HistCite - The sequence of the human genome (Venter)

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#	Date / Author / Journal	LCS	GCS	LCR	CR
2401	3327 Dalla E, Mignone F, Verardo R, Marchionni L, Marzinotto S, et al. Discovery of 342 putative new genes from the analysis of 5 '-end-sequenced full-length-enriched cDNA human transcripts GENOMICS. 2005 JUN; 85 (6): 739-751	0	4	7	30
2402	3400 Ge XJ, Yamamoto S, Tsutsumi S, Midorikawa Y, Ihara S, et al. Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues GENOMICS. 2005 AUG; 86 (2): 127-141	1	57	6	42
2403	3465 Hancock DK, Tully LA, Levin BC A Standard Reference Material to determine the sensitivity of techniques for detecting low-frequency mutations, SNPs, and heteroplasmies in mitochondrial DNA GENOMICS. 2005 OCT; 86 (4): 446-461	0	10	2	38
2404	3533 Puente XS, Gutierrez-Fernandez A, Ordonez GR, Hillier LDW, Lopez-Otin C Comparative genomic analysis of human and chimpanzee proteases GENOMICS. 2005 DEC; 86 (6): 638-647	0	18	5	59
2405	3534 Meyers SN, Rogatcheva MB, Larkin DM, Yerle M, Milan D, et al. Piggy-BACing the human genome - II. A high-resolution, physically anchored, comparative map of the porcine autosomes GENOMICS. 2005 DEC; 86 (6): 739-+	4	57	4	38
2406	3657 Li JG, Liljedahl U, Heng CK Tag/anti-tag liquid-phase primer extension array: A flexible and versatile genotyping platform GENOMICS. 2006 JAN; 87 (1): 151-157	0	1	1	31
2407	3774 Brzoska PM, Brown C, Cassel M, Ceccardi T, Di Francisco V, et al. An efficient and high-throughput approach for experimental validation of novel human gene predictions GENOMICS. 2006 APR; 87 (4): 437-445	1	4	10	46
2408	3803 Feltus FA, Lee EK, Costello JF, Plass C, Vertino PM DNA motifs associated with aberrant CpG island methylation GENOMICS. 2006 MAY; 87 (5): 572-579	2	23	3	43
2409	3941 Bjarnadottir TK, Gloriam DE, Hellstrand SH, Kristiansson H, Fredriksson R, et al. Comprehensive repertoire and phylogenetic analysis of the G protein-coupled receptors in human and mouse GENOMICS. 2006 SEP; 88 (3): 263-273	2	29	10	40
2410	4012 Haitina T, Lindblom J, Renstrom T, Fredriksson R Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system GENOMICS. 2006 DEC; 88 (6): 779-790	1	16	5	45
#	Date / Author / Journal	LCS	GCS	LCR	CR
2411	4113 Vanhoutteghem A, Djian P The human basonuclin 2 gene has the potential to generate nearly 90,000 mRNA isoforms encoding over 2000 different proteins GENOMICS. 2007 JAN; 89 (1): 44-58	0	4	5	30
2412	4177 Lamesch P, Li N, Milstein S, Fan CY, Hao T, et al. h0RFeome v3.1: A resource of human open reading frames representing over 10,000 human genes GENOMICS. 2007 MAR; 89 (3): 307-315	0	33	11	39
2413	4284 Torkamani A, Schork NJ Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family GENOMICS. 2007 JUL; 90 (1): 49-58	1	9	5	42
2414	4328 Langille MGI, Clark DV Parent genes of retrotransposition-generated gene duplicates in Drosophila melanogaster have distinct expression profiles GENOMICS. 2007 SEP; 90 (3): 334-343	1	4	2	44
2415	4542 Tan K, Tegner J, Ravasi T Integrated approaches to uncovering transcription regulatory networks in mammalian cells GENOMICS. 2008 MAR; 91 (3): 219-231	0	5	9	132
2416	4543 Ji XL, Zhao SY DA and Xiao-two giant and composite LTR-retrotransposon-like elements identified in the human genome GENOMICS. 2008 MAR; 91 (3): 249-258	1	2	8	39
2417	4652 Louro R, El-Jundi T, Nakaya HI, Reis EM, Verjovski-Almeida S Conserved tissue expression signatures of intronic noncoding RNAs transcribed from human and mouse loci GENOMICS. 2008 JUL; 92 (1): 18-25	0	3	12	46
2418	4676 Zhang DF, Yang QY, Ding Y, Cao XF, Xue YB, et al. Cytological characterization of the tandem repetitive sequences and their methylation status in the Antirrhinum majus genome GENOMICS. 2008 AUG; 92 (2): 107-114	0	0	3	38
2419	4701 Lee TM, Lipovich L Structural differences of orthologous genes: Insights from human-primate comparisons GENOMICS. 2008 SEP; 92 (3): 134-143	0	0	6	51
2420	4761 Morozova O, Marra MA Applications of next-generation sequencing technologies in functional genomics GENOMICS. 2008 NOV; 92 (5): 255-264	2	35	6	111
#	Date / Author / Journal	LCS	GCS	LCR	CR
2421	4893 Pettersson E, Lundeberg J, Ahmadian A Generations of sequencing technologies GENOMICS. 2009 FEB; 93 (2): 105-111	1	12	6	40
2422	4967 Wilkening S, Chen BW, Bermejo JL, Canzian F Is there still a need for candidate gene approaches in the era of genome-wide association studies? GENOMICS. 2009 MAY; 93 (5): 415-419	0	1	4	20
2423	894 Hoffmann W, Latza U, Ahrens W, Greiser KH, Kroke A, et al. Biological markers in epidemiology: Concepts, applications, perspectives (Part II) GESUNDHEITSWESEN. 2002 MAR; 64 (3): 145-152	0	0	2	65
2424	1944 Wilson VA, Gallagher JT, Merry CLR Heparan sulfate 2-O-sulfotransferase (Hs2st) and mouse development GLYCOCONJUGATE JOURNAL. 2003 MAY-JUN; 19 (4-5): 347-354	0	17	2	58
2425	4066 Wigglesworth MJ, Wolfe LA, Wise A Orphan seven transmembrane receptor screening GPCRS: FROM DEORPHANIZATION TO LEAD STRUCTURE IDENTIFICATION. 2007; 2: 105-143	0	0	8	195
2426	3103 Breimer E, Goldberg M, Hollinger D, Lim D Discovering optimization algorithms through automated learning GRAPHS AND DISCOVERY. 2005; 69: 7-25	0	1	1	49
2427	3104 Trejo JL, Carro E, Burks DJ Experimental models for understanding the role of insulin-like growth factor-I and its receptor during development GROWTH HORMONE/INSULIN-LIKE GROWTH FACTOR AXIS DURING DEVELOPMENT. 2005; 567: 27-53	0	2	2	116
2428	4404 Park NH, Song H, Chung YH Molecular Pathogenesis of Hepatitis-B-virus-associated Hepatocellular Carcinoma GUT AND LIVER. 2007 DEC; 1 (2): 101-117	0	0	3	132
2429	3105 te Velde ER Is women's emancipation still compatible with reproduction in this century? GYNAECOLOGY, OBSTETRICS, AND REPRODUCTIVE MEDICINE IN DAILY PRACTICE. 2005; 1279: 58-67	0	0	1	30
2430	3606 Guo SW Association of endometriosis risk and genetic polymorphisms involving sex steroid biosynthesis and their receptors: A meta-analysis GYNECOLOGIC AND OBSTETRIC INVESTIGATION. 2006; 61 (2): 90-105	0	13	2	57
#	Date / Author / Journal	LCS	GCS	LCR	CR
2431	1701 Gray JW, Suzuki S, Kuo WL, Polikoff D, Deavers M, et al. Specific keynote: Genome copy number abnormalities in ovarian cancer GYNECOLOGIC ONCOLOGY. 2003 JAN; 88 (1): S16-S21	0	22	2	70
2432	2553 Ferguson SE, Olshen AB, Viale A, Awtrey CS, Barakat RR, et al. Gene expression profiling of tamoxifen-associated uterine cancers: evidence for two molecular classes of endometrial carcinoma GYNECOLOGIC ONCOLOGY. 2004 FEB; 92 (2): 719-725	2	18	1	19
2433	4178 Walsh CS, Miller CW, Karlan BY, Koeffler HP Association between a functional single nucleotide polyrnorphism in the MDM2 gene and sporadic endometrial cancer risk GYNECOLOGIC ONCOLOGY. 2007 MAR; 104 (3): 660-664	1	22	2	39
2434	3194 Corral J, Vicente V, Carrell RW Thrombosis as a conformational disease HAEMATOLOGICA. 2005 FEB; 90 (2): 238-246	0	10	1	37
2435	3365 Berntorp E, Astermark J, Donfield SM, Nelson GW, Oldenburg J, et al. Haemophilia Inhibitor Genetics Study - evaluation of a model for studies of complex diseases using linkage and association methods HAEMOPHILIA. 2005 JUL; 11 (4): 427-429	0	5	4	23
2436	4013 [Anon] Guiding regulatory reform in reproduction and genetics HARVARD LAW REVIEW. 2006 DEC; 120 (2): 574-596	0	0	1	58
2437	186 Sklar P The genomic approach to candidate genes HARVARD REVIEW OF PSYCHIATRY. 2001 JUL-AUG; 9 (4): 197-207	0	0	2	64
2438	3727 Scolnick EM, Petryshen T, Sklar P Schizophrenia: Do the genetics and neurobiology of neuregulin provide a pathogenesis model? HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 64-77	0	2	6	74
2439	3728 Roffman JL, Weiss AP, Goff DC, Rauch SL, Weinberger DR Neuroimaging-genetic paradigms: A new approach to investigate the pathophysiology and treatment of cognitive deficits in schizophrenia HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 78-91	0	20	3	126
2440	2077 Amundson SA, Fornace AJ Monitoring human radiation exposure by gene expression profiling: Possibilities and pitfalls HEALTH PHYSICS. 2003 JUL; 85 (1): 36-42	0	18	2	36
#	Date / Author / Journal	LCS	GCS	LCR	CR
2441	2132 Resnik DB Are DNA patents bad for medicine? HEALTH POLICY. 2003 AUG; 65 (2): 181-197	0	3	1	54
2442	1508 Shackel NA, Gorrell MD, McCaughan GW Gene array analysis and the liver HEPATOLOGY. 2002 DEC; 36 (6): 1313-1325	2	30	2	121
2443	1879 Thorgeirsson SS Hunting for tumor suppressor genes in liver cancer HEPATOLOGY. 2003 APR; 37 (4): 739-741	0	8	4	23
2444	2183 Shackel NA, McGuinness PH, Abbott CA, Gorrell MD, McCaughan GW Novel differential gene expression in human cirrhosis detected by suppression subtractive hybridization HEPATOLOGY. 2003 SEP; 38 (3): 577-588	1	25	2	50
2445	2646 Zhang DY, Sabla G, Shivakumar P, Tiao G, Sokol RJ, et al. Coordinate expression of regulatory genes differentiates embryonic and perinatal forms of biliary atresia HEPATOLOGY. 2004 APR; 39 (4): 954-962	0	22	1	34
2446	4014 Juran BD, Lazaridis KN Genomics and complex liver disease: Challenges and opportunities HEPATOLOGY. 2006 DEC; 44 (6): 1380-1390	1	11	9	84
2447	1945 Sverdlov ED DNA in a cell: From a molecular icon to the problem of "what is life?" HERALD OF THE RUSSIAN ACADEMY OF SCIENCES. 2003 MAY-JUN; 73 (3): 262-269	0	2	9	29
2448	4285 Portin P Evolution of man in the light of molecular genetics: a review. Part I. Our evolutionary history and genomics HEREDITAS. 2007 JUL; 144 (3): 80-95	0	1	12	130
2449	5045 Sato K, Nankaku N, Takeda K A high-density transcript linkage map of barley derived from a single population HEREDITY. 2009 AUG; 103 (2): 110-117	0	1	1	55
2450	34 Prestegard JH High resolution NMR of biomolecules HIGH MAGNETIC FIELDS. 2001; 595: 426-434	0	2	3	21
#	Date / Author / Journal	LCS	GCS	LCR	CR
2451	671 Alur R, Belta C, Ivancic N, Kumar V, Rubin H, et al. Visual programming for modeling and simulation of biomolecular regulatory networks HIGH PERFORMANCE COMPUTING - HIPC 2002, PROCEEDINGS. 2002; 2552: 702-712	0	0	1	17
2452	1260 Roix J, Misteli T Genomes, proteomes, and dynamic networks in the cell nucleus HISTOCHEMISTRY AND CELL BIOLOGY. 2002 AUG; 118 (2): 105-116	0	23	3	79
2453	965 Finta C, Warner SC, Zaphiropoulos PG Intergenic mRNAs. Minor gene products or tools of diversity? HISTOLOGY AND HISTOPATHOLOGY. 2002 APR; 17 (2): 677-682	0	9	5	46
2454	2184 Haas DW, Wilkinson GR, Kuritzkes DR, Richman DD, Nicotera J, et al. A multi-investigator/institutional DNA bank for AIDS-related human genetic studies: AACTG Protocol A5128 HIV CLINICAL TRIALS. 2003 SEP-OCT; 4 (5): 287-300	4	24	2	40
2455	5026 Basham RJ, Richardson DM, Sutcliffe CB, Haas DW Effect of HIV-1 Infection on Human DNA Yield from Saliva HIV CLINICAL TRIALS. 2009 JUL-AUG; 10 (4): 282-285	0	0	4	19
2456	35 Bouillon R The future of endocrinology and the endocrinologist of the future HORMONE RESEARCH. 2001; 56: 98-105	0	1	1	3
2457	1630 Polychronakos C Impact of the human genome project on pediatric endocrinology HORMONE RESEARCH. 2003; 59 (2): 55-65	1	3	6	44
2458	672 Pucci-Minafra I, Fontana S, Cancemi P, Alaimo G, Minafra S Proteomic patterns of cultured breast cancer cells and epithelial mammary cells HORMONE-RELATED TUMORS: NOVEL APPROACHES TO PREVENTION AND TREATMENT. 2002; 963: 122-139	3	24	2	18
2459	4443 Ribeiro EO, Walter MEMT, Costa MM, Togawa R, Pappas G p2pBIOFOCO: Proposing a Peer-to-Peer System for Distributed BLAST Execution HPCC 2008: 10TH IEEE INTERNATIONAL CONFERENCE ON HIGH PERFORMANCE COMPUTING AND COMMUNICATIONS, PROCEEDINGS. 2008; : 594-601	0	0	2	36
2460	2133 Eckhardt RB Polymorphisms past and present HUMAN BIOLOGY. 2003 AUG; 75 (4): 559-575	0	1	1	76
#	Date / Author / Journal	LCS	GCS	LCR	CR
2461	2277 Gottlieb G On making behavioral genetics truly developmental HUMAN DEVELOPMENT. 2003 NOV-DEC; 46 (6): 337-355	0	30	1	66
2462	230 Willett-Brozick JE, Savul SA, Richey LE, Baysal BE Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation HUMAN GENETICS. 2001 AUG; 109 (2): 216-223	1	21	2	47
2463	371 Spyrou G, Wilson W, Padilla CA, Holmgren A, Miranda-Vizuete A A genome-wide survey of human thioredoxin and glutaredoxin family pseudogenes HUMAN GENETICS. 2001 OCT; 109 (4): 429-439	2	7	3	51
2464	823 Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson JT, Syrjakoski K, et al. A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes HUMAN GENETICS. 2002 FEB; 110 (2): 111-121	0	28	2	30
2465	1509 Amsellem S, Briffaut D, Carrie A, Rabes JP, Girardet JP, et al. Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia HUMAN GENETICS. 2002 DEC; 111 (6): 501-510	2	30	2	53
2466	1702 Speckman RA, Daw JAW, Helms C, Duan SH, Cao L, et al. Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility HUMAN GENETICS. 2003 JAN; 112 (1): 34-41	0	37	1	46
2467	1946 Buzdin A, Ustyugova S, Gogvadze E, Lebedev Y, Hunsmann G, et al. Genome-wide targeted search for human specific and polymorphic L1 integrations HUMAN GENETICS. 2003 MAY; 112 (5-6): 527-533	4	18	3	27
2468	3882 Tang H, Jorgenson E, Gadde M, Kardia SLR, Rao DC, et al. Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans HUMAN GENETICS. 2006 JUL; 119 (6): 624-633	0	19	1	34
2469	4114 Zhang XZ, Mahmudi-Azer S, Connett JE, Anthonisen NR, He JQ, et al. Association of Hck genetic polymorphisms with gene expression and COPD HUMAN GENETICS. 2007 JAN; 120 (5): 681-690	1	4	3	34
2470	4894 Zhang W, Duan SW, Bleibel WK, Wisel SA, Huang RS, et al. Identification of common genetic variants that account for transcript isoform variation between human populations HUMAN GENETICS. 2009 FEB; 125 (1): 81-93	1	4	6	59
#	Date / Author / Journal	LCS	GCS	LCR	CR
2471	5169 Vorechovsky I Transposable elements in disease-associated cryptic exons HUMAN GENETICS. 2010 FEB; 127 (2): 135-154	0	0	6	158
2472	673 DeWan AT, Parrado AR, Matise TC, Leal SM Map error reduction: Using genetic and sequence-based physical maps to order closely linked markers HUMAN HEREDITY. 2002; 54 (1): 34-44	0	4	8	21
2473	2416 Halldorsson BV, Istrail S, De La Vega FM Optimal selection of SNP markers for disease association studies HUMAN HEREDITY. 2004; 58 (3-4): 190-202	3	32	7	58
2474	395 Goodstadt L, Ponting CR Sequence variation and disease in the wake of the draft human genome HUMAN MOLECULAR GENETICS. 2001 OCT 1; 10 (20): 2209-2214	4	19	3	24
2475	396 Horvath JE, Bailey JA, Locke DP, Eichler EE Lessons from the human genome: transitions between euchromatin and heterochromatin HUMAN MOLECULAR GENETICS. 2001 OCT 1; 10 (20): 2215-2223	8	64	2	90
2476	397 Miller MP, Kumar S Understanding human disease mutations through the use of interspecific genetic variation HUMAN MOLECULAR GENETICS. 2001 OCT 2; 10 (21): 2319-2328	3	115	2	39
2477	478 Takai D, Gonzales FA, Tsai YC, Thayer MJ, Jones PA Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer HUMAN MOLECULAR GENETICS. 2001 NOV 1; 10 (23): 2619-2626	1	72	1	28
2478	769 Watanabe Y, Fujiyama A, Ichiba Y, Hattori M, Yada T, et al. Chromosome-wide assessment of replication timing for human chromosomes 11q and 21q: disease-related genes in timing-switch regions HUMAN MOLECULAR GENETICS. 2002 JAN 1; 11 (1): 13-21	4	60	1	31
2479	993 Thaung C, West K, Clark BJ, McKie L, Morgan JE, et al. Novel ENU-induced eye mutations in the mouse: models for human eye disease HUMAN MOLECULAR GENETICS. 2002 APR 1; 11 (7): 755-767	1	50	4	63
2480	1276 Coleman SL, Buckland PR, Hoogendoorn B, Guy C, Smith K, et al. Experimental analysis of the annotation of promoters in the public database HUMAN MOLECULAR GENETICS. 2002 AUG 1; 11 (16): 1817-1821	2	20	3	14
#	Date / Author / Journal	LCS	GCS	LCR	CR
2481	1277 Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, et al. Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6 HUMAN MOLECULAR GENETICS. 2002 AUG 1; 11 (16): 1887-1898	1	33	2	50
2482	1352 Saarela J, Fejzo MS, Chen D, Finnila S, Parkkonen M, et al. Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24 HUMAN MOLECULAR GENETICS. 2002 SEP 15; 11 (19): 2257-2267	1	27	1	59
2483	1353 Wang PJ, Page DC Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis HUMAN MOLECULAR GENETICS. 2002 SEP 15; 11 (19): 2341-2346	4	36	2	32
2484	1396 Stamm S Signals and their transduction pathways regulating alternative splicing: a new dimension of the human genome HUMAN MOLECULAR GENETICS. 2002 OCT 1; 11 (20): 2409-2416	4	109	8	101
2485	1784 Duan JB, Wainwright MS, Comeron JM, Saitou N, Sanders AR, et al. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor HUMAN MOLECULAR GENETICS. 2003 FEB 1; 12 (3): 205-216	8	240	2	59
2486	1902 Emes RD, Goodstadt L, Winter EE, Ponting CP Comparison of the genomes of human and mouse lays the foundation of genome zoology HUMAN MOLECULAR GENETICS. 2003 APR 1; 12 (7): 701-709	9	59	6	119
2487	2034 Gong ML, Zhang HY, Schulz H, Lee YA, Sun K, et al. Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1273-1277	0	31	2	39
2488	2035 Semenova E, Wang XF, Jablonski MM, Levorse J, Tilghman SM An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1301-1312	0	21	6	51
2489	2036 Ejima Y, Yang LC Trans mobilization of genomic DNA as a mechanism for retrotransposon-mediated exon shuffling HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1321-1328	2	25	5	37
2490	2209 Hoogendoorn B, Coleman SL, Guy CA, Smith K, Bowen T, et al. Functional analysis of human promoter polymorphisms HUMAN MOLECULAR GENETICS. 2003 SEP 15; 12 (18): 2249-2254	6	87	3	28
#	Date / Author / Journal	LCS	GCS	LCR	CR
2491	2256 McGregor E, Dunn MJ Proteomics of heart disease HUMAN MOLECULAR GENETICS. 2003 OCT 15; 12: R135-R144	3	35	5	104
2492	2338 Lingaas F, Comstock KE, Kirkness EF, Sorensen A, Aarskaug T, et al. A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog HUMAN MOLECULAR GENETICS. 2003 DEC 1; 12 (23): 3043-3053	1	65	1	48
2493	2573 Slaugenhaupt SA, Mull J, Leyne M, Cuajungco MP, Gill SP, et al. Rescue of a human mRNA splicing defect by the plant cytokinin kinetin HUMAN MOLECULAR GENETICS. 2004 FEB 15; 13 (4): 429-436	0	41	2	37
2494	2622 Stoilov P, Daoud R, Nayler O, Stamm S Human tra2-beta1 autoregulates its protein concentration by influencing alternative splicing of its pre-mRNA HUMAN MOLECULAR GENETICS. 2004 MAR 1; 13 (5): 509-524	2	52	8	73
2495	2730 Wang QL, Chen SM, Esumi N, Swain PK, Haines HS, et al. QRX, a novel homeobox gene, modulates photoreceptor gene expression HUMAN MOLECULAR GENETICS. 2004 MAY 15; 13 (10): 1025-1040	0	22	3	73
2496	3179 Bhangale TR, Rieder MJ, Livingston RJ, Nickerson DA Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes HUMAN MOLECULAR GENETICS. 2005 JAN 1; 14 (1): 59-69	4	41	6	69
2497	3273 Alfano G, Vitiello C, Caccioppoli C, Caramico T, Carola A, et al. Natural antisense transcripts associated with genes involved in eye development HUMAN MOLECULAR GENETICS. 2005 APR 1; 14 (7): 913-923	1	33	5	39
2498	3413 Kryukov GV, Schmidt S, Sunyaev S Small fitness effect of mutations in highly conserved non-coding regions HUMAN MOLECULAR GENETICS. 2005 AUG 1; 14 (15): 2221-2229	3	30	9	41
2499	3442 Sironi M, Menozzi G, Comi GP, Cagliani R, Bresolin N, et al. Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequences HUMAN MOLECULAR GENETICS. 2005 SEP 1; 14 (17): 2533-2546	1	32	10	87
2500	3784 Gorlov IP, Kimmel M, Amos CI Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome HUMAN MOLECULAR GENETICS. 2006 APR 1; 15 (7): 1143-1150	0	3	5	53

Date / Author / Journal

LCS

GCS

LCR

2401

3327 Dalla E, Mignone F, Verardo R, Marchionni L, Marzinotto S, et al.

Discovery of 342 putative new genes from the analysis of 5 '-end-sequenced full-length-enriched cDNA human transcripts

GENOMICS. 2005 JUN; 85 (6): 739-751

2402

3400 Ge XJ, Yamamoto S, Tsutsumi S, Midorikawa Y, Ihara S, et al.

Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues

GENOMICS. 2005 AUG; 86 (2): 127-141

2403

3465 Hancock DK, Tully LA, Levin BC

A Standard Reference Material to determine the sensitivity of techniques for detecting low-frequency mutations, SNPs, and heteroplasmies in mitochondrial DNA

GENOMICS. 2005 OCT; 86 (4): 446-461

2404

3533 Puente XS, Gutierrez-Fernandez A, Ordonez GR, Hillier LDW, Lopez-Otin C

Comparative genomic analysis of human and chimpanzee proteases

GENOMICS. 2005 DEC; 86 (6): 638-647

2405

3534 Meyers SN, Rogatcheva MB, Larkin DM, Yerle M, Milan D, et al.

Piggy-BACing the human genome - II. A high-resolution, physically anchored, comparative map of the porcine autosomes

GENOMICS. 2005 DEC; 86 (6): 739-+

2406

3657 Li JG, Liljedahl U, Heng CK

Tag/anti-tag liquid-phase primer extension array: A flexible and versatile genotyping platform

GENOMICS. 2006 JAN; 87 (1): 151-157

2407

3774 Brzoska PM, Brown C, Cassel M, Ceccardi T, Di Francisco V, et al.

An efficient and high-throughput approach for experimental validation of novel human gene predictions

GENOMICS. 2006 APR; 87 (4): 437-445

2408

3803 Feltus FA, Lee EK, Costello JF, Plass C, Vertino PM

DNA motifs associated with aberrant CpG island methylation

GENOMICS. 2006 MAY; 87 (5): 572-579

2409

3941 Bjarnadottir TK, Gloriam DE, Hellstrand SH, Kristiansson H, Fredriksson R, et al.

Comprehensive repertoire and phylogenetic analysis of the G protein-coupled receptors in human and mouse

GENOMICS. 2006 SEP; 88 (3): 263-273

2410

4012 Haitina T, Lindblom J, Renstrom T, Fredriksson R

Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system

GENOMICS. 2006 DEC; 88 (6): 779-790

Date / Author / Journal

LCS

GCS

LCR

2411

4113 Vanhoutteghem A, Djian P

The human basonuclin 2 gene has the potential to generate nearly 90,000 mRNA isoforms encoding over 2000 different proteins

GENOMICS. 2007 JAN; 89 (1): 44-58

2412

4177 Lamesch P, Li N, Milstein S, Fan CY, Hao T, et al.

h0RFeome v3.1: A resource of human open reading frames representing over 10,000 human genes

GENOMICS. 2007 MAR; 89 (3): 307-315

2413

4284 Torkamani A, Schork NJ

Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family

GENOMICS. 2007 JUL; 90 (1): 49-58

2414

4328 Langille MGI, Clark DV

Parent genes of retrotransposition-generated gene duplicates in Drosophila melanogaster have distinct expression profiles

GENOMICS. 2007 SEP; 90 (3): 334-343

2415

4542 Tan K, Tegner J, Ravasi T

Integrated approaches to uncovering transcription regulatory networks in mammalian cells

GENOMICS. 2008 MAR; 91 (3): 219-231

132

2416

4543 Ji XL, Zhao SY

DA and Xiao-two giant and composite LTR-retrotransposon-like elements identified in the human genome

GENOMICS. 2008 MAR; 91 (3): 249-258

2417

4652 Louro R, El-Jundi T, Nakaya HI, Reis EM, Verjovski-Almeida S

Conserved tissue expression signatures of intronic noncoding RNAs transcribed from human and mouse loci

GENOMICS. 2008 JUL; 92 (1): 18-25

2418

4676 Zhang DF, Yang QY, Ding Y, Cao XF, Xue YB, et al.

Cytological characterization of the tandem repetitive sequences and their methylation status in the Antirrhinum majus genome

GENOMICS. 2008 AUG; 92 (2): 107-114

2419

4701 Lee TM, Lipovich L

Structural differences of orthologous genes: Insights from human-primate comparisons

GENOMICS. 2008 SEP; 92 (3): 134-143

2420

4761 Morozova O, Marra MA

Applications of next-generation sequencing technologies in functional genomics

GENOMICS. 2008 NOV; 92 (5): 255-264

111

Date / Author / Journal

LCS

GCS

LCR

2421

4893 Pettersson E, Lundeberg J, Ahmadian A

Generations of sequencing technologies

GENOMICS. 2009 FEB; 93 (2): 105-111

2422

4967 Wilkening S, Chen BW, Bermejo JL, Canzian F

Is there still a need for candidate gene approaches in the era of genome-wide association studies?

GENOMICS. 2009 MAY; 93 (5): 415-419

2423

894 Hoffmann W, Latza U, Ahrens W, Greiser KH, Kroke A, et al.

Biological markers in epidemiology: Concepts, applications, perspectives (Part II)

GESUNDHEITSWESEN. 2002 MAR; 64 (3): 145-152

2424

1944 Wilson VA, Gallagher JT, Merry CLR

Heparan sulfate 2-O-sulfotransferase (Hs2st) and mouse development

GLYCOCONJUGATE JOURNAL. 2003 MAY-JUN; 19 (4-5): 347-354

2425

4066 Wigglesworth MJ, Wolfe LA, Wise A

Orphan seven transmembrane receptor screening

GPCRS: FROM DEORPHANIZATION TO LEAD STRUCTURE IDENTIFICATION. 2007; 2: 105-143

195

2426

3103 Breimer E, Goldberg M, Hollinger D, Lim D

Discovering optimization algorithms through automated learning

GRAPHS AND DISCOVERY. 2005; 69: 7-25

2427

3104 Trejo JL, Carro E, Burks DJ

Experimental models for understanding the role of insulin-like growth factor-I and its receptor during development

GROWTH HORMONE/INSULIN-LIKE GROWTH FACTOR AXIS DURING DEVELOPMENT. 2005; 567: 27-53

116

2428

4404 Park NH, Song H, Chung YH

Molecular Pathogenesis of Hepatitis-B-virus-associated Hepatocellular Carcinoma

GUT AND LIVER. 2007 DEC; 1 (2): 101-117

132

2429

3105 te Velde ER

Is women's emancipation still compatible with reproduction in this century?

GYNAECOLOGY, OBSTETRICS, AND REPRODUCTIVE MEDICINE IN DAILY PRACTICE. 2005; 1279: 58-67

2430

3606 Guo SW

Association of endometriosis risk and genetic polymorphisms involving sex steroid biosynthesis and their receptors: A meta-analysis

GYNECOLOGIC AND OBSTETRIC INVESTIGATION. 2006; 61 (2): 90-105

Date / Author / Journal

LCS

GCS

LCR

2431

1701 Gray JW, Suzuki S, Kuo WL, Polikoff D, Deavers M, et al.

Specific keynote: Genome copy number abnormalities in ovarian cancer

GYNECOLOGIC ONCOLOGY. 2003 JAN; 88 (1): S16-S21

2432

2553 Ferguson SE, Olshen AB, Viale A, Awtrey CS, Barakat RR, et al.

Gene expression profiling of tamoxifen-associated uterine cancers: evidence for two molecular classes of endometrial carcinoma

GYNECOLOGIC ONCOLOGY. 2004 FEB; 92 (2): 719-725

2433

4178 Walsh CS, Miller CW, Karlan BY, Koeffler HP

Association between a functional single nucleotide polyrnorphism in the MDM2 gene and sporadic endometrial cancer risk

GYNECOLOGIC ONCOLOGY. 2007 MAR; 104 (3): 660-664

2434

3194 Corral J, Vicente V, Carrell RW

Thrombosis as a conformational disease

HAEMATOLOGICA. 2005 FEB; 90 (2): 238-246

2435

3365 Berntorp E, Astermark J, Donfield SM, Nelson GW, Oldenburg J, et al.

Haemophilia Inhibitor Genetics Study - evaluation of a model for studies of complex diseases using linkage and association methods

HAEMOPHILIA. 2005 JUL; 11 (4): 427-429

2436

4013 [Anon]

Guiding regulatory reform in reproduction and genetics

HARVARD LAW REVIEW. 2006 DEC; 120 (2): 574-596

2437

186 Sklar P

The genomic approach to candidate genes

HARVARD REVIEW OF PSYCHIATRY. 2001 JUL-AUG; 9 (4): 197-207

2438

3727 Scolnick EM, Petryshen T, Sklar P

Schizophrenia: Do the genetics and neurobiology of neuregulin provide a pathogenesis model?

HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 64-77

2439

3728 Roffman JL, Weiss AP, Goff DC, Rauch SL, Weinberger DR

Neuroimaging-genetic paradigms: A new approach to investigate the pathophysiology and treatment of cognitive deficits in schizophrenia

HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 78-91

126

2440

2077 Amundson SA, Fornace AJ

Monitoring human radiation exposure by gene expression profiling: Possibilities and pitfalls

HEALTH PHYSICS. 2003 JUL; 85 (1): 36-42

Date / Author / Journal

2441

Are DNA patents bad for medicine?

HEALTH POLICY. 2003 AUG; 65 (2): 181-197

2442

1508 Shackel NA, Gorrell MD, McCaughan GW

Gene array analysis and the liver

HEPATOLOGY. 2002 DEC; 36 (6): 1313-1325

121

2443

1879 Thorgeirsson SS

Hunting for tumor suppressor genes in liver cancer

HEPATOLOGY. 2003 APR; 37 (4): 739-741

2444

2183 Shackel NA, McGuinness PH, Abbott CA, Gorrell MD, McCaughan GW

Novel differential gene expression in human cirrhosis detected by suppression subtractive hybridization

HEPATOLOGY. 2003 SEP; 38 (3): 577-588

2445

2646 Zhang DY, Sabla G, Shivakumar P, Tiao G, Sokol RJ, et al.

Coordinate expression of regulatory genes differentiates embryonic and perinatal forms of biliary atresia

HEPATOLOGY. 2004 APR; 39 (4): 954-962

2446

4014 Juran BD, Lazaridis KN

Genomics and complex liver disease: Challenges and opportunities

HEPATOLOGY. 2006 DEC; 44 (6): 1380-1390

2447

1945 Sverdlov ED

DNA in a cell: From a molecular icon to the problem of "what is life?"

HERALD OF THE RUSSIAN ACADEMY OF SCIENCES. 2003 MAY-JUN; 73 (3): 262-269

2448

4285 Portin P

Evolution of man in the light of molecular genetics: a review. Part I. Our evolutionary history and genomics

HEREDITAS. 2007 JUL; 144 (3): 80-95

130

2449

5045 Sato K, Nankaku N, Takeda K

A high-density transcript linkage map of barley derived from a single population

HEREDITY. 2009 AUG; 103 (2): 110-117

2450

34 Prestegard JH

High resolution NMR of biomolecules

HIGH MAGNETIC FIELDS. 2001; 595: 426-434

Date / Author / Journal

LCS

GCS

LCR

2451

671 Alur R, Belta C, Ivancic N, Kumar V, Rubin H, et al.

Visual programming for modeling and simulation of biomolecular regulatory networks

HIGH PERFORMANCE COMPUTING - HIPC 2002, PROCEEDINGS. 2002; 2552: 702-712

2452

1260 Roix J, Misteli T

Genomes, proteomes, and dynamic networks in the cell nucleus

HISTOCHEMISTRY AND CELL BIOLOGY. 2002 AUG; 118 (2): 105-116

2453

965 Finta C, Warner SC, Zaphiropoulos PG

Intergenic mRNAs. Minor gene products or tools of diversity?

HISTOLOGY AND HISTOPATHOLOGY. 2002 APR; 17 (2): 677-682

2454

2184 Haas DW, Wilkinson GR, Kuritzkes DR, Richman DD, Nicotera J, et al.

A multi-investigator/institutional DNA bank for AIDS-related human genetic studies: AACTG Protocol A5128

HIV CLINICAL TRIALS. 2003 SEP-OCT; 4 (5): 287-300

2455

5026 Basham RJ, Richardson DM, Sutcliffe CB, Haas DW

Effect of HIV-1 Infection on Human DNA Yield from Saliva

HIV CLINICAL TRIALS. 2009 JUL-AUG; 10 (4): 282-285

2456

35 Bouillon R

The future of endocrinology and the endocrinologist of the future

HORMONE RESEARCH. 2001; 56: 98-105

2457

1630 Polychronakos C

Impact of the human genome project on pediatric endocrinology

HORMONE RESEARCH. 2003; 59 (2): 55-65

2458

672 Pucci-Minafra I, Fontana S, Cancemi P, Alaimo G, Minafra S

Proteomic patterns of cultured breast cancer cells and epithelial mammary cells

2459

4443 Ribeiro EO, Walter MEMT, Costa MM, Togawa R, Pappas G

p2pBIOFOCO: Proposing a Peer-to-Peer System for Distributed BLAST Execution

HPCC 2008: 10TH IEEE INTERNATIONAL CONFERENCE ON HIGH PERFORMANCE COMPUTING AND COMMUNICATIONS, PROCEEDINGS. 2008; : 594-601

2460

2133 Eckhardt RB

Polymorphisms past and present

HUMAN BIOLOGY. 2003 AUG; 75 (4): 559-575

Date / Author / Journal

2461

On making behavioral genetics truly developmental

HUMAN DEVELOPMENT. 2003 NOV-DEC; 46 (6): 337-355

2462

230 Willett-Brozick JE, Savul SA, Richey LE, Baysal BE

Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation

HUMAN GENETICS. 2001 AUG; 109 (2): 216-223

2463

371 Spyrou G, Wilson W, Padilla CA, Holmgren A, Miranda-Vizuete A

A genome-wide survey of human thioredoxin and glutaredoxin family pseudogenes

HUMAN GENETICS. 2001 OCT; 109 (4): 429-439

2464

823 Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson JT, Syrjakoski K, et al.

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

HUMAN GENETICS. 2002 FEB; 110 (2): 111-121

2465

1509 Amsellem S, Briffaut D, Carrie A, Rabes JP, Girardet JP, et al.

Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia

HUMAN GENETICS. 2002 DEC; 111 (6): 501-510

2466

1702 Speckman RA, Daw JAW, Helms C, Duan SH, Cao L, et al.

Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility

HUMAN GENETICS. 2003 JAN; 112 (1): 34-41

2467

1946 Buzdin A, Ustyugova S, Gogvadze E, Lebedev Y, Hunsmann G, et al.

Genome-wide targeted search for human specific and polymorphic L1 integrations

HUMAN GENETICS. 2003 MAY; 112 (5-6): 527-533

2468

3882 Tang H, Jorgenson E, Gadde M, Kardia SLR, Rao DC, et al.

Racial admixture and its impact on BMI and blood pressure in African and Mexican Americans

HUMAN GENETICS. 2006 JUL; 119 (6): 624-633

2469

4114 Zhang XZ, Mahmudi-Azer S, Connett JE, Anthonisen NR, He JQ, et al.

Association of Hck genetic polymorphisms with gene expression and COPD

HUMAN GENETICS. 2007 JAN; 120 (5): 681-690

2470

4894 Zhang W, Duan SW, Bleibel WK, Wisel SA, Huang RS, et al.

Identification of common genetic variants that account for transcript isoform variation between human populations

HUMAN GENETICS. 2009 FEB; 125 (1): 81-93

Date / Author / Journal

2471

Transposable elements in disease-associated cryptic exons

HUMAN GENETICS. 2010 FEB; 127 (2): 135-154

158

2472

673 DeWan AT, Parrado AR, Matise TC, Leal SM

Map error reduction: Using genetic and sequence-based physical maps to order closely linked markers

HUMAN HEREDITY. 2002; 54 (1): 34-44

2473

2416 Halldorsson BV, Istrail S, De La Vega FM

Optimal selection of SNP markers for disease association studies

HUMAN HEREDITY. 2004; 58 (3-4): 190-202

2474

395 Goodstadt L, Ponting CR

Sequence variation and disease in the wake of the draft human genome

HUMAN MOLECULAR GENETICS. 2001 OCT 1; 10 (20): 2209-2214

2475

396 Horvath JE, Bailey JA, Locke DP, Eichler EE

Lessons from the human genome: transitions between euchromatin and heterochromatin

HUMAN MOLECULAR GENETICS. 2001 OCT 1; 10 (20): 2215-2223

2476

397 Miller MP, Kumar S

Understanding human disease mutations through the use of interspecific genetic variation

HUMAN MOLECULAR GENETICS. 2001 OCT 2; 10 (21): 2319-2328

115

2477

478 Takai D, Gonzales FA, Tsai YC, Thayer MJ, Jones PA

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

HUMAN MOLECULAR GENETICS. 2001 NOV 1; 10 (23): 2619-2626

2478

769 Watanabe Y, Fujiyama A, Ichiba Y, Hattori M, Yada T, et al.

Chromosome-wide assessment of replication timing for human chromosomes 11q and 21q: disease-related genes in timing-switch regions

HUMAN MOLECULAR GENETICS. 2002 JAN 1; 11 (1): 13-21

2479

993 Thaung C, West K, Clark BJ, McKie L, Morgan JE, et al.

Novel ENU-induced eye mutations in the mouse: models for human eye disease

HUMAN MOLECULAR GENETICS. 2002 APR 1; 11 (7): 755-767

2480

1276 Coleman SL, Buckland PR, Hoogendoorn B, Guy C, Smith K, et al.

Experimental analysis of the annotation of promoters in the public database

HUMAN MOLECULAR GENETICS. 2002 AUG 1; 11 (16): 1817-1821

Date / Author / Journal

LCS

GCS

LCR

2481

1277 Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, et al.

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

HUMAN MOLECULAR GENETICS. 2002 AUG 1; 11 (16): 1887-1898

2482

1352 Saarela J, Fejzo MS, Chen D, Finnila S, Parkkonen M, et al.

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24

HUMAN MOLECULAR GENETICS. 2002 SEP 15; 11 (19): 2257-2267

2483

1353 Wang PJ, Page DC

Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis

HUMAN MOLECULAR GENETICS. 2002 SEP 15; 11 (19): 2341-2346

2484

1396 Stamm S

Signals and their transduction pathways regulating alternative splicing: a new dimension of the human genome

HUMAN MOLECULAR GENETICS. 2002 OCT 1; 11 (20): 2409-2416

109

101

2485

1784 Duan JB, Wainwright MS, Comeron JM, Saitou N, Sanders AR, et al.

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

HUMAN MOLECULAR GENETICS. 2003 FEB 1; 12 (3): 205-216

240

2486

1902 Emes RD, Goodstadt L, Winter EE, Ponting CP

Comparison of the genomes of human and mouse lays the foundation of genome zoology

HUMAN MOLECULAR GENETICS. 2003 APR 1; 12 (7): 701-709

119

2487

2034 Gong ML, Zhang HY, Schulz H, Lee YA, Sun K, et al.

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p

HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1273-1277

2488

2035 Semenova E, Wang XF, Jablonski MM, Levorse J, Tilghman SM

An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina

HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1301-1312

2489

2036 Ejima Y, Yang LC

Trans mobilization of genomic DNA as a mechanism for retrotransposon-mediated exon shuffling

HUMAN MOLECULAR GENETICS. 2003 JUN 1; 12 (11): 1321-1328

2490

2209 Hoogendoorn B, Coleman SL, Guy CA, Smith K, Bowen T, et al.

Functional analysis of human promoter polymorphisms

HUMAN MOLECULAR GENETICS. 2003 SEP 15; 12 (18): 2249-2254

Date / Author / Journal

LCS

GCS

LCR

2491

2256 McGregor E, Dunn MJ

Proteomics of heart disease

HUMAN MOLECULAR GENETICS. 2003 OCT 15; 12: R135-R144

104

2492

2338 Lingaas F, Comstock KE, Kirkness EF, Sorensen A, Aarskaug T, et al.

A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog

HUMAN MOLECULAR GENETICS. 2003 DEC 1; 12 (23): 3043-3053

2493

2573 Slaugenhaupt SA, Mull J, Leyne M, Cuajungco MP, Gill SP, et al.

Rescue of a human mRNA splicing defect by the plant cytokinin kinetin

HUMAN MOLECULAR GENETICS. 2004 FEB 15; 13 (4): 429-436

2494

2622 Stoilov P, Daoud R, Nayler O, Stamm S

Human tra2-beta1 autoregulates its protein concentration by influencing alternative splicing of its pre-mRNA

HUMAN MOLECULAR GENETICS. 2004 MAR 1; 13 (5): 509-524

2495

2730 Wang QL, Chen SM, Esumi N, Swain PK, Haines HS, et al.

QRX, a novel homeobox gene, modulates photoreceptor gene expression

HUMAN MOLECULAR GENETICS. 2004 MAY 15; 13 (10): 1025-1040

2496

3179 Bhangale TR, Rieder MJ, Livingston RJ, Nickerson DA

Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes

HUMAN MOLECULAR GENETICS. 2005 JAN 1; 14 (1): 59-69

2497

3273 Alfano G, Vitiello C, Caccioppoli C, Caramico T, Carola A, et al.

Natural antisense transcripts associated with genes involved in eye development

HUMAN MOLECULAR GENETICS. 2005 APR 1; 14 (7): 913-923

2498

3413 Kryukov GV, Schmidt S, Sunyaev S

Small fitness effect of mutations in highly conserved non-coding regions

HUMAN MOLECULAR GENETICS. 2005 AUG 1; 14 (15): 2221-2229

2499

3442 Sironi M, Menozzi G, Comi GP, Cagliani R, Bresolin N, et al.

Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequences

HUMAN MOLECULAR GENETICS. 2005 SEP 1; 14 (17): 2533-2546

2500

3784 Gorlov IP, Kimmel M, Amos CI

Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome

HUMAN MOLECULAR GENETICS. 2006 APR 1; 15 (7): 1143-1150

The sequence of the human genome (Venter) The papers citing Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, et al. "The sequence of the human genome." SCIENCE. 2001 FEB 16; 291 (5507): 1304	Historiographs	Glossary HistCite Guide About Grand Totals: LCS 18020, GCS 180410, CR 319862 Collection span: 2000 - 2010
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