cell Biology. 200: 807-20. PMID 23509070 DOI: 10.1083/Jcb.201208033  1
2013 Tang S, Wang J, Zhang VW, Li FY, Landsverk M, Cui H, Truong CK, Wang G, Chen LC, Graham B, Scaglia F, Schmitt ES, Craigen WJ, Wong LJ. Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects. Human Mutation. 34: 882-93. PMID 23463613 DOI: 10.1002/Humu.22307  1
2013 Bainbridge MN, Hu H, Muzny DM, Musante L, Lupski JR, Graham BH, Chen W, Gripp KW, Jenny K, Wienker TF, Yang Y, Sutton VR, Gibbs RA, Ropers HH. De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine. 5: 11. PMID 23383720 DOI: 10.1186/Gm415  1
2013 Cui H, Li F, Chen D, Wang G, Truong CK, Enns GM, Graham B, Milone M, Landsverk ML, Wang J, Zhang W, Wong LJ. Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 388-94. PMID 23288206 DOI: 10.1038/Gim.2012.144  1
2012 Arnold GL, Salazar D, Neidich JA, Suwannarat P, Graham BH, Lichter-Konecki U, Bosch AM, Cusmano-Ozog K, Enns G, Wright EL, Lanpher BC, Owen NN, Lipson MH, Cerone R, Levy P, et al. Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening. Molecular Genetics and Metabolism. 106: 439-41. PMID 22658692 DOI: 10.1016/j.ymgme.2012.04.006  1
2012 Yeoh JW, James MH, Jobling P, Bains JS, Graham BA, Dayas CV. Cocaine potentiates excitatory drive in the perifornical/lateral hypothalamus. The Journal of Physiology. 590: 3677-89. PMID 22641785 DOI: 10.1113/Jphysiol.2012.230268  1
2012 Kang P, Lee HK, Glasgow SM, Finley M, Donti T, Gaber ZB, Graham BH, Foster AE, Novitch BG, Gronostajski RM, Deneen B. Sox9 and NFIA coordinate a transcriptional regulatory cascade during the initiation of gliogenesis. Neuron. 74: 79-94. PMID 22500632 DOI: 10.1016/J.Neuron.2012.01.024  1
2012 Bayat V, Thiffault I, Jaiswal M, Tétreault M, Donti T, Sasarman F, Bernard G, Demers-Lamarche J, Dicaire MJ, Mathieu J, Vanasse M, Bouchard JP, Rioux MF, Lourenco CM, Li Z, ... Graham BH, et al. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. Plos Biology. 10: e1001288. PMID 22448145 DOI: 10.1371/Journal.Pbio.1001288  1
2012 Wang J, Schmitt ES, Landsverk ML, Zhang VW, Li FY, Graham BH, Craigen WJ, Wong LJ. An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experience. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 620-6. PMID 22402757 DOI: 10.1038/Gim.2012.4  1
2012 Li Z, Graham BH. Measurement of mitochondrial oxygen consumption using a Clark electrode. Methods in Molecular Biology (Clifton, N.J.). 837: 63-72. PMID 22215541 DOI: 10.1007/978-1-61779-504-6_5  1
2012 Graham BH. Diagnostic challenges of mitochondrial disorders: complexities of two genomes. Methods in Molecular Biology (Clifton, N.J.). 837: 35-46. PMID 22215539 DOI: 10.1007/978-1-61779-504-6_3  0.01
2012 Raghavan A, Sheiko T, Graham BH, Craigen WJ. Voltage-dependant anion channels: novel insights into isoform function through genetic models. Biochimica Et Biophysica Acta. 1818: 1477-85. PMID 22051019 DOI: 10.1016/j.bbamem.2011.10.019  1
2012 Nagamani SC, Erez A, Bay C, Pettigrew A, Lalani SR, Herman K, Graham BH, Nowaczyk MJ, Proud M, Craigen WJ, Hopkins B, Kozel B, Plunkett K, Hixson P, Stankiewicz P, et al. Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44. European Journal of Human Genetics : Ejhg. 20: 176-9. PMID 21934713 DOI: 10.1038/Ejhg.2011.171  1
2011 Flynn JR, Brichta AM, Galea MP, Callister RJ, Graham BA. A horizontal slice preparation for examining the functional connectivity of dorsal column fibres in mouse spinal cord. Journal of Neuroscience Methods. 200: 113-20. PMID 21726580 DOI: 10.1016/J.Jneumeth.2011.06.017  1
2011 Pennington PR, Wei Z, Rui L, Doig JA, Graham B, Kuski K, Gabriel GG, Mousseau DD. Alzheimer disease-related presenilin-1 variants exert distinct effects on monoamine oxidase-A activity in vitro. Journal of Neural Transmission (Vienna, Austria : 1996). 118: 987-95. PMID 21373759 DOI: 10.1007/s00702-011-0616-7  0.01
2011 Flynn JR, Graham BA, Galea MP, Callister RJ. The role of propriospinal interneurons in recovery from spinal cord injury. Neuropharmacology. 60: 809-22. PMID 21251920 DOI: 10.1016/J.Neuropharm.2011.01.016  1
2010 Zoccolan D, Graham BJ, Cox DD. A self-calibrating, camera-based eye tracker for the recording of rodent eye movements. Frontiers in Neuroscience. 4: 193. PMID 21152259 DOI: 10.3389/fnins.2010.00193  1
2010 Rea SL, Graham BH, Nakamaru-Ogiso E, Kar A, Falk MJ. Bacteria, yeast, worms, and flies: exploiting simple model organisms to investigate human mitochondrial diseases. Developmental Disabilities Research Reviews. 16: 200-18. PMID 20818735 DOI: 10.1002/ddrr.114  0.01
2010 Callister RJ, Graham BA. Early history of glycine receptor biology in Mammalian spinal cord circuits. Frontiers in Molecular Neuroscience. 3: 13. PMID 20577630 DOI: 10.3389/Fnmol.2010.00013  1
2010 Szafranski P, Schaaf CP, Person RE, Gibson IB, Xia Z, Mahadevan S, Wiszniewska J, Bacino CA, Lalani S, Potocki L, Kang SH, Patel A, Cheung SW, Probst FJ, Graham BH, et al. Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological? Human Mutation. 31: 840-50. PMID 20506139 DOI: 10.1002/Humu.21284  1
2010 de Oliveira RB, Graham B, Howlett MC, Gravina FS, Oliveira MW, Imtiaz MS, Callister RJ, Lim R, Brichta AM, van Helden DF. Ketamine anesthesia helps preserve neuronal viability. Journal of Neuroscience Methods. 189: 230-2. PMID 20380852 DOI: 10.1016/J.Jneumeth.2010.03.029  1
2010 Wong LJ, Scaglia F, Graham BH, Craigen WJ. Current molecular diagnostic algorithm for mitochondrial disorders. Molecular Genetics and Metabolism. 100: 111-7. PMID 20359921 DOI: 10.1016/j.ymgme.2010.02.024  1
2010 Jobling P, Graham BA, Brichta AM, Callister RJ. Cervix stimulation evokes predominantly subthreshold synaptic responses in mouse thoracolumbar and lumbosacral superficial dorsal horn neurons. The Journal of Sexual Medicine. 7: 2068-76. PMID 20345730 DOI: 10.1111/J.1743-6109.2010.01768.X  1
2010 Graham BH, Li Z, Alesii EP, Versteken P, Lee C, Wang J, Craigen WJ. Neurologic dysfunction and male infertility in Drosophila porin mutants: a new model for mitochondrial dysfunction and disease. The Journal of Biological Chemistry. 285: 11143-53. PMID 20110367 DOI: 10.1074/jbc.M109.080317  1
2010 El-Hattab AW, Li FY, Shen J, Powell BR, Bawle EV, Adams DJ, Wahl E, Kobori JA, Graham B, Scaglia F, Wong LJ. Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 19-24. PMID 20027113 DOI: 10.1097/GIM.0b013e3181c5e6f7  1
2010 Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, et al. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. Journal of Medical Genetics. 47: 332-41. PMID 19914906 DOI: 10.1136/Jmg.2009.073015  1
2010 Franco LM, de Ravel T, Graham BH, Frenkel SM, Van Driessche J, Stankiewicz P, Lupski JR, Vermeesch JR, Cheung SW. A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. European Journal of Human Genetics : Ejhg. 18: 258-61. PMID 19844260 DOI: 10.1038/ejhg.2009.164  1
2009 Anderson WB, Graham BA, Beveridge NJ, Tooney PA, Brichta AM, Callister RJ. Different forms of glycine- and GABA(A)-receptor mediated inhibitory synaptic transmission in mouse superficial and deep dorsal horn neurons. Molecular Pain. 5: 65. PMID 19919721 DOI: 10.1186/1744-8069-5-65  1
2009 Li L, Shen JJ, Bournat JC, Huang L, Chattopadhyay A, Li Z, Shaw C, Graham BH, Brown CW. Activin signaling: effects on body composition and mitochondrial energy metabolism. Endocrinology. 150: 3521-9. PMID 19389832 DOI: 10.1210/En.2008-0922  1
2009 Wang J, Brautbar A, Chan AK, Dzwiniel T, Li FY, Waters PJ, Graham BH, Wong LJ. Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family. Molecular Genetics and Metabolism. 96: 59-65. PMID 19062322 DOI: 10.1016/j.ymgme.2008.10.006  1
2009 Ortiz FE, Graham B, Spagnoli K, Kelmelis EJ. Biologically inspired collision avoidance system for unmanned vehicles Proceedings of Spie. 7332. DOI: 10.1117/12.820756  0.01
2008 Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, et al. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nature Genetics. 40: 1466-71. PMID 19029900 DOI: 10.1038/Ng.279  1
2008 Craigen WJ, Graham BH. Genetic strategies for dissecting mammalian and Drosophila voltage-dependent anion channel functions. Journal of Bioenergetics and Biomembranes. 40: 207-12. PMID 18622693 DOI: 10.1007/s10863-008-9146-x  1
2008 Brautbar A, Wang J, Abdenur JE, Chang RC, Thomas JA, Grebe TA, Lim C, Weng SW, Graham BH, Wong LJ. The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle. Molecular Genetics and Metabolism. 94: 485-90. PMID 18495510 DOI: 10.1016/j.ymgme.2008.04.004  1
2007 Brunetti-Pierri N, Mian A, Luetchke R, Graham BH. Intrauterine growth retardation and placental vacuolization as presenting features in a case of GM1 gangliosidosis. Journal of Inherited Metabolic Disease. 30: 823. PMID 17712606 DOI: 10.1007/s10545-007-0628-5  0.01
2007 Holder AM, Graham BH, Lee B, Scott DA. Fine-Lubinsky syndrome: sibling pair suggests possible autosomal recessive inheritance. American Journal of Medical Genetics. Part A. 143: 2576-80. PMID 17394214 DOI: 10.1002/Ajmg.A.31688  1
2007 Sano M, Izumi Y, Helenius K, Asakura M, Rossi DJ, Xie M, Taffet G, Hu L, Pautler RG, Wilson CR, Boudina S, Abel ED, Taegtmeyer H, Scaglia F, Graham BH, et al. Ménage-à-trois 1 is critical for the transcriptional function of PPARgamma coactivator 1. Cell Metabolism. 5: 129-42. PMID 17276355 DOI: 10.1016/J.Cmet.2007.01.003  1
2006 Graham BA, Schofield PR, Sah P, Margrie TW, Callister RJ. Distinct physiological mechanisms underlie altered glycinergic synaptic transmission in the murine mutants spastic, spasmodic, and oscillator. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 4880-90. PMID 16672662 DOI: 10.1523/Jneurosci.3991-05.2006  1
2005 Graham BH, Craigen WJ. Mitochondrial voltage-dependent anion channel gene family in Drosophila melanogaster: complex patterns of evolution, genomic organization, and developmental expression. Molecular Genetics and Metabolism. 85: 308-17. PMID 15886041 DOI: 10.1016/j.ymgme.2005.03.009  1
2004 Graham BH, Craigen WJ. Genetic approaches to analyzing mitochondrial outer membrane permeability. Current Topics in Developmental Biology. 59: 87-118. PMID 14975248 DOI: 10.1016/S0070-2153(04)59004-X  1
2004 Komarov AG, Graham BH, Craigen WJ, Colombini M. The physiological properties of a novel family of VDAC-like proteins from Drosophila melanogaster. Biophysical Journal. 86: 152-62. PMID 14695259 DOI: 10.1016/S0006-3495(04)74093-X  1
2002 Graham BH, David Sweatt J, Craigen WJ. Noninvasive, in vivo approaches to evaluating behavior and exercise physiology in mouse models of mitochondrial disease. Methods (San Diego, Calif.). 26: 364-70. PMID 12054928 DOI: 10.1016/S1046-2023(02)00043-9  1
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