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20042019
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Research Output 2004 2019

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40 Citations (Scopus)

52 Genetic Loci Influencing Myocardial Mass

van der Harst, P., van Setten, J., Verweij, N., Vogler, G., Franke, L., Maurano, M. T., Wang, X., Mateo Leach, I., Eijgelsheim, M., Sotoodehnia, N., Hayward, C., Sorice, R., Meirelles, O., Lyytikäinen, L. P., Polašek, O., Tanaka, T., Arking, D. E., Ulivi, S., Trompet, S., Müller-Nurasyid, M. & 140 others, Smith, A. V., Dörr, M., Kerr, K. F., Magnani, J. W., Del Greco M., F., Zhang, W., Nolte, I. M., Silva, C. T., Padmanabhan, S., Tragante, V., Esko, T., Abecasis, G. R., Adriaens, M. E., Andersen, K., Barnett, P., Bis, J. C., Bodmer, R., Buckley, B. M., Campbell, H., Cannon, M. V., Chakravarti, A., Chen, L. Y., Delitala, A., Devereux, R. B., Doevendans, P. A., Dominiczak, A. F., Ferrucci, L., Ford, I., Gieger, C., Harris, T. B., Haugen, E., Heinig, M., Hernandez, D. G., Hillege, H. L., Hirschhorn, J. N., Hofman, A., Hubner, N., Hwang, S. J., Iorio, A., Kähönen, M., Kellis, M., Kolcic, I., Kooner, I. K., Kooner, J. S., Kors, J. A., Lakatta, E. G., Lage, K., Launer, L. J., Levy, D., Lundby, A., Macfarlane, P. W., May, D., Meitinger, T., Metspalu, A., Nappo, S., Naitza, S., Neph, S., Nord, A., Nutile, T., Okin, P. M., Olsen, J. V., Oostra, B. A., Penninger, J. M., Pennacchio, L. A., Pers, T. H., Perz, S., Peters, A., Pinto, Y. M., Pfeufer, A., Pilia, M. G., Pramstaller, P. P., Prins, B. P., Raitakari, O. T., Raychaudhuri, S., Rice, K. M., Rossin, E. J., Rotter, J. I., Schafer, S., Schlessinger, D., Schmidt, C. O., Sehmi, J., Silljé, H. H. W., Sinagra, G., Sinner, M. F., Slowikowski, K., Soliman, E. Z., Spector, T. D., Spiering, W., Stamatoyannopoulos, J. A., Stolk, R. P., Strauch, K., Tan, S. T., Tarasov, K. V., Trinh, B., Uitterlinden, A. G., van den Boogaard, M., van Duijn, C. M., van Gilst, W. H., Viikari, J. S., Visscher, P. M., Vitart, V., Völker, U., Waldenberger, M., Weichenberger, C. X., Westra, H. J., Wijmenga, C., Wolffenbuttel, B. H., Yang, J., Bezzina, C. R., Munroe, P. B., Snieder, H., Wright, A. F., Rudan, I., Boyer, L. A., Asselbergs, F. W., van Veldhuisen, D. J., Stricker, B. H., Psaty, B. M., Ciullo, M., Sanna, S., Lehtimäki, T., Wilson, J. F., Bandinelli, S., Alonso, A., Gasparini, P., Jukema, J. W., Kääb, S., Gudnason, V., Felix, S. B., Heckbert, S. R., de Boer, R. A., Newton-Cheh, C., Hicks, A. A., Chambers, J. C., Jamshidi, Y., Visel, A., Christoffels, V. M., Isaacs, A., Samani, N. J. & de Bakker, P. I. W., Sep 27 2016, In : Journal of the American College of Cardiology. 68, 13, p. 1435-1448 14 p.

Research output: Contribution to journalArticle

Genetic Loci
Cardiomegaly
Meta-Analysis
Myocardium
Histone Code
112 Citations (Scopus)

Accurate and exact CNV identification from targeted high-throughput sequence data

Nord, A., Lee, M., King, M. C. & Walsh, T., Apr 12 2011, In : BMC Genomics. 12, 184.

Research output: Contribution to journalArticle

High-Throughput Nucleotide Sequencing
Mutation
Nucleotides
Technology
DNA
19 Citations (Scopus)

A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk

Crawford, D. C., Nord, A., Badzioch, M. D., Ranchalis, J., McKinstry, L. A., Ahearn, M., Bertucci, C., Shephard, C., Wong, M., Rieder, M. J., Schellenberg, G. D., Nickerson, D. A., Heagerty, P. J., Wijsman, E. M. & Jarvik, G. P., Mar 1 2008, In : Journal of Lipid Research. 49, 3, p. 588-596 9 p.

Research output: Contribution to journalArticle

Carotid Artery Diseases
Polymorphism
Genotype
Single Nucleotide Polymorphism
Body Mass Index
133 Citations (Scopus)

A high-resolution enhancer atlas of the developing telencephalon

Visel, A., Taher, L., Girgis, H., May, D., Golonzhka, O., Hoch, R. V., McKinsey, G. L., Pattabiraman, K., Silberberg, S. N., Blow, M. J., Hansen, D. V., Nord, A., Akiyama, J. A., Holt, A., Hosseini, R., Phouanenavong, S., Plajzer-Frick, I., Shoukry, M., Afzal, V., Kaplan, T. & 5 others, Kriegstein, A. R., Rubin, E. M., Ovcharenko, I., Pennacchio, L. A. & Rubenstein, J. L. R., Feb 14 2013, In : Cell. 152, 4, p. 895-908 14 p.

Research output: Contribution to journalArticle

Telencephalon
Atlases
Genes
Prosencephalon
Regulator Genes
53 Citations (Scopus)

Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgery

Gaynor, J. W., Nord, A., Wernovsky, G., Bernbaum, J., Solot, C. B., Burnham, N., Zackai, E., Heagerty, P. J., Clancy, R. R., Nicolson, S. C., Jarvik, G. P. & Gerdes, M., Jul 1 2009, In : Pediatrics. 124, 1, p. 241-250 10 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Risk-Taking
Thoracic Surgery
Congenital Heart Defects
Alleles
135 Citations (Scopus)

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing

Pritchard, C. C., Smith, C., Salipante, S. J., Lee, M. K., Thornton, A. M., Nord, A., Gulden, C., Kupfer, S. S., Swisher, E. M., Bennett, R. L., Novetsky, A. P., Jarvik, G. P., Olopade, O. I., Goodfellow, P. J., King, M. C., Tait, J. F. & Walsh, T., Jul 1 2012, In : Journal of Molecular Diagnostics. 14, 4, p. 357-366 10 p.

Research output: Contribution to journalArticle

Hereditary Nonpolyposis Colorectal Neoplasms
High-Throughput Nucleotide Sequencing
Mutation
Genetic Testing
Genes
1 Citation (Scopus)

Common CHD8 genomic targets contrast with model-specific transcriptional impacts of CHD8 haploinsufficiency

Wade, A. A., Lim, K., Catta-Preta, R. & Nord, A., Jan 7 2019, In : Frontiers in Molecular Neuroscience. 11, 481.

Research output: Contribution to journalArticle

Open Access
Haploinsufficiency
DNA-Binding Proteins
Genes
Chromatin
Chromatin Assembly and Disassembly
21 Citations (Scopus)

Congenital Heart Defects in Patients with Deletions Upstream of SOX9

Sanchez-Castro, M., Gordon, C. T., Petit, F., Nord, A., Callier, P., Andrieux, J., Guérin, P., Pichon, O., David, A., Abadie, V., Bonnet, D., Visel, A., Pennacchio, L. A., Amiel, J., Lyonnet, S. & Le Caignec, C., Dec 1 2013, In : Human Mutation. 34, 12, p. 1628-1631 4 p.

Research output: Contribution to journalArticle

Pierre Robin Syndrome
Congenital Heart Defects
SOX9 Transcription Factor
Campomelic Dysplasia
Disorders of Sex Development
326 Citations (Scopus)

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Walsh, T., Lee, M. K., Casadei, S., Thornton, A. M., Stray, S. M., Pennil, C., Nord, A., Mandell, J. B., Swisher, E. M. & King, M. C., Jul 13 2010, In : Proceedings of the National Academy of Sciences of the United States of America. 107, 28, p. 12629-12633 5 p.

Research output: Contribution to journalArticle

High-Throughput Nucleotide Sequencing
Ovarian Neoplasms
Breast Neoplasms
Mutation
Genetic Testing
6 Citations (Scopus)

Dlx1 and Dlx2 Promote Interneuron GABA Synthesis, Synaptogenesis, and Dendritogenesis

Pla, R., Stanco, A., Howard, M. A., Rubin, A. N., Vogt, D., Mortimer, N., Cobos, I., Potter, G. B., Lindtner, S., Price, J. D., Nord, A., Visel, A., Schreiner, C. E., Baraban, S. C., Rowitch, D. H. & Rubenstein, J. L. R., Nov 1 2018, In : Cerebral cortex (New York, N.Y. : 1991). 28, 11, p. 3797-3815 19 p.

Research output: Contribution to journalArticle

Interneurons
gamma-Aminobutyric Acid
Synapses
Autistic Disorder
Dendrites
124 Citations (Scopus)

Fine tuning of craniofacial morphology by distant-acting enhancers

Attanasio, C., Nord, A., Zhu, Y., Blow, M. J., Li, Z., Liberton, D. K., Morrison, H., Plajzer-Frick, I., Holt, A., Hosseini, R., Phouanenavong, S., Akiyama, J. A., Shoukry, M., Afzal, V., Rubin, E. M., FitzPatrick, D. R., Ren, B., Hallgrímsson, B., Pennacchio, L. A. & Visel, A., Jan 1 2013, In : Science. 342, 6157, 1241006.

Research output: Contribution to journalArticle

Skull
Regulator Genes
Epigenomics
Transgenic Mice
Proteins
59 Citations (Scopus)

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

Shahin, H., Walsh, T., Rayyan, A. A., Lee, M. K., Higgins, J., Dickel, D., Lewis, K., Thompson, J., Baker, C., Nord, A., Stray, S., Gurwitz, D., Avraham, K. B., King, M. C. & Kanaan, M., Apr 1 2010, In : European Journal of Human Genetics. 18, 4, p. 407-413 7 p.

Research output: Contribution to journalArticle

Hearing Loss
Single Nucleotide Polymorphism
Nuclear Family
Siblings
Parents
25 Citations (Scopus)

Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia

Rippey, C., Walsh, T., Gulsuner, S., Brodsky, M., Nord, A., Gasperini, M., Pierce, S., Spurrell, C., Coe, B. P., Krumm, N., Lee, M. K., Sebat, J., McClellan, J. M. & King, M. C., Oct 3 2013, In : American Journal of Human Genetics. 93, 4, p. 697-710 14 p.

Research output: Contribution to journalArticle

Gene Dosage
Schizophrenia
Genes
Neuronal Plasticity
Brain
48 Citations (Scopus)

Function-based identification of mammalian enhancers using site-specific integration

Dickel, D. E., Zhu, Y., Nord, A., Wylie, J. N., Akiyama, J. A., Afzal, V., Plajzer-Frick, I., Kirkpatrick, A., Göttgens, B., Bruneau, B. G., Visel, A. & Pennacchio, L. A., Jan 1 2014, In : Nature Methods. 11, 5, p. 566-571 6 p.

Research output: Contribution to journalArticle

Sorting
Assays
Flow Cytometry
Throughput
High-Throughput Nucleotide Sequencing
47 Citations (Scopus)

Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot

Zeltser, I., Jarvik, G. P., Bernbaum, J., Wernovsky, G., Nord, A., Gerdes, M., Zackai, E., Clancy, R., Nicolson, S. C., Spray, T. L. & Gaynor, J. W., Jan 1 2008, In : Journal of Thoracic and Cardiovascular Surgery. 135, 1, p. 91-97 7 p.

Research output: Contribution to journalArticle

Tetralogy of Fallot
Apolipoprotein E2
Alleles
Pulmonary Atresia
Congenital Heart Defects
24 Citations (Scopus)

Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk

Ronald, J., Rajagopalan, R., Cerrato, F., Nord, A., Hatsukami, T., Kohler, T., Marcovina, S., Heagerty, P. & Jarvik, G. P., Jan 1 2011, In : Stroke. 42, 1, p. 2-9 8 p.

Research output: Contribution to journalArticle

Lipoprotein(a)
Carotid Artery Diseases
Kringles
Single Nucleotide Polymorphism
Alleles
63 Citations (Scopus)

Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q

Ober, C., Nord, A., Thompson, E. E., Pan, L., Tan, Z., Cusanovich, D., Sun, Y., Nicolae, R., Edelstein, C., Schneider, D. H., Billstrand, C., Pfaffinger, D., Phillips, N., Anderson, R. L., Philips, B., Rajagopalan, R., Hatsukami, T. S., Rieder, M. J., Heagerty, P. J., Nickerson, D. A. & 5 others, Abney, M., Marcovina, S., Jarvik, G. P., Scanu, A. M. & Nicolae, D. L., May 1 2009, In : Journal of Lipid Research. 50, 5, p. 798-806 9 p.

Research output: Contribution to journalArticle

Lipoprotein(a)
Genome-Wide Association Study
Chromosomes
Genes
Kringles
2 Citations (Scopus)

Genomic analysis of transcriptional networks directing progression of cell states during MGE development 06 Biological Sciences 0604 Genetics

Sandberg, M., Taher, L., Hu, J., Black, B. L., Nord, A. & Rubenstein, J. L. R., Sep 14 2018, In : Neural Development. 13, 1, 21.

Research output: Contribution to journalArticle

Median Eminence
Biological Science Disciplines
Gene Regulatory Networks
Transcription Factors
GABAergic Neurons
60 Citations (Scopus)

Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51

Walsh, T., Pierce, S. B., Lenz, D. R., Brownstein, Z., Dagan-Rosenfeld, O., Shahin, H., Roeb, W., McCarthy, S., Nord, A., Gordon, C. R., Ben-Neriah, Z., Sebat, J., Kanaan, M., Lee, M. K., Frydman, M., King, M. C. & Avraham, K. B., Jul 9 2010, In : American Journal of Human Genetics. 87, 1, p. 101-109 9 p.

Research output: Contribution to journalArticle

Hearing Loss
Apoptosis
Gene Expression
Inner Ear
Glycogen Synthase Kinase 3

Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons

Lindtner, S., Catta-Preta, R., Tian, H., Su-Feher, L., Price, J. D., Dickel, D. E., Greiner, V., Silberberg, S. N., McKinsey, G. L., McManus, M. T., Pennacchio, L. A., Visel, A., Nord, A. & Rubenstein, J. L. R., Jan 1 2019, (Accepted/In press) In : Cell Reports.

Research output: Contribution to journalArticle

Open Access
GABAergic Neurons
Prosencephalon
Neurons
Transcription Factors
Epigenomics
340 Citations (Scopus)

Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas

Pennington, K. P., Walsh, T., Harrell, M. I., Lee, M. K., Pennil, C. C., Rendi, M. H., Thornton, A., Norquist, B. M., Casadei, S., Nord, A., Agnew, K. J., Pritchard, C. C., Scroggins, S., Garcia, R. L., King, M. C. & Swisher, E. M., Feb 11 2014, In : Clinical Cancer Research. 20, 3, p. 764-775 12 p.

Research output: Contribution to journalArticle

Fallopian Tubes
Germ-Line Mutation
Homologous Recombination
Platinum
Carcinoma
50 Citations (Scopus)

Germline Chd8 haploinsufficiency alters brain development in mouse

Gompers, A. L., Su-Feher, L., Ellegood, J., Copping, N. A., Riyadh, M. A., Stradleigh, T. W., Pride, M. C., Schaffler, M. D., Wade, A. A., Catta-Preta, R., Zdilar, I., Louis, S., Kaushik, G., Mannion, B. J., Plajzer-Frick, I., Afzal, V., Visel, A., Pennacchio, L. A., Dickel, D. E., Lerch, J. P. & 4 others, Crawley, J., Zarbalis, K., Silverman, J. L. & Nord, A., Aug 1 2017, In : Nature Neuroscience. 20, 8, p. 1062-1073 12 p.

Research output: Contribution to journalArticle

Haploinsufficiency
Brain
Chromatin Assembly and Disassembly
Neuroimmunomodulation
cdc Genes
58 Citations (Scopus)

Is cardiac diagnosis a predictor of neurodevelopmental outcome after cardiac surgery in infancy?

Gaynor, J. W., Gerdes, M., Nord, A., Bernbaum, J., Zackai, E., Wernovsky, G., Clancy, R. R., Heagerty, P. J., Solot, C. B., McDonald-Mcginn, D. & Jarvik, G. P., Dec 1 2010, In : Journal of Thoracic and Cardiovascular Surgery. 140, 6, p. 1230-1236 7 p.

Research output: Contribution to journalArticle

Hypoplastic Left Heart Syndrome
Thoracic Surgery
Transposition of Great Vessels
Tetralogy of Fallot
Ventricular Heart Septal Defects
10 Citations (Scopus)

Modeling insertional mutagenesis using gene length and expression in murine embryonic stem cells

Nord, A., Vranizan, K., Tingley, W., Zambon, A. C., Hanspers, K., Fong, L. G., Hu, Y., Bacchetti, P., Ferrin, T. E., Babbitt, P. C., Doniger, S. W., Skarnes, W. C., Young, S. G. & Conklin, B. R., Jul 18 2007, In : PLoS One. 2, 7, e617.

Research output: Contribution to journalArticle

insertional mutagenesis
Mutagenesis
Insertional Mutagenesis
embryonic stem cells
Embryonic Stem Cells
485 Citations (Scopus)

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

Walsh, T., Casadei, S., Lee, M. K., Pennil, C. C., Nord, A., Thornton, A. M., Roeb, W., Agnew, K. J., Stray, S. M., Wickramanayake, A., Norquist, B., Pennington, K. P., Garcia, R. L., King, M. C. & Swisher, E. M., Nov 1 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 44, p. 18032-18037 6 p.

Research output: Contribution to journalArticle

High-Throughput Nucleotide Sequencing
Fallopian Tubes
Carcinoma
Mutation
Genes
5 Citations (Scopus)

Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity

Fazel Darbandi, S., Robinson Schwartz, S. E., Qi, Q., Catta-Preta, R., Pai, E. L. L., Mandell, J. D., Everitt, A., Rubin, A., Krasnoff, R. A., Katzman, S., Tastad, D., Nord, A., Willsey, A. J., Chen, B., State, M. W., Sohal, V. S. & Rubenstein, J. L. R., Nov 21 2018, In : Neuron. 100, 4, p. 831-845 15 p.

Research output: Contribution to journalArticle

Heterozygote
Neurons
RNA Sequence Analysis
Phenotype
Cell Physiological Phenomena
128 Citations (Scopus)

Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndrome

Tabbutt, S., Nord, A., Jarvik, G. P., Bernbaum, J., Wernovsky, G., Gerdes, M., Zackai, E., Clancy, R. R., Nicolson, S. C., Spray, T. L. & Gaynor, J. W., Mar 1 2008, In : Pediatrics. 121, 3, p. 476-483 8 p.

Research output: Contribution to journalArticle

Hypoplastic Left Heart Syndrome
Deep Hypothermia Induced Circulatory Arrest
Extracorporeal Membrane Oxygenation
Disabled Children
Child Development
173 Citations (Scopus)

Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery

Gaynor, J. W., Wernovsky, G., Jarvik, G. P., Bernbaum, J., Gerdes, M., Zackai, E., Nord, A., Clancy, R. R., Nicolson, S. C. & Spray, T. L., May 1 2007, In : Journal of Thoracic and Cardiovascular Surgery. 133, 5

Research output: Contribution to journalArticle

Deep Hypothermia Induced Circulatory Arrest
Thoracic Surgery
Apolipoprotein E2
Cardiopulmonary Bypass
Alleles
23 Citations (Scopus)

Pbx Regulates Patterning of the Cerebral Cortex in Progenitors and Postmitotic Neurons

Golonzhka, O., Nord, A., Tang, P. L. F., Lindtner, S., Ypsilanti, A. R., Ferretti, E., Visel, A., Selleri, L. & Rubenstein, J. L. R., Jan 1 2015, In : Neuron. 88, 6, p. 1192-1207 16 p.

Research output: Contribution to journalArticle

Frontal Lobe
Cerebral Cortex
Neurons
Neocortex
Mutagenesis
76 Citations (Scopus)

Perioperative Stroke in Infants Undergoing Open Heart Operations for Congenital Heart Disease

Chen, J., Zimmerman, R. A., Jarvik, G. P., Nord, A., Clancy, R. R., Wernovsky, G., Montenegro, L. M., Hartman, D. M., Nicolson, S. C., Spray, T. L., Gaynor, J. W. & Ichord, R., Sep 1 2009, In : Annals of Thoracic Surgery. 88, 3, p. 823-829 7 p.

Research output: Contribution to journalArticle

Heart Diseases
Stroke
Deep Hypothermia Induced Circulatory Arrest
Cardiopulmonary Bypass
Magnetic Resonance Imaging
65 Citations (Scopus)

Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation

Reiner, A. P., Wurfel, M. M., Lange, L. A., Carlson, C. S., Nord, A., Carty, C. L., Rieder, M. J., Desmarais, C., Jenny, N. S., Iribarren, C., Walston, J. D., Williams, O. D., Nickerson, D. A. & Jarvik, G. P., Jul 1 2008, In : Arteriosclerosis, Thrombosis, and Vascular Biology. 28, 7, p. 1407-1412 6 p.

Research output: Contribution to journalArticle

Interleukin-1 Receptors
Alleles
Inflammation
C-Reactive Protein
Acute-Phase Proteins
74 Citations (Scopus)

Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery

Fuller, S., Nord, A., Gerdes, M., Wernovsky, G., Jarvik, G. P., Bernbaum, J., Zackai, E. & Gaynor, J. W., Jul 1 2009, In : European Journal of Cardio-thoracic Surgery. 36, 1, p. 40-48 9 p.

Research output: Contribution to journalArticle

Thoracic Surgery
Congenital Heart Defects
Birth Weight
Deep Hypothermia Induced Circulatory Arrest
Apolipoprotein E2
163 Citations (Scopus)

Rapid and pervasive changes in genome-wide enhancer usage during mammalian development

Nord, A., Blow, M. J., Attanasio, C., Akiyama, J. A., Holt, A., Hosseini, R., Phouanenavong, S., Plajzer-Frick, I., Shoukry, M., Afzal, V., Rubenstein, J. L. R., Rubin, E. M., Pennacchio, L. A. & Visel, A., Dec 19 2013, In : Cell. 155, 7, p. 1521-1531 11 p.

Research output: Contribution to journalArticle

Genes
Genome
Tissue
Epigenomics
Gene expression
1293 Citations (Scopus)

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

Walsh, T., McClellan, J. M., McCarthy, S. E., Addington, A. M., Pierce, S. B., Cooper, G. M., Nord, A., Kusenda, M., Malhotra, D., Bhandari, A., Stray, S. M., Rippey, C. F., Roccanova, P., Makarov, V., Lakshmi, B., Findling, R. L., Sikich, L., Stromberg, T., Merriman, B., Gogtay, N. & 16 others, Butler, P., Eckstrand, K., Noory, L., Gochman, P., Long, R., Chen, Z., Davis, S., Baker, C., Eichler, E. E., Meltzer, P. S., Nelson, S. F., Singleton, A. B., Lee, M. K., Rapoport, J. L., King, M. C. & Sebat, J., Apr 25 2008, In : Science. 320, 5875, p. 539-543 5 p.

Research output: Contribution to journalArticle

Schizophrenia
Childhood Schizophrenia
Neuregulins
Genes
Mutation
64 Citations (Scopus)

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

Nord, A., Roeb, W., Dickel, D. E., Walsh, T., Kusenda, M., O'Connor, K. L., Malhotra, D., McCarthy, S. E., Stray, S. M., Taylor, S. M., Sebat, J., King, B., King, M. C. & McClellan, J. M., Jun 1 2011, In : European Journal of Human Genetics. 19, 6, p. 727-731 5 p.

Research output: Contribution to journalArticle

Autistic Disorder
Gene Expression
Genes
Comparative Genomic Hybridization
Gene Dosage
38 Citations (Scopus)

Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

Yan, D., Tekin, D., Bademci, G., Foster, J., Cengiz, F. B., Kannan-Sundhari, A., Guo, S., Mittal, R., Zou, B., Grati, M., Kabahuma, R. I., Kameswaran, M., Lasisi, T. J., Adedeji, W. A., Lasisi, A. O., Menendez, I., Herrera, M., Carranza, C., Maroofian, R., Crosby, A. H. & 11 others, Bensaid, M., Masmoudi, S., Behnam, M., Mojarrad, M., Feng, Y., Duman, D., Mawla, A. M., Nord, A., Blanton, S. H., Liu, X. Z. & Tekin, M., Aug 1 2016, In : Human Genetics. 135, 8, p. 953-961 9 p.

Research output: Contribution to journalArticle

Deafness
DNA
Guatemala
Genes
Iran
19 Citations (Scopus)

Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate

Silberberg, S. N., Taher, L., Lindtner, S., Sandberg, M., Nord, A., Vogt, D., Mckinsey, G. L., Hoch, R., Pattabiraman, K., Zhang, D., Ferran, J. L., Rajkovic, A., Golonzhka, O., Kim, C., Zeng, H., Puelles, L., Visel, A. & Rubenstein, J. L. R., Oct 5 2016, In : Neuron. 92, 1, p. 59-74 16 p.

Research output: Contribution to journalArticle

Prosencephalon
Amygdala
Basal Ganglia
Transgenic Mice
Transcription Factors
14 Citations (Scopus)

TagSNP evaluation for the association of 42 inflammation loci and vascular disease: Evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects

Carlson, C. S., Heagerty, P. J., Nord, A., Pritchard, D. K., Ranchalis, J., Boguch, J. M., Duan, H., Hatsukami, T. S., Schwartz, S. M., Rieder, M. J., Nickerson, D. A. & Jarvik, G. P., Mar 1 2007, In : Human Genetics. 121, 1, p. 65-75 11 p.

Research output: Contribution to journalArticle

Carotid Artery Diseases
Vascular Diseases
Interleukin-6
Inflammation
Single Nucleotide Polymorphism
52 Citations (Scopus)

Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy

Kodera, H., Kato, M., Nord, A., Walsh, T., Lee, M., Yamanaka, G., Tohyama, J., Nakamura, K., Nakagawa, E., Ikeda, T., Ben-Zeev, B., Lev, D., Lerman-Sagie, T., Straussberg, R., Tanabe, S., Ueda, K., Amamoto, M., Ohta, S., Nonoda, Y., Nishiyama, K. & 7 others, Tsurusaki, Y., Nakashima, M., Miyake, N., Hayasaka, K., King, M. C., Matsumoto, N. & Saitsu, H., Jul 1 2013, In : Epilepsia. 54, 7, p. 1262-1269 8 p.

Research output: Contribution to journalArticle

Brain Diseases
Mutation
Point Mutation
Genes
RNA Probes
112 Citations (Scopus)

The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse.

Nord, A., Chang, P. J., Conklin, B. R., Cox, A. V., Harper, C. A., Hicks, G. G., Huang, C. C., Johns, S. J., Kawamoto, M., Liu, S., Meng, E. C., Morris, J. H., Rossant, J., Ruiz, P., Skarnes, W. C., Soriano, P., Stanford, W. L., Stryke, D., von Melchner, H., Wurst, W. & 4 others, Yamamura, K. I., Young, S. G., Babbitt, P. C. & Ferrin, T. E., Jan 1 2006, In : Nucleic acids research.. 34, Database issue

Research output: Contribution to journalArticle

Cell Line
Genes
Embryonic Stem Cells
Computational Biology
Mutant Strains Mice
50 Citations (Scopus)

Tissue-Specific RNA Expression Marks Distant-Acting Developmental Enhancers

Wu, H., Nord, A., Akiyama, J. A., Shoukry, M., Afzal, V., Rubin, E. M., Pennacchio, L. A. & Visel, A., Jan 1 2014, In : PLoS Genetics. 10, 9

Research output: Contribution to journalArticle

RNA
tissues
tissue
RNA Sequence Analysis
High-Throughput Nucleotide Sequencing
32 Citations (Scopus)

Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis

Attanasio, C., Nord, A., Zhu, Y., Blow, M. J., Biddie, S. C., Mendenhall, E. M., Dixon, J., Wright, C., Hosseini, R., Akiyama, J. A., Holt, A., Plajzer-Frick, I., Shoukry, M., Afzal, V., Ren, B., Bernstein, B. E., Rubin, E. M., Visel, A. & Pennacchio, L. A., Jan 1 2014, In : Genome Research. 24, 6, p. 920-929 10 p.

Research output: Contribution to journalArticle

Embryonic Development
Chromatin
Histone Code
Rhombencephalon
Neural Tube
29 Citations (Scopus)

Transcriptional Networks Controlled by NKX2-1 in the Development of Forebrain GABAergic Neurons

Sandberg, M., Flandin, P., Silberberg, S., Su-Feher, L., Price, J. D., Hu, J. S., Kim, C., Visel, A., Nord, A. & Rubenstein, J. L. R., Sep 21 2016, In : Neuron. 91, 6, p. 1260-1275 16 p.

Research output: Contribution to journalArticle

GABAergic Neurons
Gene Regulatory Networks
Interneurons
Prosencephalon
Chromatin
39 Citations (Scopus)

Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortex

Pattabiraman, K., Golonzhka, O., Lindtner, S., Nord, A., Taher, L., Hoch, R., Silberberg, S. N., Zhang, D., Chen, B., Zeng, H. K., Pennacchio, L. A., Puelles, L., Visel, A. & Rubenstein, J. L. R., Jun 4 2014, In : Neuron. 82, 5, p. 989-1003 15 p.

Research output: Contribution to journalArticle

Cerebral Cortex
Transcription Factors
Informatics
Brain Diseases
Transgenic Mice