HistCite - Initial sequencing and analysis of the human genome (Lander)

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#	Date / Author / Journal	LCS	GCS	LCR	CR
3401	5326 de Bustos C, de Stahl TD, Piotrowski A, Mantripragada KK, Buckley PG, et al. Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH GENOMICS. 2006 AUG; 88 (2): 152-162	0	8	10	46
3402	5362 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	4	29	13	40
3403	5363 Hutter B, Helms V, Paulsen M Tandem repeats in the CpG islands of imprinted genes GENOMICS. 2006 SEP; 88 (3): 323-332	3	22	8	54
3404	5418 Wu CC, Wang SJ, Zhang HB Interactions among genomic structure, function, and evolution revealed by comprehensive analysis of the Arabidopsis thaliana genome GENOMICS. 2006 OCT; 88 (4): 394-406	0	2	8	35
3405	5499 Mazzarelli JM, White P, Gorski R, Brestelli J, Pinney DF, et al. Novel genes identified by manual annotation and microarray expression analysis in the pancreas GENOMICS. 2006 DEC; 88 (6): 752-761	0	2	8	44
3406	5640 Sasaki T, Shimizu A, Ishikawa SK, Imai S, Asakawa S, et al. The DNA sequence of medaka chromosome LG22 GENOMICS. 2007 JAN; 89 (1): 124-133	1	6	11	33
3407	5641 Keebaugh AC, Sullivan RT, Thomas JW, NISC Compartive Sequencing Program Gene duplication and inactivation in the HPRT gene family GENOMICS. 2007 JAN; 89 (1): 134-142	0	0	13	50
3408	5696 Osoegawa K, Vessere GM, Shu CL, Hoskins RA, Abad JP, et al. BAC clones generated from sheared DNA GENOMICS. 2007 FEB; 89 (2): 291-299	2	4	7	37
3409	5742 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	14	39
3410	5945 Torkamani A, Schork NJ Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family GENOMICS. 2007 JUL; 90 (1): 49-58	2	9	6	42
#	Date / Author / Journal	LCS	GCS	LCR	CR
3411	5946 Cordaux R, Srikanta D, Lee J, Stoneking M, Batzer MA In search of polymorphic Alu insertions with restricted geographic distributions GENOMICS. 2007 JUL; 90 (1): 154-158	3	3	14	27
3412	5982 Ramos KS, He Q, Kalbfleisch T, Montoya-Durango DE, Teneng I, et al. Computational and biological inference of gene regulatory networks of the LINE-1 retrotransposon GENOMICS. 2007 AUG; 90 (2): 176-185	0	2	14	45
3413	6371 Tan K, Tegner J, Ravasi T Integrated approaches to uncovering transcription regulatory networks in mammalian cells GENOMICS. 2008 MAR; 91 (3): 219-231	1	5	12	132
3414	6372 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	17	39
3415	6562 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	15	46
3416	6563 Simmen MW Genome-scale relationships between cytosine methylation and dinucleotide abundances in animals GENOMICS. 2008 JUL; 92 (1): 33-40	0	5	7	44
3417	6683 Rosenkranz R, Borodina T, Lehrach H, Himmelbauer H Characterizing the mouse ES cell transcriptome with Illumina sequencing GENOMICS. 2008 OCT; 92 (4): 187-194	2	10	3	37
3418	6729 Morozova O, Marra MA Applications of next-generation sequencing technologies in functional genomics GENOMICS. 2008 NOV; 92 (5): 255-264	3	35	10	111
3419	6885 Benovoy D, Drouin G Ectopic gene conversions in the human genome GENOMICS. 2009 JAN; 93 (1): 27-32	0	5	3	44
3420	6927 Pettersson E, Lundeberg J, Ahmadian A Generations of sequencing technologies GENOMICS. 2009 FEB; 93 (2): 105-111	1	12	8	40
#	Date / Author / Journal	LCS	GCS	LCR	CR
3421	6957 Huang J, Zhang KW, Shen Y, Huang ZJ, Li M, et al. Identification of a high frequency transposon induced by tissue culture, nDaiZ, a member of the hAT family in rice GENOMICS. 2009 MAR; 93 (3): 274-281	0	0	8	40
3422	7048 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	5	20
3423	7049 Ma XJ, Li-Ling J, Huang QL, Chen X, Hou L, et al. Systematic analysis of alternative promoters correlated with alternative splicing in human genes GENOMICS. 2009 MAY; 93 (5): 420-425	0	0	18	47
3424	7127 Marchani EE, Xing JC, Witherspoon DJ, Jorde LB, Rogers AR Estimating the age of retrotransposon subfamilies using maximum likelihood GENOMICS. 2009 JUL; 94 (1): 78-82	0	0	15	33
3425	7323 Cruickshanks HA, Tufarelli C Isolation of cancer-specific chimeric transcripts induced by hypomethylation of the LINE-1 antisense promoter GENOMICS. 2009 DEC; 94 (6): 397-406	0	0	15	43
3426	6223 Clark LA, Wahl JM, Rees CA, Strain GM, Cargill EJ, et al. Canine SINEs and their effects on phenotypes of the domestic dog GENOMICS OF DISEASE. 2008; : 79-87	0	1	7	33
3427	1077 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
3428	1752 Willer T, Amselgruber W, Deutzmann R, Strahl S Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids GLYCOBIOLOGY. 2002 NOV; 12 (11): 771-783	0	47	1	59
3429	2391 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
3430	807 Crocker PR, Zhang JQ New I-type lectins of the CD33-related siglec subgroup identified through genomics GLYCOGENOMICS: THE IMPACT OF GENOMICS AND INFORMATICS ON GLYCOBIOLOGY. 2002; (69): 83-94	0	2	5	62
#	Date / Author / Journal	LCS	GCS	LCR	CR
3431	5591 Wigglesworth MJ, Wolfe LA, Wise A Orphan seven transmembrane receptor screening GPCRS: FROM DEORPHANIZATION TO LEAD STRUCTURE IDENTIFICATION. 2007; 2: 105-143	0	0	7	195
3432	6886 Gutierrez GR, de Roos B Dietary fatty acids affecting hepatic metabolism and atherosclerosis - mechanisms unravelled using a proteomics approach GRASAS Y ACEITES. 2009 JAN-MAR; 60 (1): 28-32	0	0	6	40
3433	4063 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
3434	2392 Thomas G, Cann H Irruption of genomics in the search for disease related genes GUT. 2003 MAY; 52: II1-II5	0	0	4	27
3435	664 Hallek M, Buening H, Ried M, Hacker U, Kurzeder C, et al. Basics of gene therapy. Principles and development status GYNAKOLOGE. 2001 DEC; 34 (12): 1182-+	0	0	2	17
3436	3061 Taylor RN The future of endometriosis research: Genomics and proteomics? GYNECOLOGIC AND OBSTETRIC INVESTIGATION. 2004; 57 (1): 47-49	0	3	2	26
3437	2069 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	3	70
3438	2644 DiSaia PJ, Bloss JD Treatment of ovarian cancer: new strategies GYNECOLOGIC ONCOLOGY. 2003 AUG; 90 (2): S24-S32	0	20	1	48
3439	6838 Oppelt P, Strick R, Strissel PL, Winzierl K, Beckmann MW, et al. Expression of the human endogenous retroviruse-W envelope gene syncytin in endometriosis lesions GYNECOLOGICAL ENDOCRINOLOGY. 2009; 25 (11): 741-747	0	0	2	19
3440	6462 Dierlamm J, Penas EMM, Bentink S, Wessendorf S, Berger H, et al. Gain of chromosome region 18q21 including the MALT1 gene is associated with the activated B-cell-like gene expression subtype and increased BCL2 gene dosage and protein expression in diffuse large B-cell lymphoma HAEMATOLOGICA-THE HEMATOLOGY JOURNAL. 2008 MAY; 93 (5): 688-696	1	6	2	49
#	Date / Author / Journal	LCS	GCS	LCR	CR
3441	4484 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	3	23
3442	229 Sklar P The genomic approach to candidate genes HARVARD REVIEW OF PSYCHIATRY. 2001 JUL-AUG; 9 (4): 197-207	0	0	2	64
3443	5025 Potash JB Carving chaos: Genetics and the classification of mood and psychotic syndromes HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 47-63	0	28	2	152
3444	5026 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	4	74
3445	5027 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	5	126
3446	2560 Amundson SA, Fornace AJ Monitoring human radiation exposure by gene expression profiling: Possibilities and pitfalls HEALTH PHYSICS. 2003 JUL; 85 (1): 36-42	1	18	2	36
3447	289 Komajda M, Charron P How will the human genome project change cardiovascular medicine? HEART. 2001 AUG; 86 (2): 123-124	0	2	1	12
3448	1981 Christensen UB, Pedersen EB Intercalating nucleic acids with pyrene nucleotide analogues as next-nearest neighbors for excimer fluorescence detection of single-point mutations under nonstringent hybridization conditions HELVETICA CHIMICA ACTA. 2003; 86 (6): 2090-2097	1	35	1	26
3449	2239 Bataller R, North KE, Brenner DA Genetic polymorphisms and the progression of liver fibrosis: A critical appraisal HEPATOLOGY. 2003 MAR; 37 (3): 493-503	1	108	4	115
3450	2311 Thorgeirsson SS Hunting for tumor suppressor genes in liver cancer HEPATOLOGY. 2003 APR; 37 (4): 739-741	0	8	5	23
#	Date / Author / Journal	LCS	GCS	LCR	CR
3451	5500 Juran BD, Lazaridis KN Genomics and complex liver disease: Challenges and opportunities HEPATOLOGY. 2006 DEC; 44 (6): 1380-1390	0	11	6	84
3452	5788 Shin HJ, Anzai N, Enomoto A, He X, Kim DK, et al. Novel liver-specific organic anion transporter OAT7 that operates the exchange of sulfate conjugates for short chain fatty acid butyrate HEPATOLOGY. 2007 APR; 45 (4): 1046-1055	0	17	2	46
3453	2393 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	8	29
3454	5947 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	26	130
3455	2156 Hughes AL Comparative genomics - Genomes of mice and men HEREDITY. 2003 FEB; 90 (2): 115-116	0	0	3	8
3456	3452 Bofkin L, Whelan S Functional needles in a genomic haystack HEREDITY. 2004 MAY; 92 (5): 363-364	0	0	3	5
3457	5697 Leitch AR Conserved gene order belies rapid genome turnover - The dynamic interplay between genomic DNA and the outside world HEREDITY. 2007 FEB; 98 (2): 61-62	0	2	2	20
3458	7242 Sorek R When new exons are born HEREDITY. 2009 OCT; 103 (4): 279-280	0	0	5	8
3459	32 Prestegard JH High resolution NMR of biomolecules HIGH MAGNETIC FIELDS. 2001; 595: 426-434	0	2	3	21
3460	6839 Muotri AR, Zhao C, Marchetto MCN, Gage FH Environmental Influence on L1 Retrotransposons in the Adult Hippocampus HIPPOCAMPUS. 2009; 19 (10): 1002-1007	0	0	9	32
#	Date / Author / Journal	LCS	GCS	LCR	CR
3461	1536 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	4	79
3462	1153 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
3463	4843 Kubicek S, Schotta G, Lachner M, Sengupta R, Kohlmaier A, et al. The role of histone modifications in epigenetic transitions during normal and perturbed development HISTONE CODE AND BEYOND: NEW APPROACHES TO CANCER THERAPY. 2006; 57: 1-27	0	4	3	91
3464	808 Chambers FM, Brain SA Paradigm shifts in late-Holocene climatology? HOLOCENE. 2002; 12 (2): 239-249	0	2	1	112
3465	1982 Curnoe D, Thorne A Number of ancestral human species: a molecular perspective HOMO-JOURNAL OF COMPARATIVE HUMAN BIOLOGY. 2003; 53 (3): 201-224	0	13	2	138
3466	1983 Polychronakos C Impact of the human genome project on pediatric endocrinology HORMONE RESEARCH. 2003; 59 (2): 55-65	1	3	6	44
3467	809 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	1	24	2	18
3468	4844 Weber J, Futterer C, Gowri S, Attia R, Viovy JL Towards a microfluidic chip for unknown mutation detection and genotyping HOUILLE BLANCHE-REVUE INTERNATIONALE DE L EAU. 2006; (5): 40-44	0	0	2	9
3469	4845 Weber J, Futterer C, Gowri S, Attia R, Viovy JL Towards a microfluidic chip for unknown mutation detection and genotyping HOUILLE BLANCHE-REVUE INTERNATIONALE DE L EAU. 2006; (6): 40-44	0	0	2	9
3470	6840 Iimura T, Denans N, Pourquie O ESTABLISHMENT OF HOX VERTEBRAL IDENTITIES IN THE EMBRYONIC SPINE PRECURSORS HOX GENES. 2009; 88: 201-+	0	0	5	159
#	Date / Author / Journal	LCS	GCS	LCR	CR
3471	6224 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
3472	1681 Stayner L, Toraason M, Hattis D Risk assessment at the crossroads of the 21st century: Opportunities and challenges for research HUMAN AND ECOLOGICAL RISK ASSESSMENT. 2002 OCT; 8 (6): 1195-1202	0	0	1	27
3473	3920 Devor EJ, Moffat-Wilson KA, Galbraith JJ LOC 390443 (RNase 9) on chromosome 14q11.2 is related to the RNase a superfamily and contains a unique amino-terminal preproteinlike sequence HUMAN BIOLOGY. 2004 DEC; 76 (6): 921-935	2	7	2	38
3474	4532 Mangeat B, Trono D Lentiviral vectors and antiretroviral intrinsic immunity HUMAN GENE THERAPY. 2005 AUG; 16 (8): 913-920	1	18	3	55
3475	290 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	6	21	2	47
3476	459 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	1	7	3	51
3477	665 Benjes SM, Morris CM A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22 HUMAN GENETICS. 2001 DEC; 109 (6): 628-637	0	0	1	51
3478	666 Kelberman D, Tyson J, Chandler DC, McInerney AM, Slee J, et al. Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome HUMAN GENETICS. 2001 DEC; 109 (6): 638-645	0	25	1	54
3479	990 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
3480	1823 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
#	Date / Author / Journal	LCS	GCS	LCR	CR
3481	2070 Knowles JW, Erickson LM, Guy VK, Sigel CS, Wilder JC, et al. Common variations in noncoding regions of the human natriuretic peptide receptor A gene have quantitative effects HUMAN GENETICS. 2003 JAN; 112 (1): 62-70	0	17	1	38
3482	2240 Sironi M, Pozzoli U, Cagliani R, Giorda R, Comi GP, et al. Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot HUMAN GENETICS. 2003 MAR; 112 (3): 272-288	3	16	1	54
3483	2394 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	16	18	9	27
3484	2561 Rothrock CR, Murgia A, Sartorato EL, Leonardi E, Wei SN, et al. Connexin 26 35delG does not represent a mutational hotspot HUMAN GENETICS. 2003 JUL; 113 (1): 18-23	0	20	1	22
3485	2562 Zhu LX, Swergold GD, Seldin MF Examination of sequence homology between human chromosome 20 and the mouse genome: intense conservation of many genomic elements HUMAN GENETICS. 2003 JUL; 113 (1): 60-70	2	9	5	25
3486	2645 van den Hurk JAJM, van de Pol DJR, Wissinger B, van Driel MA, Hoefsloot LH, et al. Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon HUMAN GENETICS. 2003 AUG; 113 (3): 268-275	3	13	3	51
3487	2848 Claverie-Martin F, Gonzalez-Acosta H, Flores C, Anton-Gamero M, Garcia-Nieto V De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease HUMAN GENETICS. 2003 NOV; 113 (6): 480-485	6	18	6	42
3488	3313 Timms KM, Wagner S, Samuels ME, Forbey K, Goldfine H, et al. A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree HUMAN GENETICS. 2004 MAR; 114 (4): 349-353	1	96	2	12
3489	3453 Langan JE, Cole CG, Huckle EJ, Byrne S, McRonald FE, et al. Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene HUMAN GENETICS. 2004 MAY; 114 (6): 534-540	0	13	3	17
3490	3454 Winter J, Lehmann T, Krauss S, Trockenbacher A, Kijas Z, et al. Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing HUMAN GENETICS. 2004 MAY; 114 (6): 541-552	4	10	3	24
#	Date / Author / Journal	LCS	GCS	LCR	CR
3491	3455 Hu FZ, Donfack J, Ahmed A, Dopico R, Johnson S, et al. Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14 HUMAN GENETICS. 2004 MAY; 114 (6): 562-572	0	6	2	19
3492	4143 Shaw CJ, Lupski JR Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms HUMAN GENETICS. 2005 JAN; 116 (1-2): 1-7	1	35	8	25
3493	4579 Chen JM, Stenson PD, Cooper DN, Ferec C A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease HUMAN GENETICS. 2005 SEP; 117 (5): 411-427	34	52	42	133
3494	4635 Leimkuhler S, Charcosset M, Latour P, Dorche C, Kleppe S, et al. Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase HUMAN GENETICS. 2005 OCT; 117 (6): 565-570	0	3	1	25
3495	4636 Eagle ARR, Hanson RL, Jiang WP, Han XL, Matters GL, et al. Meprin beta metalloprotease gene polymorphisms associated with diabetic nephropathy in the Pima Indians HUMAN GENETICS. 2005 OCT; 118 (1): 12-22	0	9	1	52
3496	4918 Hassan MJ, Santos RLP, Rafiq MA, Chahrour MH, Pham TL, et al. A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3 HUMAN GENETICS. 2006 JAN; 118 (5): 605-610	0	2	1	26
3497	5327 Santos RLP, Hassan MJ, Sikandar S, Lee K, Ali G, et al. DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2 HUMAN GENETICS. 2006 AUG; 120 (1): 85-92	1	4	1	21
3498	5836 Ali G, Chishti MS, Raza SI, John P, Ahmad W A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis HUMAN GENETICS. 2007 MAY; 121 (3-4): 319-325	0	16	4	34
3499	6022 Jackson EM, Shaikh TH, Gururangan S, Jones MC, Malkin D, et al. High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor HUMAN GENETICS. 2007 SEP; 122 (2): 117-127	0	8	3	43
3500	6326 Hassan MJ, Chishti MS, Jamal SM, Tariq M, Ahmad W A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2 HUMAN GENETICS. 2008 FEB; 123 (1): 77-82	1	2	2	27

Date / Author / Journal

LCS

GCS

LCR

3401

5326 de Bustos C, de Stahl TD, Piotrowski A, Mantripragada KK, Buckley PG, et al.

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH

GENOMICS. 2006 AUG; 88 (2): 152-162

3402

5362 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

3403

5363 Hutter B, Helms V, Paulsen M

Tandem repeats in the CpG islands of imprinted genes

GENOMICS. 2006 SEP; 88 (3): 323-332

3404

5418 Wu CC, Wang SJ, Zhang HB

Interactions among genomic structure, function, and evolution revealed by comprehensive analysis of the Arabidopsis thaliana genome

GENOMICS. 2006 OCT; 88 (4): 394-406

3405

5499 Mazzarelli JM, White P, Gorski R, Brestelli J, Pinney DF, et al.

Novel genes identified by manual annotation and microarray expression analysis in the pancreas

GENOMICS. 2006 DEC; 88 (6): 752-761

3406

5640 Sasaki T, Shimizu A, Ishikawa SK, Imai S, Asakawa S, et al.

The DNA sequence of medaka chromosome LG22

GENOMICS. 2007 JAN; 89 (1): 124-133

3407

5641 Keebaugh AC, Sullivan RT, Thomas JW, NISC Compartive Sequencing Program

Gene duplication and inactivation in the HPRT gene family

GENOMICS. 2007 JAN; 89 (1): 134-142

3408

5696 Osoegawa K, Vessere GM, Shu CL, Hoskins RA, Abad JP, et al.

BAC clones generated from sheared DNA

GENOMICS. 2007 FEB; 89 (2): 291-299

3409

5742 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

3410

5945 Torkamani A, Schork NJ

Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family

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

Date / Author / Journal

LCS

GCS

LCR

3411

5946 Cordaux R, Srikanta D, Lee J, Stoneking M, Batzer MA

In search of polymorphic Alu insertions with restricted geographic distributions

GENOMICS. 2007 JUL; 90 (1): 154-158

3412

5982 Ramos KS, He Q, Kalbfleisch T, Montoya-Durango DE, Teneng I, et al.

Computational and biological inference of gene regulatory networks of the LINE-1 retrotransposon

GENOMICS. 2007 AUG; 90 (2): 176-185

3413

6371 Tan K, Tegner J, Ravasi T

Integrated approaches to uncovering transcription regulatory networks in mammalian cells

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

132

3414

6372 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

3415

6562 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

3416

6563 Simmen MW

Genome-scale relationships between cytosine methylation and dinucleotide abundances in animals

GENOMICS. 2008 JUL; 92 (1): 33-40

3417

6683 Rosenkranz R, Borodina T, Lehrach H, Himmelbauer H

Characterizing the mouse ES cell transcriptome with Illumina sequencing

GENOMICS. 2008 OCT; 92 (4): 187-194

3418

6729 Morozova O, Marra MA

Applications of next-generation sequencing technologies in functional genomics

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

111

3419

6885 Benovoy D, Drouin G

Ectopic gene conversions in the human genome

GENOMICS. 2009 JAN; 93 (1): 27-32

3420

6927 Pettersson E, Lundeberg J, Ahmadian A

Generations of sequencing technologies

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

Date / Author / Journal

LCS

GCS

LCR

3421

6957 Huang J, Zhang KW, Shen Y, Huang ZJ, Li M, et al.

Identification of a high frequency transposon induced by tissue culture, nDaiZ, a member of the hAT family in rice

GENOMICS. 2009 MAR; 93 (3): 274-281

3422

7048 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

3423

7049 Ma XJ, Li-Ling J, Huang QL, Chen X, Hou L, et al.

Systematic analysis of alternative promoters correlated with alternative splicing in human genes

GENOMICS. 2009 MAY; 93 (5): 420-425

3424

7127 Marchani EE, Xing JC, Witherspoon DJ, Jorde LB, Rogers AR

Estimating the age of retrotransposon subfamilies using maximum likelihood

GENOMICS. 2009 JUL; 94 (1): 78-82

3425

7323 Cruickshanks HA, Tufarelli C

Isolation of cancer-specific chimeric transcripts induced by hypomethylation of the LINE-1 antisense promoter

GENOMICS. 2009 DEC; 94 (6): 397-406

3426

6223 Clark LA, Wahl JM, Rees CA, Strain GM, Cargill EJ, et al.

Canine SINEs and their effects on phenotypes of the domestic dog

GENOMICS OF DISEASE. 2008; : 79-87

3427

1077 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

3428

1752 Willer T, Amselgruber W, Deutzmann R, Strahl S

Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids

GLYCOBIOLOGY. 2002 NOV; 12 (11): 771-783

3429

2391 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

3430

807 Crocker PR, Zhang JQ

New I-type lectins of the CD33-related siglec subgroup identified through genomics

GLYCOGENOMICS: THE IMPACT OF GENOMICS AND INFORMATICS ON GLYCOBIOLOGY. 2002; (69): 83-94

Date / Author / Journal

LCS

GCS

LCR

3431

5591 Wigglesworth MJ, Wolfe LA, Wise A

Orphan seven transmembrane receptor screening

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

195

3432

6886 Gutierrez GR, de Roos B

Dietary fatty acids affecting hepatic metabolism and atherosclerosis - mechanisms unravelled using a proteomics approach

GRASAS Y ACEITES. 2009 JAN-MAR; 60 (1): 28-32

3433

4063 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

3434

2392 Thomas G, Cann H

Irruption of genomics in the search for disease related genes

GUT. 2003 MAY; 52: II1-II5

3435

664 Hallek M, Buening H, Ried M, Hacker U, Kurzeder C, et al.

Basics of gene therapy. Principles and development status

GYNAKOLOGE. 2001 DEC; 34 (12): 1182-+

3436

3061 Taylor RN

The future of endometriosis research: Genomics and proteomics?

GYNECOLOGIC AND OBSTETRIC INVESTIGATION. 2004; 57 (1): 47-49

3437

2069 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

3438

2644 DiSaia PJ, Bloss JD

Treatment of ovarian cancer: new strategies

GYNECOLOGIC ONCOLOGY. 2003 AUG; 90 (2): S24-S32

3439

6838 Oppelt P, Strick R, Strissel PL, Winzierl K, Beckmann MW, et al.

Expression of the human endogenous retroviruse-W envelope gene syncytin in endometriosis lesions

GYNECOLOGICAL ENDOCRINOLOGY. 2009; 25 (11): 741-747

3440

6462 Dierlamm J, Penas EMM, Bentink S, Wessendorf S, Berger H, et al.

Gain of chromosome region 18q21 including the MALT1 gene is associated with the activated B-cell-like gene expression subtype and increased BCL2 gene dosage and protein expression in diffuse large B-cell lymphoma

HAEMATOLOGICA-THE HEMATOLOGY JOURNAL. 2008 MAY; 93 (5): 688-696

Date / Author / Journal

LCS

GCS

LCR

3441

4484 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

3442

229 Sklar P

The genomic approach to candidate genes

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

3443

5025 Potash JB

Carving chaos: Genetics and the classification of mood and psychotic syndromes

HARVARD REVIEW OF PSYCHIATRY. 2006 MAR-APR; 14 (2): 47-63

152

3444

5026 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

3445

5027 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

3446

2560 Amundson SA, Fornace AJ

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

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

3447

289 Komajda M, Charron P

How will the human genome project change cardiovascular medicine?

HEART. 2001 AUG; 86 (2): 123-124

3448

1981 Christensen UB, Pedersen EB

Intercalating nucleic acids with pyrene nucleotide analogues as next-nearest neighbors for excimer fluorescence detection of single-point mutations under nonstringent hybridization conditions

HELVETICA CHIMICA ACTA. 2003; 86 (6): 2090-2097

3449

2239 Bataller R, North KE, Brenner DA

Genetic polymorphisms and the progression of liver fibrosis: A critical appraisal

HEPATOLOGY. 2003 MAR; 37 (3): 493-503

108

115

3450

2311 Thorgeirsson SS

Hunting for tumor suppressor genes in liver cancer

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

Date / Author / Journal

LCS

GCS

LCR

3451

5500 Juran BD, Lazaridis KN

Genomics and complex liver disease: Challenges and opportunities

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

3452

5788 Shin HJ, Anzai N, Enomoto A, He X, Kim DK, et al.

Novel liver-specific organic anion transporter OAT7 that operates the exchange of sulfate conjugates for short chain fatty acid butyrate

HEPATOLOGY. 2007 APR; 45 (4): 1046-1055

3453

2393 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

3454

5947 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

3455

2156 Hughes AL

Comparative genomics - Genomes of mice and men

HEREDITY. 2003 FEB; 90 (2): 115-116

3456

3452 Bofkin L, Whelan S

Functional needles in a genomic haystack

HEREDITY. 2004 MAY; 92 (5): 363-364

3457

5697 Leitch AR

Conserved gene order belies rapid genome turnover - The dynamic interplay between genomic DNA and the outside world

HEREDITY. 2007 FEB; 98 (2): 61-62

3458

7242 Sorek R

When new exons are born

HEREDITY. 2009 OCT; 103 (4): 279-280

3459

32 Prestegard JH

High resolution NMR of biomolecules

HIGH MAGNETIC FIELDS. 2001; 595: 426-434

3460

6839 Muotri AR, Zhao C, Marchetto MCN, Gage FH

Environmental Influence on L1 Retrotransposons in the Adult Hippocampus

HIPPOCAMPUS. 2009; 19 (10): 1002-1007

Date / Author / Journal

LCS

GCS

LCR

3461

1536 Roix J, Misteli T

Genomes, proteomes, and dynamic networks in the cell nucleus

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

3462

1153 Finta C, Warner SC, Zaphiropoulos PG

Intergenic mRNAs. Minor gene products or tools of diversity?

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

3463

4843 Kubicek S, Schotta G, Lachner M, Sengupta R, Kohlmaier A, et al.

The role of histone modifications in epigenetic transitions during normal and perturbed development

HISTONE CODE AND BEYOND: NEW APPROACHES TO CANCER THERAPY. 2006; 57: 1-27

3464

808 Chambers FM, Brain SA

Paradigm shifts in late-Holocene climatology?

HOLOCENE. 2002; 12 (2): 239-249

112

3465

1982 Curnoe D, Thorne A

Number of ancestral human species: a molecular perspective

HOMO-JOURNAL OF COMPARATIVE HUMAN BIOLOGY. 2003; 53 (3): 201-224

138

3466

1983 Polychronakos C

Impact of the human genome project on pediatric endocrinology

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

3467

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

Proteomic patterns of cultured breast cancer cells and epithelial mammary cells

3468

4844 Weber J, Futterer C, Gowri S, Attia R, Viovy JL

Towards a microfluidic chip for unknown mutation detection and genotyping

HOUILLE BLANCHE-REVUE INTERNATIONALE DE L EAU. 2006; (5): 40-44

3469

4845 Weber J, Futterer C, Gowri S, Attia R, Viovy JL

Towards a microfluidic chip for unknown mutation detection and genotyping

HOUILLE BLANCHE-REVUE INTERNATIONALE DE L EAU. 2006; (6): 40-44

3470

6840 Iimura T, Denans N, Pourquie O

ESTABLISHMENT OF HOX VERTEBRAL IDENTITIES IN THE EMBRYONIC SPINE PRECURSORS

HOX GENES. 2009; 88: 201-+

159

Date / Author / Journal

LCS

GCS

LCR

3471

6224 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

3472

1681 Stayner L, Toraason M, Hattis D

Risk assessment at the crossroads of the 21st century: Opportunities and challenges for research

HUMAN AND ECOLOGICAL RISK ASSESSMENT. 2002 OCT; 8 (6): 1195-1202

3473

3920 Devor EJ, Moffat-Wilson KA, Galbraith JJ

LOC 390443 (RNase 9) on chromosome 14q11.2 is related to the RNase a superfamily and contains a unique amino-terminal preproteinlike sequence

HUMAN BIOLOGY. 2004 DEC; 76 (6): 921-935

3474

4532 Mangeat B, Trono D

Lentiviral vectors and antiretroviral intrinsic immunity

HUMAN GENE THERAPY. 2005 AUG; 16 (8): 913-920

3475

290 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

3476

459 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

3477

665 Benjes SM, Morris CM

A full-length and potentially active LINE element is integrated polymorphically within the IGL locus in a genomically unstable region of chromosome 22

HUMAN GENETICS. 2001 DEC; 109 (6): 628-637

3478

666 Kelberman D, Tyson J, Chandler DC, McInerney AM, Slee J, et al.

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

HUMAN GENETICS. 2001 DEC; 109 (6): 638-645

3479

990 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

3480

1823 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

Date / Author / Journal

LCS

GCS

LCR

3481

2070 Knowles JW, Erickson LM, Guy VK, Sigel CS, Wilder JC, et al.

Common variations in noncoding regions of the human natriuretic peptide receptor A gene have quantitative effects

HUMAN GENETICS. 2003 JAN; 112 (1): 62-70

3482

2240 Sironi M, Pozzoli U, Cagliani R, Giorda R, Comi GP, et al.

Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot

HUMAN GENETICS. 2003 MAR; 112 (3): 272-288

3483

2394 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

3484

2561 Rothrock CR, Murgia A, Sartorato EL, Leonardi E, Wei SN, et al.

Connexin 26 35delG does not represent a mutational hotspot

HUMAN GENETICS. 2003 JUL; 113 (1): 18-23

3485

2562 Zhu LX, Swergold GD, Seldin MF

Examination of sequence homology between human chromosome 20 and the mouse genome: intense conservation of many genomic elements

HUMAN GENETICS. 2003 JUL; 113 (1): 60-70

3486

2645 van den Hurk JAJM, van de Pol DJR, Wissinger B, van Driel MA, Hoefsloot LH, et al.

Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon

HUMAN GENETICS. 2003 AUG; 113 (3): 268-275

3487

2848 Claverie-Martin F, Gonzalez-Acosta H, Flores C, Anton-Gamero M, Garcia-Nieto V

De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease

HUMAN GENETICS. 2003 NOV; 113 (6): 480-485

3488

3313 Timms KM, Wagner S, Samuels ME, Forbey K, Goldfine H, et al.

A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

HUMAN GENETICS. 2004 MAR; 114 (4): 349-353

3489

3453 Langan JE, Cole CG, Huckle EJ, Byrne S, McRonald FE, et al.

Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene

HUMAN GENETICS. 2004 MAY; 114 (6): 534-540

3490

3454 Winter J, Lehmann T, Krauss S, Trockenbacher A, Kijas Z, et al.

Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing

HUMAN GENETICS. 2004 MAY; 114 (6): 541-552

Date / Author / Journal

LCS

GCS

LCR

3491

3455 Hu FZ, Donfack J, Ahmed A, Dopico R, Johnson S, et al.

Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14

HUMAN GENETICS. 2004 MAY; 114 (6): 562-572

3492

4143 Shaw CJ, Lupski JR

Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms

HUMAN GENETICS. 2005 JAN; 116 (1-2): 1-7

3493

4579 Chen JM, Stenson PD, Cooper DN, Ferec C

A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease

HUMAN GENETICS. 2005 SEP; 117 (5): 411-427

133

3494

4635 Leimkuhler S, Charcosset M, Latour P, Dorche C, Kleppe S, et al.

Ten novel mutations in the molybdenum cofactor genes MOCS1 and MOCS2 and in vitro characterization of a MOCS2 mutation that abolishes the binding ability of molybdopterin synthase

HUMAN GENETICS. 2005 OCT; 117 (6): 565-570

3495

4636 Eagle ARR, Hanson RL, Jiang WP, Han XL, Matters GL, et al.

Meprin beta metalloprotease gene polymorphisms associated with diabetic nephropathy in the Pima Indians

HUMAN GENETICS. 2005 OCT; 118 (1): 12-22

3496

4918 Hassan MJ, Santos RLP, Rafiq MA, Chahrour MH, Pham TL, et al.

A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3

HUMAN GENETICS. 2006 JAN; 118 (5): 605-610

3497

5327 Santos RLP, Hassan MJ, Sikandar S, Lee K, Ali G, et al.

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2

HUMAN GENETICS. 2006 AUG; 120 (1): 85-92

3498

5836 Ali G, Chishti MS, Raza SI, John P, Ahmad W

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis

HUMAN GENETICS. 2007 MAY; 121 (3-4): 319-325

3499

6022 Jackson EM, Shaikh TH, Gururangan S, Jones MC, Malkin D, et al.

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor

HUMAN GENETICS. 2007 SEP; 122 (2): 117-127

3500

6326 Hassan MJ, Chishti MS, Jamal SM, Tariq M, Ahmad W

A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2

HUMAN GENETICS. 2008 FEB; 123 (1): 77-82

Initial sequencing and analysis of the human genome (Lander) The papers citing Lander ES, et al. "Initial sequencing and analysis of the human genome." NATURE. 2001 FEB 15; 409 (6822): 860-921	Historiographs	Glossary HistCite Guide About Grand Totals: LCS 38623, GCS 253809, CR 422506 Collection span: 2000 - 2010
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