| Year |
Citation |
Score |
| 2019 |
Wang F, Robinson L, Kramer Y, Kalmbach K, Navarro PA, Pimentel R, Pan XV, Weissman S, Liu L, Keefe D. Measurement of Short Telomere Load in Individual Cells International Journal of Genetics. 7: 60. DOI: 10.11648/J.Ijgg.20190703.14 |
0.32 |
|
| 2018 |
Zhang X, Zhang Y, Zhu X, Purmann C, Haney MS, Ward T, Khechaduri A, Yao J, Weissman SM, Urban AE. Local and global chromatin interactions are altered by large genomic deletions associated with human brain development. Nature Communications. 9: 5356. PMID 30559385 DOI: 10.1038/S41467-018-07766-X |
0.629 |
|
| 2017 |
Abyzov A, Tomasini L, Zhou B, Vasmatzis N, Coppola G, Amenduni M, Pattni R, Wilson M, Gerstein M, Weissman S, Urban AE, Vaccarino FM. One thousand somatic SNVs per skin fibroblast cell set baseline of mosaic mutational load with patterns that suggest proliferative origin. Genome Research. PMID 28235832 DOI: 10.1101/Gr.215517.116 |
0.603 |
|
| 2017 |
Scuderi S, Amiri A, Coppola G, Wu F, Franjic D, Sestan N, Gerstein M, Weissman S, Abyzov A, Vaccarino FM. Comparative transcriptome and gene regulation in human iPSC-derived organoids and donor-identical brain tissue Italian Journal of Anatomy and Embryology. 122: 196. DOI: 10.13128/Ijae-21588 |
0.351 |
|
| 2015 |
Akbarian S, Liu C, Knowles JA, Vaccarino FM, Farnham PJ, Crawford GE, Jaffe AE, Pinto D, Dracheva S, Geschwind DH, Mill J, Nairn AC, Abyzov A, Pochareddy S, Prabhakar S, ... Weissman S, et al. The PsychENCODE project. Nature Neuroscience. 18: 1707-1712. PMID 26605881 DOI: 10.1038/Nn.4156 |
0.611 |
|
| 2015 |
Rivera-Mulia JC, Buckley Q, Sasaki T, Zimmerman J, Didier RA, Nazor K, Loring JF, Lian Z, Weissman SM, Robins AJ, Schulz TC, Menendez L, Kulik MJ, Dalton S, Gabr H, et al. Dynamic changes in replication timing and gene expression during lineage specification of human pluripotent stem cells. Genome Research. PMID 26055160 DOI: 10.1101/Gr.187989.114 |
0.307 |
|
| 2014 |
Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, ... ... Weissman SM, et al. A comparative encyclopedia of DNA elements in the mouse genome. Nature. 515: 355-64. PMID 25409824 DOI: 10.1038/Nature13992 |
0.381 |
|
| 2014 |
Han L, Zi X, Garmire LX, Wu Y, Weissman SM, Pan X, Fan R. Co-detection and sequencing of genes and transcripts from the same single cells facilitated by a microfluidics platform. Scientific Reports. 4: 6485. PMID 25255798 DOI: 10.1038/Srep06485 |
0.32 |
|
| 2013 |
Liu L, Karmakar S, Dhar R, Mahajan M, Choudhury A, Weissman S, Pace BS. Regulation of Gγ-globin gene by ATF2 and its associated proteins through the cAMP-response element. Plos One. 8: e78253. PMID 24223142 DOI: 10.1371/Journal.Pone.0078253 |
0.338 |
|
| 2013 |
Zhang Y, Schulz VP, Reed BD, Wang Z, Pan X, Mariani J, Euskirchen G, Snyder MP, Vaccarino FM, Ivanova N, Weissman SM, Szekely AM. Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration. Proceedings of the National Academy of Sciences of the United States of America. 110: 12361-6. PMID 23836664 DOI: 10.1073/Pnas.1309725110 |
0.59 |
|
| 2013 |
Zhang Y, Haraksingh R, Grubert F, Abyzov A, Gerstein M, Weissman S, Urban AE. Child development and structural variation in the human genome. Child Development. 84: 34-48. PMID 23311762 DOI: 10.1111/Cdev.12051 |
0.627 |
|
| 2012 |
Abyzov A, Mariani J, Palejev D, Zhang Y, Haney MS, Tomasini L, Ferrandino AF, Rosenberg Belmaker LA, Szekely A, Wilson M, Kocabas A, Calixto NE, Grigorenko EL, Huttner A, Chawarska K, ... Weissman S, et al. Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells. Nature. 492: 438-42. PMID 23160490 DOI: 10.1038/Nature11629 |
0.618 |
|
| 2012 |
O'Huallachain M, Karczewski KJ, Weissman SM, Urban AE, Snyder MP. Extensive genetic variation in somatic human tissues. Proceedings of the National Academy of Sciences of the United States of America. 109: 18018-23. PMID 23043118 DOI: 10.1073/Pnas.1213736109 |
0.576 |
|
| 2012 |
Charos AE, Reed BD, Raha D, Szekely AM, Weissman SM, Snyder M. A highly integrated and complex PPARGC1A transcription factor binding network in HepG2 cells. Genome Research. 22: 1668-79. PMID 22955979 DOI: 10.1101/Gr.127761.111 |
0.608 |
|
| 2012 |
Gerstein MB, Kundaje A, Hariharan M, Landt SG, Yan KK, Cheng C, Mu XJ, Khurana E, Rozowsky J, Alexander R, Min R, Alves P, Abyzov A, Addleman N, Bhardwaj N, ... ... Weissman SM, et al. Architecture of the human regulatory network derived from ENCODE data. Nature. 489: 91-100. PMID 22955619 DOI: 10.1038/Nature11245 |
0.758 |
|
| 2012 |
Stamatoyannopoulos JA, Snyder M, Hardison R, Ren B, Gingeras T, Gilbert DM, Groudine M, Bender M, Kaul R, Canfield T, Giste E, Johnson A, Zhang M, Balasundaram G, ... ... Weissman SM, et al. An encyclopedia of mouse DNA elements (Mouse ENCODE). Genome Biology. 13: 418. PMID 22889292 DOI: 10.1186/Gb-2012-13-8-418 |
0.602 |
|
| 2012 |
Wu JQ, Seay M, Schulz VP, Hariharan M, Tuck D, Lian J, Du J, Shi M, Ye Z, Gerstein M, Snyder MP, Weissman S. Tcf7 is an important regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell line. Plos Genetics. 8: e1002565. PMID 22412390 DOI: 10.1371/Journal.Pgen.1002565 |
0.304 |
|
| 2012 |
Szekely A, Zhang Y, Reed B, Schulz V, Wang Z, Euskirchen G, Snyder M, Ivanova N, Weissman S. Pooled Short Hairpin (shRNA) Library Screen Coupled with Next-Generation Sequencing Efficiently Uncover Transcriptional Network in Neural Lineage Development of Human Embryonic Stem Cells (IN8-1.009) Neurology. 78: IN8-1.009-IN8-1.009. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In8-1.009 |
0.633 |
|
| 2011 |
Wontakal SN, Guo X, Will B, Shi M, Raha D, Mahajan MC, Weissman S, Snyder M, Steidl U, Zheng D, Skoultchi AI. A large gene network in immature erythroid cells is controlled by the myeloid and B cell transcriptional regulator PU.1. Plos Genetics. 7: e1001392. PMID 21695229 DOI: 10.1371/Journal.Pgen.1001392 |
0.348 |
|
| 2011 |
Vaccarino FM, Stevens HE, Kocabas A, Palejev D, Szekely A, Grigorenko EL, Weissman S. Induced pluripotent stem cells: a new tool to confront the challenge of neuropsychiatric disorders. Neuropharmacology. 60: 1355-63. PMID 21371482 DOI: 10.1016/J.Neuropharm.2011.02.021 |
0.318 |
|
| 2011 |
Vaccarino FM, Urban AE, Stevens HE, Szekely A, Abyzov A, Grigorenko EL, Gerstein M, Weissman S. Annual Research Review: The promise of stem cell research for neuropsychiatric disorders. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 52: 504-16. PMID 21204834 DOI: 10.1111/J.1469-7610.2010.02348.X |
0.56 |
|
| 2010 |
Kasowski M, Grubert F, Heffelfinger C, Hariharan M, Asabere A, Waszak SM, Habegger L, Rozowsky J, Shi M, Urban AE, Hong MY, Karczewski KJ, Huber W, Weissman SM, Gerstein MB, et al. Variation in transcription factor binding among humans. Science (New York, N.Y.). 328: 232-5. PMID 20299548 DOI: 10.1126/science.1183621 |
0.76 |
|
| 2010 |
Wu JQ, Habegger L, Noisa P, Szekely A, Qiu C, Hutchison S, Raha D, Egholm M, Lin H, Weissman S, Cui W, Gerstein M, Snyder M. Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing. Proceedings of the National Academy of Sciences of the United States of America. 107: 5254-9. PMID 20194744 DOI: 10.1073/Pnas.0914114107 |
0.321 |
|
| 2010 |
Lian Z, Mahajan M, Schulz V, Gulcicek E, Krause D, Weissman SM. Intermediate Steps In Erythroid, Megakaryocytic and Myeloid Lineage Specification Blood. 116: 4778-4778. DOI: 10.1182/Blood.V116.21.4778.4778 |
0.316 |
|
| 2009 |
Canaan A, Haviv I, Urban AE, Schulz VP, Hartman S, Zhang Z, Palejev D, Deisseroth AB, Lacy J, Snyder M, Gerstein M, Weissman SM. EBNA1 regulates cellular gene expression by binding cellular promoters. Proceedings of the National Academy of Sciences of the United States of America. 106: 22421-6. PMID 20080792 DOI: 10.1073/Pnas.0911676106 |
0.589 |
|
| 2009 |
Korbel JO, Tirosh-Wagner T, Urban AE, Chen XN, Kasowski M, Dai L, Grubert F, Erdman C, Gao MC, Lange K, Sobel EM, Barlow GM, Aylsworth AS, Carpenter NJ, Clark RD, ... ... Weissman S, et al. The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies. Proceedings of the National Academy of Sciences of the United States of America. 106: 12031-6. PMID 19597142 DOI: 10.1073/Pnas.0813248106 |
0.754 |
|
| 2009 |
Snyder M, Weissman S, Gerstein M. Personal phenotypes to go with personal genomes. Molecular Systems Biology. 5: 273. PMID 19455137 DOI: 10.1038/Msb.2009.32 |
0.38 |
|
| 2009 |
Canaan A, Schulz V, Mahajan M, Urban A, Weissman S. EBNA1—A virally encoded protein binds cellular host promoters in a unique sequence and directly interferes with cellular gene expression. Implications for genomics approaches in drug design Antiviral Research. 82: A69-A70. DOI: 10.1016/J.Antiviral.2009.02.171 |
0.626 |
|
| 2008 |
Kim PM, Lam HY, Urban AE, Korbel JO, Affourtit J, Grubert F, Chen X, Weissman S, Snyder M, Gerstein MB. Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history. Genome Research. 18: 1865-74. PMID 18842824 DOI: 10.1101/Gr.081422.108 |
0.64 |
|
| 2008 |
Pan X, Urban AE, Palejev D, Schulz V, Grubert F, Hu Y, Snyder M, Weissman SM. A procedure for highly specific, sensitive, and unbiased whole-genome amplification. Proceedings of the National Academy of Sciences of the United States of America. 105: 15499-504. PMID 18832167 DOI: 10.1073/Pnas.0808028105 |
0.568 |
|
| 2008 |
Pelizzola M, Koga Y, Urban AE, Krauthammer M, Weissman S, Halaban R, Molinaro AM. MEDME: an experimental and analytical methodology for the estimation of DNA methylation levels based on microarray derived MeDIP-enrichment. Genome Research. 18: 1652-9. PMID 18765822 DOI: 10.1101/Gr.080721.108 |
0.583 |
|
| 2008 |
Reed BD, Charos AE, Szekely AM, Weissman SM, Snyder M. Genome-wide occupancy of SREBP1 and its partners NFY and SP1 reveals novel functional roles and combinatorial regulation of distinct classes of genes. Plos Genetics. 4: e1000133. PMID 18654640 DOI: 10.1371/Journal.Pgen.1000133 |
0.586 |
|
| 2008 |
Korbel JO, Kim PM, Chen X, Urban AE, Weissman S, Snyder M, Gerstein MB. The current excitement about copy-number variation: how it relates to gene duplications and protein families. Current Opinion in Structural Biology. 18: 366-74. PMID 18511261 DOI: 10.1016/J.Sbi.2008.02.005 |
0.6 |
|
| 2008 |
Johnson DS, Li W, Gordon DB, Bhattacharjee A, Curry B, Ghosh J, Brizuela L, Carroll JS, Brown M, Flicek P, Koch CM, Dunham I, Bieda M, Xu X, Farnham PJ, ... ... Weissman S, et al. Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. Genome Research. 18: 393-403. PMID 18258921 DOI: 10.1101/Gr.7080508 |
0.358 |
|
| 2008 |
Wu JQ, Du J, Rozowsky J, Zhang Z, Urban AE, Euskirchen G, Weissman S, Gerstein M, Snyder M. Systematic analysis of transcribed loci in ENCODE regions using RACE sequencing reveals extensive transcription in the human genome. Genome Biology. 9: R3. PMID 18173853 DOI: 10.1186/Gb-2008-9-1-R3 |
0.66 |
|
| 2007 |
Korbel JO, Urban AE, Affourtit JP, Godwin B, Grubert F, Simons JF, Kim PM, Palejev D, Carriero NJ, Du L, Taillon BE, Chen Z, Tanzer A, Saunders AC, Chi J, ... ... Weissman SM, et al. Paired-end mapping reveals extensive structural variation in the human genome. Science (New York, N.Y.). 318: 420-6. PMID 17901297 DOI: 10.1126/Science.1149504 |
0.613 |
|
| 2007 |
Birney E, Stamatoyannopoulos JA, Dutta A, Guigó R, Gingeras TR, Margulies EH, Weng Z, Snyder M, Dermitzakis ET, Thurman RE, Kuehn MS, Taylor CM, Neph S, Koch CM, ... ... Weissman S, et al. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 447: 799-816. PMID 17571346 DOI: 10.1038/Nature05874 |
0.757 |
|
| 2007 |
Euskirchen GM, Rozowsky JS, Wei CL, Lee WH, Zhang ZD, Hartman S, Emanuelsson O, Stolc V, Weissman S, Gerstein MB, Ruan Y, Snyder M. Mapping of transcription factor binding regions in mammalian cells by ChIP: comparison of array- and sequencing-based technologies. Genome Research. 17: 898-909. PMID 17568005 DOI: 10.1101/Gr.5583007 |
0.364 |
|
| 2007 |
Zhang ZD, Paccanaro A, Fu Y, Weissman S, Weng Z, Chang J, Snyder M, Gerstein MB. Statistical analysis of the genomic distribution and correlation of regulatory elements in the ENCODE regions. Genome Research. 17: 787-97. PMID 17567997 DOI: 10.1101/Gr.5573107 |
0.396 |
|
| 2007 |
Rozowsky JS, Newburger D, Sayward F, Wu J, Jordan G, Korbel JO, Nagalakshmi U, Yang J, Zheng D, Guigó R, Gingeras TR, Weissman S, Miller P, Snyder M, Gerstein MB. The DART classification of unannotated transcription within the ENCODE regions: associating transcription with known and novel loci. Genome Research. 17: 732-45. PMID 17567993 DOI: 10.1101/Gr.5696007 |
0.421 |
|
| 2007 |
Gerstein MB, Bruce C, Rozowsky JS, Zheng D, Du J, Korbel JO, Emanuelsson O, Zhang ZD, Weissman S, Snyder M. What is a gene, post-ENCODE? History and updated definition. Genome Research. 17: 669-81. PMID 17567988 DOI: 10.1101/Gr.6339607 |
0.41 |
|
| 2007 |
Korbel JO, Urban AE, Grubert F, Du J, Royce TE, Starr P, Zhong G, Emanuel BS, Weissman SM, Snyder M, Gerstein MB. Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome. Proceedings of the National Academy of Sciences of the United States of America. 104: 10110-5. PMID 17551006 DOI: 10.1073/Pnas.0703834104 |
0.602 |
|
| 2007 |
Emanuelsson O, Nagalakshmi U, Zheng D, Rozowsky JS, Urban AE, Du J, Lian Z, Stolc V, Weissman S, Snyder M, Gerstein MB. Assessing the performance of different high-density tiling microarray strategies for mapping transcribed regions of the human genome. Genome Research. 17: 886-97. PMID 17119069 DOI: 10.1101/Gr.5014606 |
0.643 |
|
| 2006 |
Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M. High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. Proceedings of the National Academy of Sciences of the United States of America. 103: 4534-9. PMID 16537408 DOI: 10.1073/Pnas.0511340103 |
0.591 |
|
| 2006 |
Lian J, Lian Z, Karpikov A, Mahajan M, Gerstein M, Snyde M, Weissman S. Genomic Distribution of Transcripts and DNA Associated Proteins in One Percent of the Genome of Erythroid and Myeloid Cells. Blood. 108: 4201-4201. DOI: 10.1182/Blood.V108.11.4201.4201 |
0.46 |
|
| 2005 |
Hartman SE, Bertone P, Nath AK, Royce TE, Gerstein M, Weissman S, Snyder M. Global changes in STAT target selection and transcription regulation upon interferon treatments. Genes & Development. 19: 2953-68. PMID 16319195 DOI: 10.1101/Gad.1371305 |
0.358 |
|
| 2005 |
Royce TE, Rozowsky JS, Bertone P, Samanta M, Stolc V, Weissman S, Snyder M, Gerstein M. Issues in the analysis of oligonucleotide tiling microarrays for transcript mapping. Trends in Genetics : Tig. 21: 466-75. PMID 15979196 DOI: 10.1016/J.Tig.2005.06.007 |
0.403 |
|
| 2004 |
White EJ, Emanuelsson O, Scalzo D, Royce T, Kosak S, Oakeley EJ, Weissman S, Gerstein M, Groudine M, Snyder M, Schübeler D. DNA replication-timing analysis of human chromosome 22 at high resolution and different developmental states. Proceedings of the National Academy of Sciences of the United States of America. 101: 17771-6. PMID 15591350 DOI: 10.1073/Pnas.0408170101 |
0.443 |
|
| 2004 |
Bertone P, Stolc V, Royce TE, Rozowsky JS, Urban AE, Zhu X, Rinn JL, Tongprasit W, Samanta M, Weissman S, Gerstein M, Snyder M. Global identification of human transcribed sequences with genome tiling arrays. Science (New York, N.Y.). 306: 2242-6. PMID 15539566 DOI: 10.1126/Science.1103388 |
0.667 |
|
| 2004 |
Brazma A, Freeman T, Gardiner K, Weissman S, Werner T, Korn B. Report on the thirteenth international workshop on the identification and functional, evolutionary and expression analysis of transcribed sequences: comparative and functional genomics workshop. Cytogenetic and Genome Research. 105: 11-7. PMID 15218252 DOI: 10.1159/000078003 |
0.387 |
|
| 2004 |
Euskirchen G, Royce TE, Bertone P, Martone R, Rinn JL, Nelson FK, Sayward F, Luscombe NM, Miller P, Gerstein M, Weissman S, Snyder M. CREB binds to multiple loci on human chromosome 22. Molecular and Cellular Biology. 24: 3804-14. PMID 15082775 DOI: 10.1128/Mcb.24.9.3804-3814.2004 |
0.434 |
|
| 2003 |
Lian Z, Euskirchen G, Rinn J, Martone R, Bertone P, Hartman S, Royce T, Nelson K, Sayward F, Luscombe N, Yang J, Li JL, Miller P, Urban AE, Gerstein M, ... Weissman S, et al. Identification of novel functional elements in the human genome. Cold Spring Harbor Symposia On Quantitative Biology. 68: 317-22. PMID 15338632 DOI: 10.1101/Sqb.2003.68.317 |
0.579 |
|
| 2003 |
Martone R, Euskirchen G, Bertone P, Hartman S, Royce TE, Luscombe NM, Rinn JL, Nelson FK, Miller P, Gerstein M, Weissman S, Snyder M. Distribution of NF-kappaB-binding sites across human chromosome 22. Proceedings of the National Academy of Sciences of the United States of America. 100: 12247-52. PMID 14527995 DOI: 10.1073/Pnas.2135255100 |
0.376 |
|
| 2003 |
Rinn JL, Euskirchen G, Bertone P, Martone R, Luscombe NM, Hartman S, Harrison PM, Nelson FK, Miller P, Gerstein M, Weissman S, Snyder M. The transcriptional activity of human Chromosome 22. Genes & Development. 17: 529-40. PMID 12600945 DOI: 10.1101/Gad.1055203 |
0.459 |
|
| 2002 |
Werner T, Weissman S, Hedges SB, Gardiner K. Report on the twelfth international workshop on the identification of transcribed sequences: functional, expression and evolutionary analysis. Cytogenetic and Genome Research. 98: 109-17. PMID 12697992 DOI: 10.1159/000069801 |
0.341 |
|
| 2000 |
Yang YH, Chen YH, Zhang CY, Nimmakayalu MA, Ward DC, Weissman S. Cloning and characterization of two mouse genes with homology to the yeast Sir2 gene. Genomics. 69: 355-69. PMID 11056054 DOI: 10.1006/Geno.2000.6360 |
0.386 |
|
| 1998 |
Hisama FM, Oshima J, Yu CE, Fu YH, Mulligan J, Weissman SM, Schellenberg GD. Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region. Genomics. 52: 352-7. PMID 9790753 DOI: 10.1006/Geno.1998.5475 |
0.342 |
|
| 1996 |
Gruen JR, Nalabolu SR, Chu TW, Bowlus C, Fan WF, Goei VL, Wei H, Sivakamasundari R, Liu Y, Xu HX, Parimoo S, Nallur G, Ajioka R, Shukla H, Bray-Ward P, ... ... Weissman SM, et al. A transcription map of the major histocompatibility complex (MHC) class I region. Genomics. 36: 70-85. PMID 8812418 DOI: 10.1006/Geno.1996.0427 |
0.304 |
|
| 1995 |
Lamerdin JE, Athwal RS, Kansara MS, Sandhu AK, Patanjali SR, Weissman SM, Carrano AV. Chromosomal localization and expressed sequence tag generation of clones from a normalized human adult thymus cDNA library. Genome Research. 5: 359-67. PMID 8750195 DOI: 10.1101/gr.5.4.359 |
0.306 |
|
| 1995 |
Min J, Shukla H, Kozono H, Bronson SK, Weissman SM, Chaplin DD. A novel Creb family gene telomeric of HLA-DRA in the HLA complex. Genomics. 30: 149-56. PMID 8586413 DOI: 10.1006/Geno.1995.9891 |
0.31 |
|
| 1995 |
Tassone F, Xu H, Burkin H, Weissman S, Gardiner K. cDNA selection from 10 Mb of chromosome 21 DNA: efficiency in transcriptional mapping and reflections of genome organization. Human Molecular Genetics. 4: 1509-18. PMID 8541833 DOI: 10.1093/Hmg/4.9.1509 |
0.431 |
|
| 1995 |
Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, Ashkenazi M, Pecker I, Frydman M, Harnik R, Patanjali SR, ... ... Weissman SM, et al. A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science (New York, N.Y.). 268: 1749-53. PMID 7792600 |
0.437 |
|
| 1993 |
Das Gupta R, Morrow B, Marondel I, Parimoo S, Goei VL, Gruen J, Weissman S, Skoultchi A, Kucherlapati R. An integrated approach for identifying and mapping human genes. Proceedings of the National Academy of Sciences of the United States of America. 90: 4364-8. PMID 8506274 DOI: 10.1073/Pnas.90.10.4364 |
0.33 |
|
| 1993 |
Aso T, Tsai P, Kawaguchi T, Menninger JC, Kitajima S, Yasukochi Y, Ward DC, Weissman SM. Assignment of the human GTF2F1 gene to chromosome 19p13.3. Genomics. 16: 252-3. PMID 8486367 DOI: 10.1006/Geno.1993.1168 |
0.308 |
|
| 1993 |
Fan WF, Wei X, Shukla H, Parimoo S, Xu H, Sankhavaram P, Li Z, Weissman SM. Application of cDNA selection techniques to regions of the human MHC. Genomics. 17: 575-81. PMID 8244372 |
0.316 |
|
| 1991 |
Pati UK, Weissman SM. Isolation and molecular characterization of a cDNA encoding the 23-kDa subunit of human RNA polymerase II. The Journal of Biological Chemistry. 266: 13468. PMID 2071613 |
0.585 |
|
| 1991 |
Swaroop A, Xu JZ, Agarwal N, Weissman SM. A simple and efficient cDNA library subtraction procedure: isolation of human retina-specific cDNA clones. Nucleic Acids Research. 19: 1954. PMID 2030979 DOI: 10.1093/Nar/19.8.1954 |
0.418 |
|
| 1991 |
Swaroop A, Agarwal N, Gruen JR, Bick D, Weissman SM. Differential expression of novel Gs alpha signal transduction protein cDNA species. Nucleic Acids Research. 19: 4725-9. PMID 1716359 DOI: 10.1093/Nar/19.17.4725 |
0.413 |
|
| 1990 |
Vasavada HA, Ganguly S, Chorney M, Mathur R, Shukla H, Swaroop A, Weissman SM. pSH4: a mammalian cDNA expression vector. Nucleic Acids Research. 18: 3668. PMID 2362830 DOI: 10.1093/Nar/18.12.3668 |
0.372 |
|
| 1990 |
Shukla H, Swaroop A, Srivastava R, Weissman SM. The mRNA of a human class I gene HLA G/HLA 6.0 exhibits a restricted pattern of expression. Nucleic Acids Research. 18: 2189. PMID 2336406 DOI: 10.1093/Nar/18.8.2189 |
0.414 |
|
| 1990 |
Kandpal RP, Ward DC, Weissman SM. Selective enrichment of a large size genomic DNA fragment by affinity capture: an approach for genome mapping. Nucleic Acids Research. 18: 1789-95. PMID 2336356 DOI: 10.1093/Nar/18.7.1789 |
0.32 |
|
| 1990 |
Tanaka M, Nolan JA, Bhargava AK, Rood K, Collins FS, Weissman SM, Forget BG, Chamberlain JW. Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin. Annals of the New York Academy of Sciences. 612: 167-78. PMID 2291546 DOI: 10.1111/J.1749-6632.1990.Tb24303.X |
0.416 |
|
| 1990 |
Pati UK, Weissman SM. The amino acid sequence of the human RNA polymerase II 33-kDa subunit hRPB 33 is highly conserved among eukaryotes. The Journal of Biological Chemistry. 265: 8400-3. PMID 2187864 |
0.6 |
|
| 1989 |
Pati UK, Weissman SM. Isolation and molecular characterization of a cDNA encoding the 23-kDa subunit of human RNA polymerase II. The Journal of Biological Chemistry. 264: 13114-21. PMID 2753903 |
0.597 |
|
| 1988 |
Swaroop A, Weissman SM. Charon BS (+) and (-), versatile λ phage vectors for constructing directional cDNA libraries and their efficient transfer to plasmids Nucleic Acids Research. 16: 8739. PMID 2971160 DOI: 10.1093/Nar/16.17.8739 |
0.354 |
|
| 1987 |
Smith CL, Lawrance SK, Gillespie GA, Cantor CR, Weissman SM, Collins FS. Strategies for mapping and cloning macroregions of mammalian genomes Methods in Enzymology. 151: 461-489. PMID 2828836 DOI: 10.1016/S0076-6879(87)51038-2 |
0.451 |
|
| 1987 |
Srivastava R, Chorney MJ, Lawrance SK, Pan J, Smith Z, Smith CL, Weissman SM. Structure, expression, and molecular mapping of a divergent member of the class I HLA gene family Proceedings of the National Academy of Sciences of the United States of America. 84: 4224-4228. PMID 2438694 DOI: 10.1073/pnas.84.12.4224 |
0.302 |
|
| 1986 |
Metherall JE, Collins FS, Pan J, Weissman SM, Forget BG. Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron Embo Journal. 5: 2551-2557. PMID 3780671 DOI: 10.1002/J.1460-2075.1986.Tb04534.X |
0.366 |
|
| 1986 |
Lawrence SK, Srivastava R, Rigas B, Chorney MJ, Gillespie GA, Smith CL, Cantor CR, Collins FS, Weissman SM. Molecular approaches to the characterization of megabase regions of DNA: Applications to the human major histocompatibility complex Cold Spring Harbor Symposia On Quantitative Biology. 51: 123-130. PMID 3472708 DOI: 10.1101/Sqb.1986.051.01.015 |
0.4 |
|
| 1985 |
Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin Nature. 313: 325-326. PMID 2578620 DOI: 10.1038/313325A0 |
0.425 |
|
| 1985 |
Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin Progress in Clinical and Biological Research. 191: 107-124. PMID 2413468 |
0.332 |
|
| 1985 |
Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia. Annals of the New York Academy of Sciences. 445: 159-69. PMID 2409868 DOI: 10.1111/J.1749-6632.1985.Tb17185.X |
0.336 |
|
| 1984 |
Collins FS, Weissman SM. The molecular genetics of human hemoglobin Progress in Nucleic Acid Research and Molecular Biology. 31: 315-462. PMID 6397774 |
0.363 |
|
| 1984 |
Stoeckert CJ, Collins FS, Weissman SM. Human fetal globin DNA sequences suggest novel conversion event Nucleic Acids Research. 12: 4469-4479. PMID 6330670 DOI: 10.1093/nar/12.11.4469 |
0.46 |
|
| 1984 |
Collins FS, Boehm CD, Waber PG, Stoeckert CJ, Weissman SM, Forget BG, Kazazian HH. Concordance of a point mutation 5' to the (G)γ globin gene with (G)γβ+ hereditary persistence of fetal hemoglobin in the black population Blood. 64: 1292-1296. PMID 6208955 |
0.378 |
|
| 1984 |
Collins FS, Stoeckert CJ, Serjeant GR, Forget BG, Weissman SM. (G)γβ+ Hereditary persistence of fetal hemoglobin: Cosmid cloning and identification of a specific mutation 5' to the (G)γ gene Proceedings of the National Academy of Sciences of the United States of America. 81: 4894-4898. PMID 6205403 DOI: 10.1073/Pnas.81.15.4894 |
0.433 |
|
| 1984 |
Collins FS, Weissman SM. Directional cloning of DNA fragments at a large distance from an initial probe: A circularization method Proceedings of the National Academy of Sciences of the United States of America. 81: 6812-6816. PMID 6093122 DOI: 10.1073/Pnas.81.21.6812 |
0.425 |
|
| 1984 |
Collins F, Boehm C, Waber P, Stoeckert CJ, Weissman S, Forget B, Kazazian HJ. Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population Blood. 64: 1292-1296. DOI: 10.1182/Blood.V64.6.1292.1292 |
0.375 |
|
| 1983 |
Fukumaki Y, Collins F, Kole R, Stoeckert C, Jagadeeswaran P, Duncan C, Weissman S. Sequences of Human Repetitive DNA, Non- -globin Genes, and Major Histocompatibility Locus Genes: I. Repeated-sequence DNA Cold Spring Harbor Symposia On Quantitative Biology. 47: 1079-1086. DOI: 10.1101/Sqb.1983.047.01.120 |
0.464 |
|
| 1982 |
Jagadeeswaran P, Biro PA, Tuan D, Pan J, Forget BG, Weissman SM. Interspersed repetitive DNA sequences of the human genome: are they transposons? Progress in Clinical and Biological Research. 103: 29-35. PMID 6298805 |
0.309 |
|
| 1982 |
Jagadeeswaran P, Tuan D, Forget BG, Weissman SM. A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin Nature. 296: 469-470. PMID 6174873 DOI: 10.1038/296469A0 |
0.305 |
|
| 1981 |
Pan J, Elder JT, Duncan CH, Weissman SM. Structural analysis of interspersed repetitive polymerase III transcription units in human DNA Nucleic Acids Research. 9: 1151-1170. PMID 7232213 |
0.303 |
|
| 1980 |
Spritz RA, DeRiel JK, Forget BG, Weissman SM. Complete nucleotide sequence of the human δ-globin gene Cell. 21: 639-646. PMID 7438204 DOI: 10.1016/0092-8674(80)90427-4 |
0.301 |
|
| 1978 |
Reddy VB, Thimmappaya B, Dhar R, Subramanian KN, Zain BS, Pan J, Ghosh PK, Celma ML, Weissman SM. The genome of simian virus 40. Science (New York, N.Y.). 200: 494-502. PMID 205947 DOI: 10.1126/SCIENCE.205947 |
0.389 |
|
| Show low-probability matches. |