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

Add FileX ?

Use wildcard '*' to add more than one file at a time. For example, if you have file1, file2, etc. all in the same folder or directory; first, locate one of the files with the [Browse...] button. Then alter the file path in the box above to include '*' character (eg. file*). Wildcard '?' to blanket only one character works too.
Note: In Windows you can select multiple files and "drag and drop" them onto HistCite icon or shortcut. The program would start and load those files.

#	Date / Author / Journal	LCS	GCS	LCR	CR
101	733 Saito H, Nakajima T, Ahn KM Mast cell transcriptome project for discovering new regulatory molecules ALLERGY: AN EXPANDING CHALLENGE IN THE 21ST CENTURY. 2002; : 33-38	0	0	7	17
102	5551 Park JW, Graveley BR Complex alternative splicing ALTERNATIVE SPLICING IN THE POSTGENOMIC ERA. 2007; 623: 50-63	0	3	7	51
103	5552 Lareau LF, Brooks AN, Soergel DAW, Meng Q, Brenner SE The coupling of alternative splicing and nonsense-mediated mRNA decay ALTERNATIVE SPLICING IN THE POSTGENOMIC ERA. 2007; 623: 190-211	2	13	15	109
104	4620 Soto JG Understanding the human genome project: Using stations to provide a comprehensive overview AMERICAN BIOLOGY TEACHER. 2005 OCT; 67 (8): 475-484	0	1	2	10
105	4967 Bhattacharjee JK, Janssen GR, Gregg TG Human genealogy: How wide & deep do our genetic connections go? AMERICAN BIOLOGY TEACHER. 2006 FEB; 68 (2): 69-71	0	0	3	13
106	5081 Gregg T, Janssen G, Bhattacharjee J On "human genealogy" - Response AMERICAN BIOLOGY TEACHER. 2006 APR; 68 (4): 198-198	0	0	1	3
107	5728 Kass DH Simple & rapid generation of complex DNA profiles for the undergraduate laboratory AMERICAN BIOLOGY TEACHER. 2007 MAR; 69 (3): 163-168	1	2	4	11
108	1730 Agema WRP, Jukema JW, Zwinderman AH, van der Wall EE A meta-analysis of the angiotensin-converting enzyme gene polymorphism and restenosis after percutaneous transluminal coronary revascularization: Evidence for publication bias AMERICAN HEART JOURNAL. 2002 NOV; 144 (5): 760-768	1	22	2	50
109	6547 Weisberg MB 50 years of hypnosis in medicine and clinical health psychology: A synthesis of cultural crosscurrents AMERICAN JOURNAL OF CLINICAL HYPNOSIS. 2008 JUL; 51 (1): 13-27	0	0	1	71
110	1175 Austin MA Ethical issues in human genome epidemiology: A case study based on the Japanese American family study in Seattle, Washington AMERICAN JOURNAL OF EPIDEMIOLOGY. 2002 APR 1; 155 (7): 585-592	1	14	4	59
#	Date / Author / Journal	LCS	GCS	LCR	CR
111	1552 Ioannidis JPA, Rosenberg PS, Goedert JJ, O'Brien TR, Int Meta-Anal HIV Host Genetics Commentary: Meta-analysis of individual participants' data in genetic epidemiology AMERICAN JOURNAL OF EPIDEMIOLOGY. 2002 AUG 1; 156 (3): 204-210	1	49	1	48
112	2271 McCanlies EC, Kreiss K, Andrew M, Weston A HLA-DPB1 and chronic beryllium disease: A HuGE review AMERICAN JOURNAL OF EPIDEMIOLOGY. 2003 MAR 1; 157 (5): 388-398	0	30	1	79
113	5245 Burchard EG Importance of race/ethnicity and genetics in biomedical research and clinical practice: Lessons learned from the genetics of asthma in Latino Americans (GALA) study. AMERICAN JOURNAL OF EPIDEMIOLOGY. 2006 JUN 1; 163 (11): S84-S84	0	0	2	3
114	6784 Sagoo GS, Tatt I, Salanti G, Butterworth AS, Sarwar N, et al. Seven Lipoprotein Lipase Gene Polymorphisms, Lipid Fractions, and Coronary Disease: A HuGE Association Review and Meta-Analysis AMERICAN JOURNAL OF EPIDEMIOLOGY. 2008 DEC 1; 168 (11): 1233-1246	0	3	2	151
115	6906 Chang MH, Lindegren ML, Butler MA, Chanock SJ, Dowling NF, et al. Prevalence in the United States of Selected Candidate Gene Variants AMERICAN JOURNAL OF EPIDEMIOLOGY. 2009 JAN 1; 169 (1): 54-66	0	5	7	76
116	2834 McGinnis JM A vision for health in our new century AMERICAN JOURNAL OF HEALTH PROMOTION. 2003 NOV-DEC; 18 (2): 146-150	0	2	1	28
117	1189 Brock TP, Faulkner CM, Williams DM, Smith SR Continuing-education programs in pharmacogenomics for pharmacists AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2002 APR 15; 59 (8): 722-725	2	8	1	14
118	1636 Hayney MS Pharmacogenomics and infectious diseases: Impact on drug response and applications to disease management AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2002 SEP 1; 59 (17): 1626-1631	1	4	2	36
119	4224 Kreiner T, Buck KT Moving toward whole-genome analysis: A technology perspective AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2005 FEB 1; 62 (3): 296-305	0	3	6	84
120	7154 Sebastiani P, Timofeev N, Dworkis DA, Perls TT, Steinberg MH Genome-wide association studies and the genetic dissection of complex traits AMERICAN JOURNAL OF HEMATOLOGY. 2009 AUG; 84 (8): 504-515	0	1	4	144
#	Date / Author / Journal	LCS	GCS	LCR	CR
121	2697 Vandenbergh DJ, Anthony K, Whitfield KE Optimizing DNA yield from buccal swabs in the elderly: Attempts to promote buccal cell growth in culture AMERICAN JOURNAL OF HUMAN BIOLOGY. 2003 SEP-OCT; 15 (5): 637-642	0	5	2	22
122	3432 Cotrim NH, Auricchio MTBM, Vicente JP, Otto PA, Mingroni-Netto RC Polymorphic Alu insertions in six Brazilian African-derived populations AMERICAN JOURNAL OF HUMAN BIOLOGY. 2004 MAY-JUN; 16 (3): 264-277	5	8	2	51
123	4120 Worthman CM, Kuzara J Life history and the early origins of health differentials AMERICAN JOURNAL OF HUMAN BIOLOGY. 2005 JAN-FEB; 17 (1): 95-112	0	29	3	145
124	171 Giannelli F Mitochondria and the quality of human gametes AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUN; 68 (6): 1535-1537	0	4	1	7
125	210 Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, et al. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUL; 69 (1): 25-34	1	135	1	52
126	211 Rannala B, Reeve JP High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUL; 69 (1): 159-178	5	57	2	36
127	272 Krawczak M, Cooper DN, Schmidtke J Estimating the efficacy and efficiency of cascade genetic screening AMERICAN JOURNAL OF HUMAN GENETICS. 2001 AUG; 69 (2): 361-370	1	25	2	28
128	347 Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, et al. Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 516-527	6	49	2	38
129	348 Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, et al. A genomewide scan for loci predisposing to type 2 diabetes in a UK population (the Diabetes UK Warren 2 repository): Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 553-569	9	189	1	70
130	349 Ardlie K, Liu-Cordero SN, Eberle MA, Daly M, Barrett J, et al. Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 582-589	4	69	1	40
#	Date / Author / Journal	LCS	GCS	LCR	CR
131	429 Atkinson TP, Schaffer AA, Grimbacher B, Schroeder HW, Woellner C, et al. An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family AMERICAN JOURNAL OF HUMAN GENETICS. 2001 OCT; 69 (4): 791-803	0	19	2	66
132	531 Lefevre C, Jobard F, Caux F, Bouadjar B, Karaduman A, et al. Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome AMERICAN JOURNAL OF HUMAN GENETICS. 2001 NOV; 69 (5): 1002-1012	0	119	1	37
133	860 Bailey JA, Yavor AM, Viggiano L, Misceo D, Horvath JE, et al. Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22 AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JAN; 70 (1): 83-100	51	109	6	61
134	861 DeWan AT, Parrado AR, Matise TC, Leal SM The map problem: A comparison of genetic and sequence-based physical maps AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JAN; 70 (1): 101-107	3	10	5	23
135	955 Willard HF On black boxes and storytellers: Lessons learned in human genetics AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 285-296	1	2	3	23
136	956 Schaid DJ, Rowland CM, Tines DE, Jacobson RM, Poland GA Score tests for association between traits and haplotypes when linkage phase is ambiguous AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 425-434	11	903	2	40
137	957 Wiltshire S, Frayling TM, Hattersley AT, Hitman GA, Walker M, et al. Evidence for linkage of stature to chromosome 3p26 in a large UK family data set ascertained for type 2 diabetes AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 543-546	0	41	2	18
138	958 Goodman FR, Majewski F, Collins AL, Scambler PJ A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 547-555	1	40	2	37
139	1053 Gretarsdottir S, Sveinbjornsdottir S, Jonsson HH, Jakobsson F, Einarsdottir E, et al. Localization of a susceptibility gene for common forms of stroke to 5q12 AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAR; 70 (3): 593-603	4	114	2	44
140	1054 Frosk P, Weiler T, Nylen E, Sudha T, Greenberg CR, et al. Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAR; 70 (3): 663-672	0	66	2	33
#	Date / Author / Journal	LCS	GCS	LCR	CR
141	1211 Howe JR, Shellnut J, Wagner B, Ringold JC, Sayed MG, et al. Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAY; 70 (5): 1357-1362	0	15	2	28
142	1212 Hobbs MR, Rosen IB, Jackson CE Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2 AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAY; 70 (5): 1376-1377	0	3	1	6
143	1318 Matise TC, Porter CJ, Buyske S, Cuttichia AJ, Sulman EP, et al. Systematic evaluation of map quality: Human chromosome 22 AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUN; 70 (6): 1398-1410	3	13	5	29
144	1319 Stone S, Abkevich V, Hunt SC, Gutin A, Russell DL, et al. A major predisposition locus for severe obesity, at 4p15-p14 AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUN; 70 (6): 1459-1468	2	71	2	50
145	1419 Wang LL, Worley K, Gannavarapu A, Chintagumpala MM, Levy ML, et al. Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUL; 71 (1): 165-167	0	27	1	13
146	1511 Myers JS, Vincent BJ, Udall H, Watkins WS, Morrish TA, et al. A comprehensive analysis of recently integrated human Ta L1 elements AMERICAN JOURNAL OF HUMAN GENETICS. 2002 AUG; 71 (2): 312-326	53	67	9	70
147	1512 Brouha B, Meischl C, Ostertag E, de Boer M, Zhang Y, et al. Evidence consistent with human L1 retrotransposition in maternal meiosis I AMERICAN JOURNAL OF HUMAN GENETICS. 2002 AUG; 71 (2): 327-336	25	32	3	40
148	1663 Weber JL, David D, Heil J, Fan Y, Zhao CF, et al. Human diallelic insertion/deletion polymorphisms AMERICAN JOURNAL OF HUMAN GENETICS. 2002 OCT; 71 (4): 854-862	10	67	1	27
149	2220 Mathews LM, Chi SY, Greenberg N, Ovchinnikov I, Swergold GD Large differences between LINE-1 amplification rates in the human and chimpanzee lineages AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAR; 72 (3): 739-748	8	11	7	43
150	2291 Badge RM, Alisch RS, Moran JV ATLAS: A system to selectively identify human-specific L1 insertions AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 823-838	23	30	6	46
#	Date / Author / Journal	LCS	GCS	LCR	CR
151	2292 Pajukanta P, Allayee H, Krass KL, Kuraishy A, Soro A, et al. Combined analysis of genome scans of Dutch and Finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 903-917	0	52	6	69
152	2293 Flanigan KM, von Niederhausern A, Dunn DM, Alder J, Mendell JR, et al. Rapid direct sequence analysis of the dystrophin gene AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 931-939	2	61	1	18
153	2372 Stankiewicz P, Shaw CJ, Dapper JD, Wakui K, Shaffer LG, et al. Genome architecture catalyzes nonrecurrent chromosomal rearrangements AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAY; 72 (5): 1101-1116	12	90	14	66
154	2373 Zhao LP, Li SYS, Khalid N A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAY; 72 (5): 1231-1250	4	107	4	43
155	2617 Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set AMERICAN JOURNAL OF HUMAN GENETICS. 2003 AUG; 73 (2): 271-284	4	71	3	46
156	2767 Bailey JA, Liu G, Eichler EE An Alu transposition model for the origin and expansion of human segmental duplications AMERICAN JOURNAL OF HUMAN GENETICS. 2003 OCT; 73 (4): 823-834	75	159	11	37
157	2903 Lutz SM, Vincent BJ, Kazazian HH, Balzer MA, Moran JV Allelic heterogeneity in LINE-1 retrotransposition activity AMERICAN JOURNAL OF HUMAN GENETICS. 2003 DEC; 73 (6): 1431-1437	17	19	7	38
158	2904 Ostertag EM, Goodier JL, Zhang Y, Kazazian HH SVA elements are nonautonomous retrotransposons that cause disease in humans AMERICAN JOURNAL OF HUMAN GENETICS. 2003 DEC; 73 (6): 1444-1451	44	55	11	40
159	3131 Barbouti A, Stankiewicz P, Nusbaum C, Cuomo C, Cook A, et al. The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JAN; 74 (1): 1-10	7	40	10	39
160	3132 Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, et al. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JAN; 74 (1): 106-120	17	643	3	41
#	Date / Author / Journal	LCS	GCS	LCR	CR
161	3225 Wen G, Mahata SK, Cadman P, Mahata M, Ghosh S, et al. Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology AMERICAN JOURNAL OF HUMAN GENETICS. 2004 FEB; 74 (2): 197-207	2	35	2	56
162	3297 Valle D 2003 ASHG Presidential Address - Genetics, individuality, and medicine in the 21st century AMERICAN JOURNAL OF HUMAN GENETICS. 2004 MAR; 74 (3): 374-381	0	11	10	74
163	3433 Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, et al. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus AMERICAN JOURNAL OF HUMAN GENETICS. 2004 MAY; 74 (5): 931-944	0	84	8	59
164	3587 Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, et al. Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JUL; 75 (1): 35-43	0	94	3	20
165	3716 Chiang AP, Nishimura D, Searby C, Elbedour K, Carmi R, et al. Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3) AMERICAN JOURNAL OF HUMAN GENETICS. 2004 SEP; 75 (3): 475-484	1	72	3	36
166	4621 Berg K, Bonham V, Boyer J, Brody L, Brooks L, et al. The use of racial, ethnic, and ancestral categories in human genetics research AMERICAN JOURNAL OF HUMAN GENETICS. 2005 OCT; 77 (4): 519-532	0	21	9	205
167	5082 Pe'er I, Chretien YR, de Bakker PIW, Barrett JC, Daly MJ, et al. Biases and reconciliation in estimates of linkage disequilibrium in the human genome AMERICAN JOURNAL OF HUMAN GENETICS. 2006 APR; 78 (4): 588-603	3	21	7	43
168	5083 Mills RE, Bennett EA, Iskow RC, Luttig CT, Tsui C, et al. Recently mobilized Transposons in the human and chimpanzee Genomes AMERICAN JOURNAL OF HUMAN GENETICS. 2006 APR; 78 (4): 671-679	21	26	12	28
169	5272 Sen SK, Han KD, Wang JX, Lee J, Wang H, et al. Human genomic deletions mediated by recombination between Alu elements AMERICAN JOURNAL OF HUMAN GENETICS. 2006 JUL; 79 (1): 41-53	30	59	22	60
170	5273 Flanagan JM, Popendikyte V, Pozdniakovaite N, Sobolev M, Assadzadeh A, et al. Intra-and interindividual epigenetic variation in human germ cells AMERICAN JOURNAL OF HUMAN GENETICS. 2006 JUL; 79 (1): 67-84	3	41	8	71
#	Date / Author / Journal	LCS	GCS	LCR	CR
171	6149 Stokowski RP, Pant PVK, Dadd T, Fereday A, Hinds DA, et al. A genomewide association study of skin pigmentation in a South Asian population AMERICAN JOURNAL OF HUMAN GENETICS. 2007 DEC; 81 (6): 1119-1132	2	23	3	55
172	6316 van Zelm MC, Geertsema C, Nieuwenhuis N, de Ridder D, Conley ME, et al. Gross deletions involving IGHM, BTK, or Artemis: A model for genomic lesions mediated by transposable elements AMERICAN JOURNAL OF HUMAN GENETICS. 2008 FEB; 82 (2): 320-332	1	9	4	66
173	6317 Baldwin EL, May LE, Justice AN, Martin CL, Ledbetter DH Mechanisms and consequences of small supernumerary marker chromosomes: From Barbara McClintock to modern genetic-counseling issues AMERICAN JOURNAL OF HUMAN GENETICS. 2008 FEB; 82 (2): 398-410	1	9	10	66
174	7025 Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, et al. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources AMERICAN JOURNAL OF HUMAN GENETICS. 2009 APR 10; 84 (4): 524-533	0	4	3	42
175	430 Greendale K, Pyeritz RE Empowering primary care health professionals in medical genetics: How soon? How fast? How far? AMERICAN JOURNAL OF MEDICAL GENETICS. 2001 FAL; 106 (3): 223-232	0	50	4	47
176	1313 Pociot F, Karlsen AE Combined genome and proteome approach to identify new susceptibility genes AMERICAN JOURNAL OF MEDICAL GENETICS. 2002 MAY 30; 115 (1): 55-60	2	12	1	27
177	1705 Goodman FR Limb malformations and the human HOX genes AMERICAN JOURNAL OF MEDICAL GENETICS. 2002 OCT 15; 112 (3): 256-265	0	65	3	90
178	2356 McCormack WM, Shen JJ, Curry SM, Berend SA, Kashork C, et al. Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation (vol 112, pg 384, 2002) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 APR 15; 118A (2): 200-+	0	0	1	19
179	2433 de Pater JM, Smeets DFCM, Scheres JMJC Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved? AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 MAY 15; 119A (1): 26-31	0	5	1	37
180	2599 Bannykh SI, Emery SC, Gerber JK, Jones KL, Benirschke K, et al. Aberrant Pax1 and Pax9 expression in Jarcho-Levin syndrome: Report of two Caucasian siblings and literature review AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 JUL 15; 120A (2): 241-246	0	11	1	40
#	Date / Author / Journal	LCS	GCS	LCR	CR
181	2948 Irving M, Hanson H, Turnpenny P, Brewer C, Ogilvie CM, et al. Deletion of the distal long arm of chromosome 10; Is there a characteristic phenotype? A report of 15 de novo and familial cases AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 DEC 1; 123A (2): 153-163	0	15	1	24
182	4235 Aslam M, Wajid M, Chahrour MH, Ansar M, Haque S, et al. A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 FEB 15; 133A (1): 18-22	0	2	2	23
183	4236 Mir A, Ansar M, Chahrour MH, Phain TL, Wajid M, et al. Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31 AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 FEB 15; 133A (1): 23-26	0	1	2	17
184	4285 Amor DJ, Voullaire L, Bentley K, Savarirayan R, Amor DJ Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 MAR 1; 133A (2): 151-157	0	5	2	47
185	4363 Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, et al. Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: Is less more? AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 APR 30; 134A (3): 259-267	0	87	4	30
186	4559 Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, et al. A report of three patients with an interstitial deletion of chromosome 15q24 AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 AUG 15; 137A (1): 65-71	0	11	2	29
187	5008 Zhang LL, Wang T, Wright AF, Suri M, Schwartz CE, et al. A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindred AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2006 FEB 15; 140A (4): 349-357	0	4	1	33
188	5766 Barber JCK, Maloney VK, Kirchhoff M, Thomas NS, Boyle TA, et al. Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 MAR 15; 143A (6): 615-618	0	1	1	10
189	5805 Feldman GJ, Billings PC, Patel RV, Caron RJ, Guenther C, et al. Over-expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: A new syndrome AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 APR 1; 143A (7): 699-706	0	4	1	27
190	5922 Probst FJ, Roeder ER, Enciso VB, Ou ZS, Cooper ML, et al. Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 JUN 15; 143A (12): 1358-1365	0	15	3	41
#	Date / Author / Journal	LCS	GCS	LCR	CR
191	6658 Jones JR, Skinner C, Friez MJ, Schwartz CE, Stevenson RE Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2008 SEP 1; 146A (17): 2213-2220	0	2	1	104
192	6708 Kulikowski LD, Bellucco FTS, Nogueira SI, Christofolini DM, Smith MDC, et al. Pure Duplication 1q41-qter: Further Delineation of Trisomy 1q Syndromes AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2008 OCT 15; 146A (20): 2663-2667	0	1	1	16
193	6919 Misceo D, Rocchi M, van der Hagen CB, Frengen E A Partial Trisomy 1q Patient With a Deletion 1q22 and an Insertion 1(q42q44) Into 1q22 AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2009 FEB; 149A (2): 290-293	0	0	1	14
194	6704 Neale BM, Purcell S The Positives, Protocols, and Perils of Genome-Wide Association AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2008 OCT 5; 147B (7): 1288-1294	0	6	2	78
195	2682 Platte P, Papanicolaou GJ, Johnston J, Klein CM, Doheny KF, et al. A study of linkage and association of body mass index in the Old Order Amish AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2003 AUG 15; 121C (1): 71-80	0	29	2	64
196	2886 Schulze TG, McMahon FJ Genetic linkage and association studies in bipolar affective disorder: A time for optimism AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2003 NOV 15; 123C (1): 36-47	0	22	11	115
197	7071 Haque FN, Gottesman II, Wong AHC Not Really Identical: Epigenetic Differences in Monozygotic Twins and Implications for Twin Studies in Psychiatry AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2009 MAY 15; 151C (2): 136-141	0	2	2	56
198	2357 Crowley WF Translation of basic research into useful treatments: How often does it occur? AMERICAN JOURNAL OF MEDICINE. 2003 APR 15; 114 (6): 503-505	0	13	2	13
199	5686 Pennell CE, Jacobsson B, Williams SM, Buns RM, Muglia LJ, et al. Genetic epidemiologic studies of preterm birth: guidelines for research AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY. 2007 FEB; 196 (2): 107-118	0	14	2	133
200	2294 Moroi SE, Gokhale PA, Schteingart MT, Sugar A, Downs CA, et al. Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy AMERICAN JOURNAL OF OPHTHALMOLOGY. 2003 APR; 135 (4): 461-470	0	11	1	42

Date / Author / Journal

LCS

GCS

LCR

101

733 Saito H, Nakajima T, Ahn KM

Mast cell transcriptome project for discovering new regulatory molecules

ALLERGY: AN EXPANDING CHALLENGE IN THE 21ST CENTURY. 2002; : 33-38

102

5551 Park JW, Graveley BR

Complex alternative splicing

ALTERNATIVE SPLICING IN THE POSTGENOMIC ERA. 2007; 623: 50-63

103

5552 Lareau LF, Brooks AN, Soergel DAW, Meng Q, Brenner SE

The coupling of alternative splicing and nonsense-mediated mRNA decay

ALTERNATIVE SPLICING IN THE POSTGENOMIC ERA. 2007; 623: 190-211

109

104

4620 Soto JG

Understanding the human genome project: Using stations to provide a comprehensive overview

AMERICAN BIOLOGY TEACHER. 2005 OCT; 67 (8): 475-484

105

4967 Bhattacharjee JK, Janssen GR, Gregg TG

Human genealogy: How wide & deep do our genetic connections go?

AMERICAN BIOLOGY TEACHER. 2006 FEB; 68 (2): 69-71

106

5081 Gregg T, Janssen G, Bhattacharjee J

On "human genealogy" - Response

AMERICAN BIOLOGY TEACHER. 2006 APR; 68 (4): 198-198

107

5728 Kass DH

Simple & rapid generation of complex DNA profiles for the undergraduate laboratory

AMERICAN BIOLOGY TEACHER. 2007 MAR; 69 (3): 163-168

108

1730 Agema WRP, Jukema JW, Zwinderman AH, van der Wall EE

A meta-analysis of the angiotensin-converting enzyme gene polymorphism and restenosis after percutaneous transluminal coronary revascularization: Evidence for publication bias

AMERICAN HEART JOURNAL. 2002 NOV; 144 (5): 760-768

109

6547 Weisberg MB

50 years of hypnosis in medicine and clinical health psychology: A synthesis of cultural crosscurrents

AMERICAN JOURNAL OF CLINICAL HYPNOSIS. 2008 JUL; 51 (1): 13-27

110

1175 Austin MA

Ethical issues in human genome epidemiology: A case study based on the Japanese American family study in Seattle, Washington

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2002 APR 1; 155 (7): 585-592

Date / Author / Journal

LCS

GCS

LCR

111

1552 Ioannidis JPA, Rosenberg PS, Goedert JJ, O'Brien TR, Int Meta-Anal HIV Host Genetics

Commentary: Meta-analysis of individual participants' data in genetic epidemiology

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2002 AUG 1; 156 (3): 204-210

112

2271 McCanlies EC, Kreiss K, Andrew M, Weston A

HLA-DPB1 and chronic beryllium disease: A HuGE review

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2003 MAR 1; 157 (5): 388-398

113

5245 Burchard EG

Importance of race/ethnicity and genetics in biomedical research and clinical practice: Lessons learned from the genetics of asthma in Latino Americans (GALA) study.

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2006 JUN 1; 163 (11): S84-S84

114

6784 Sagoo GS, Tatt I, Salanti G, Butterworth AS, Sarwar N, et al.

Seven Lipoprotein Lipase Gene Polymorphisms, Lipid Fractions, and Coronary Disease: A HuGE Association Review and Meta-Analysis

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2008 DEC 1; 168 (11): 1233-1246

151

115

6906 Chang MH, Lindegren ML, Butler MA, Chanock SJ, Dowling NF, et al.

Prevalence in the United States of Selected Candidate Gene Variants

AMERICAN JOURNAL OF EPIDEMIOLOGY. 2009 JAN 1; 169 (1): 54-66

116

2834 McGinnis JM

A vision for health in our new century

AMERICAN JOURNAL OF HEALTH PROMOTION. 2003 NOV-DEC; 18 (2): 146-150

117

1189 Brock TP, Faulkner CM, Williams DM, Smith SR

Continuing-education programs in pharmacogenomics for pharmacists

AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2002 APR 15; 59 (8): 722-725

118

1636 Hayney MS

Pharmacogenomics and infectious diseases: Impact on drug response and applications to disease management

AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2002 SEP 1; 59 (17): 1626-1631

119

4224 Kreiner T, Buck KT

Moving toward whole-genome analysis: A technology perspective

AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY. 2005 FEB 1; 62 (3): 296-305

120

7154 Sebastiani P, Timofeev N, Dworkis DA, Perls TT, Steinberg MH

Genome-wide association studies and the genetic dissection of complex traits

AMERICAN JOURNAL OF HEMATOLOGY. 2009 AUG; 84 (8): 504-515

144

Date / Author / Journal

LCS

GCS

LCR

121

2697 Vandenbergh DJ, Anthony K, Whitfield KE

Optimizing DNA yield from buccal swabs in the elderly: Attempts to promote buccal cell growth in culture

AMERICAN JOURNAL OF HUMAN BIOLOGY. 2003 SEP-OCT; 15 (5): 637-642

122

3432 Cotrim NH, Auricchio MTBM, Vicente JP, Otto PA, Mingroni-Netto RC

Polymorphic Alu insertions in six Brazilian African-derived populations

AMERICAN JOURNAL OF HUMAN BIOLOGY. 2004 MAY-JUN; 16 (3): 264-277

123

4120 Worthman CM, Kuzara J

Life history and the early origins of health differentials

AMERICAN JOURNAL OF HUMAN BIOLOGY. 2005 JAN-FEB; 17 (1): 95-112

145

124

171 Giannelli F

Mitochondria and the quality of human gametes

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUN; 68 (6): 1535-1537

125

210 Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, et al.

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUL; 69 (1): 25-34

135

126

211 Rannala B, Reeve JP

High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 JUL; 69 (1): 159-178

127

272 Krawczak M, Cooper DN, Schmidtke J

Estimating the efficacy and efficiency of cascade genetic screening

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 AUG; 69 (2): 361-370

128

347 Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, et al.

Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 516-527

129

348 Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, et al.

A genomewide scan for loci predisposing to type 2 diabetes in a UK population (the Diabetes UK Warren 2 repository): Analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 553-569

189

130

349 Ardlie K, Liu-Cordero SN, Eberle MA, Daly M, Barrett J, et al.

Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 SEP; 69 (3): 582-589

Date / Author / Journal

LCS

GCS

LCR

131

429 Atkinson TP, Schaffer AA, Grimbacher B, Schroeder HW, Woellner C, et al.

An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 OCT; 69 (4): 791-803

132

531 Lefevre C, Jobard F, Caux F, Bouadjar B, Karaduman A, et al.

Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome

AMERICAN JOURNAL OF HUMAN GENETICS. 2001 NOV; 69 (5): 1002-1012

119

133

860 Bailey JA, Yavor AM, Viggiano L, Misceo D, Horvath JE, et al.

Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JAN; 70 (1): 83-100

109

134

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

The map problem: A comparison of genetic and sequence-based physical maps

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JAN; 70 (1): 101-107

135

955 Willard HF

On black boxes and storytellers: Lessons learned in human genetics

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 285-296

136

956 Schaid DJ, Rowland CM, Tines DE, Jacobson RM, Poland GA

Score tests for association between traits and haplotypes when linkage phase is ambiguous

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 425-434

903

137

957 Wiltshire S, Frayling TM, Hattersley AT, Hitman GA, Walker M, et al.

Evidence for linkage of stature to chromosome 3p26 in a large UK family data set ascertained for type 2 diabetes

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 543-546

138

958 Goodman FR, Majewski F, Collins AL, Scambler PJ

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 FEB; 70 (2): 547-555

139

1053 Gretarsdottir S, Sveinbjornsdottir S, Jonsson HH, Jakobsson F, Einarsdottir E, et al.

Localization of a susceptibility gene for common forms of stroke to 5q12

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAR; 70 (3): 593-603

114

140

1054 Frosk P, Weiler T, Nylen E, Sudha T, Greenberg CR, et al.

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAR; 70 (3): 663-672

Date / Author / Journal

LCS

GCS

LCR

141

1211 Howe JR, Shellnut J, Wagner B, Ringold JC, Sayed MG, et al.

Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAY; 70 (5): 1357-1362

142

1212 Hobbs MR, Rosen IB, Jackson CE

Revised 14.7-cM locus for the hyperparathyroidism-jaw tumor syndrome gene, HRPT2

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 MAY; 70 (5): 1376-1377

143

1318 Matise TC, Porter CJ, Buyske S, Cuttichia AJ, Sulman EP, et al.

Systematic evaluation of map quality: Human chromosome 22

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUN; 70 (6): 1398-1410

144

1319 Stone S, Abkevich V, Hunt SC, Gutin A, Russell DL, et al.

A major predisposition locus for severe obesity, at 4p15-p14

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUN; 70 (6): 1459-1468

145

1419 Wang LL, Worley K, Gannavarapu A, Chintagumpala MM, Levy ML, et al.

Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 JUL; 71 (1): 165-167

146

1511 Myers JS, Vincent BJ, Udall H, Watkins WS, Morrish TA, et al.

A comprehensive analysis of recently integrated human Ta L1 elements

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 AUG; 71 (2): 312-326

147

1512 Brouha B, Meischl C, Ostertag E, de Boer M, Zhang Y, et al.

Evidence consistent with human L1 retrotransposition in maternal meiosis I

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 AUG; 71 (2): 327-336

148

1663 Weber JL, David D, Heil J, Fan Y, Zhao CF, et al.

Human diallelic insertion/deletion polymorphisms

AMERICAN JOURNAL OF HUMAN GENETICS. 2002 OCT; 71 (4): 854-862

149

2220 Mathews LM, Chi SY, Greenberg N, Ovchinnikov I, Swergold GD

Large differences between LINE-1 amplification rates in the human and chimpanzee lineages

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAR; 72 (3): 739-748

150

2291 Badge RM, Alisch RS, Moran JV

ATLAS: A system to selectively identify human-specific L1 insertions

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 823-838

Date / Author / Journal

LCS

GCS

LCR

151

2292 Pajukanta P, Allayee H, Krass KL, Kuraishy A, Soro A, et al.

Combined analysis of genome scans of Dutch and Finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 903-917

152

2293 Flanigan KM, von Niederhausern A, Dunn DM, Alder J, Mendell JR, et al.

Rapid direct sequence analysis of the dystrophin gene

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 APR; 72 (4): 931-939

153

2372 Stankiewicz P, Shaw CJ, Dapper JD, Wakui K, Shaffer LG, et al.

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAY; 72 (5): 1101-1116

154

2373 Zhao LP, Li SYS, Khalid N

A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 MAY; 72 (5): 1231-1250

107

155

2617 Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, et al.

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 AUG; 73 (2): 271-284

156

2767 Bailey JA, Liu G, Eichler EE

An Alu transposition model for the origin and expansion of human segmental duplications

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 OCT; 73 (4): 823-834

159

157

2903 Lutz SM, Vincent BJ, Kazazian HH, Balzer MA, Moran JV

Allelic heterogeneity in LINE-1 retrotransposition activity

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 DEC; 73 (6): 1431-1437

158

2904 Ostertag EM, Goodier JL, Zhang Y, Kazazian HH

SVA elements are nonautonomous retrotransposons that cause disease in humans

AMERICAN JOURNAL OF HUMAN GENETICS. 2003 DEC; 73 (6): 1444-1451

159

3131 Barbouti A, Stankiewicz P, Nusbaum C, Cuomo C, Cook A, et al.

The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JAN; 74 (1): 1-10

160

3132 Carlson CS, Eberle MA, Rieder MJ, Yi Q, Kruglyak L, et al.

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JAN; 74 (1): 106-120

643

Date / Author / Journal

LCS

GCS

LCR

161

3225 Wen G, Mahata SK, Cadman P, Mahata M, Ghosh S, et al.

Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 FEB; 74 (2): 197-207

162

3297 Valle D

2003 ASHG Presidential Address - Genetics, individuality, and medicine in the 21st century

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 MAR; 74 (3): 374-381

163

3433 Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, et al.

The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 MAY; 74 (5): 931-944

164

3587 Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, et al.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 JUL; 75 (1): 35-43

165

3716 Chiang AP, Nishimura D, Searby C, Elbedour K, Carmi R, et al.

Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

AMERICAN JOURNAL OF HUMAN GENETICS. 2004 SEP; 75 (3): 475-484

166

4621 Berg K, Bonham V, Boyer J, Brody L, Brooks L, et al.

The use of racial, ethnic, and ancestral categories in human genetics research

AMERICAN JOURNAL OF HUMAN GENETICS. 2005 OCT; 77 (4): 519-532

205

167

5082 Pe'er I, Chretien YR, de Bakker PIW, Barrett JC, Daly MJ, et al.

Biases and reconciliation in estimates of linkage disequilibrium in the human genome

AMERICAN JOURNAL OF HUMAN GENETICS. 2006 APR; 78 (4): 588-603

168

5083 Mills RE, Bennett EA, Iskow RC, Luttig CT, Tsui C, et al.

Recently mobilized Transposons in the human and chimpanzee Genomes

AMERICAN JOURNAL OF HUMAN GENETICS. 2006 APR; 78 (4): 671-679

169

5272 Sen SK, Han KD, Wang JX, Lee J, Wang H, et al.

Human genomic deletions mediated by recombination between Alu elements

AMERICAN JOURNAL OF HUMAN GENETICS. 2006 JUL; 79 (1): 41-53

170

5273 Flanagan JM, Popendikyte V, Pozdniakovaite N, Sobolev M, Assadzadeh A, et al.

Intra-and interindividual epigenetic variation in human germ cells

AMERICAN JOURNAL OF HUMAN GENETICS. 2006 JUL; 79 (1): 67-84

Date / Author / Journal

LCS

GCS

LCR

171

6149 Stokowski RP, Pant PVK, Dadd T, Fereday A, Hinds DA, et al.

A genomewide association study of skin pigmentation in a South Asian population

AMERICAN JOURNAL OF HUMAN GENETICS. 2007 DEC; 81 (6): 1119-1132

172

6316 van Zelm MC, Geertsema C, Nieuwenhuis N, de Ridder D, Conley ME, et al.

Gross deletions involving IGHM, BTK, or Artemis: A model for genomic lesions mediated by transposable elements

AMERICAN JOURNAL OF HUMAN GENETICS. 2008 FEB; 82 (2): 320-332

173

6317 Baldwin EL, May LE, Justice AN, Martin CL, Ledbetter DH

Mechanisms and consequences of small supernumerary marker chromosomes: From Barbara McClintock to modern genetic-counseling issues

AMERICAN JOURNAL OF HUMAN GENETICS. 2008 FEB; 82 (2): 398-410

174

7025 Firth HV, Richards SM, Bevan AP, Clayton S, Corpas M, et al.

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

AMERICAN JOURNAL OF HUMAN GENETICS. 2009 APR 10; 84 (4): 524-533

175

430 Greendale K, Pyeritz RE

Empowering primary care health professionals in medical genetics: How soon? How fast? How far?

AMERICAN JOURNAL OF MEDICAL GENETICS. 2001 FAL; 106 (3): 223-232

176

1313 Pociot F, Karlsen AE

Combined genome and proteome approach to identify new susceptibility genes

AMERICAN JOURNAL OF MEDICAL GENETICS. 2002 MAY 30; 115 (1): 55-60

177

1705 Goodman FR

Limb malformations and the human HOX genes

AMERICAN JOURNAL OF MEDICAL GENETICS. 2002 OCT 15; 112 (3): 256-265

178

2356 McCormack WM, Shen JJ, Curry SM, Berend SA, Kashork C, et al.

Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation (vol 112, pg 384, 2002)

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 APR 15; 118A (2): 200-+

179

2433 de Pater JM, Smeets DFCM, Scheres JMJC

Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved?

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 MAY 15; 119A (1): 26-31

180

2599 Bannykh SI, Emery SC, Gerber JK, Jones KL, Benirschke K, et al.

Aberrant Pax1 and Pax9 expression in Jarcho-Levin syndrome: Report of two Caucasian siblings and literature review

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 JUL 15; 120A (2): 241-246

Date / Author / Journal

LCS

GCS

LCR

181

2948 Irving M, Hanson H, Turnpenny P, Brewer C, Ogilvie CM, et al.

Deletion of the distal long arm of chromosome 10; Is there a characteristic phenotype? A report of 15 de novo and familial cases

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2003 DEC 1; 123A (2): 153-163

182

4235 Aslam M, Wajid M, Chahrour MH, Ansar M, Haque S, et al.

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 FEB 15; 133A (1): 18-22

183

4236 Mir A, Ansar M, Chahrour MH, Phain TL, Wajid M, et al.

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 FEB 15; 133A (1): 23-26

184

4285 Amor DJ, Voullaire L, Bentley K, Savarirayan R, Amor DJ

Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 MAR 1; 133A (2): 151-157

185

4363 Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, et al.

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 APR 30; 134A (3): 259-267

186

4559 Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, et al.

A report of three patients with an interstitial deletion of chromosome 15q24

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2005 AUG 15; 137A (1): 65-71

187

5008 Zhang LL, Wang T, Wright AF, Suri M, Schwartz CE, et al.

A microdeletion in Xp11.3 accounts for co-segregation of retinitis pigmentosa and mental retardation in a large kindred

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2006 FEB 15; 140A (4): 349-357

188

5766 Barber JCK, Maloney VK, Kirchhoff M, Thomas NS, Boyle TA, et al.

Transmitted duplication of 12q21.32-12q22 includes 48 genes and has no apparent phenotypic consequences

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 MAR 15; 143A (6): 615-618

189

5805 Feldman GJ, Billings PC, Patel RV, Caron RJ, Guenther C, et al.

Over-expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: A new syndrome

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 APR 1; 143A (7): 699-706

190

5922 Probst FJ, Roeder ER, Enciso VB, Ou ZS, Cooper ML, et al.

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007 JUN 15; 143A (12): 1358-1365

Date / Author / Journal

LCS

GCS

LCR

191

6658 Jones JR, Skinner C, Friez MJ, Schwartz CE, Stevenson RE

Hypothesis: Dysregulation of methylation of brain-expressed genes on the X chromosome and autism spectrum disorders

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2008 SEP 1; 146A (17): 2213-2220

104

192

6708 Kulikowski LD, Bellucco FTS, Nogueira SI, Christofolini DM, Smith MDC, et al.

Pure Duplication 1q41-qter: Further Delineation of Trisomy 1q Syndromes

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2008 OCT 15; 146A (20): 2663-2667

193

6919 Misceo D, Rocchi M, van der Hagen CB, Frengen E

A Partial Trisomy 1q Patient With a Deletion 1q22 and an Insertion 1(q42q44) Into 1q22

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2009 FEB; 149A (2): 290-293

194

6704 Neale BM, Purcell S

The Positives, Protocols, and Perils of Genome-Wide Association

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2008 OCT 5; 147B (7): 1288-1294

195

2682 Platte P, Papanicolaou GJ, Johnston J, Klein CM, Doheny KF, et al.

A study of linkage and association of body mass index in the Old Order Amish

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2003 AUG 15; 121C (1): 71-80

196

2886 Schulze TG, McMahon FJ

Genetic linkage and association studies in bipolar affective disorder: A time for optimism

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2003 NOV 15; 123C (1): 36-47

115

197

7071 Haque FN, Gottesman II, Wong AHC

Not Really Identical: Epigenetic Differences in Monozygotic Twins and Implications for Twin Studies in Psychiatry

AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2009 MAY 15; 151C (2): 136-141

198

2357 Crowley WF

Translation of basic research into useful treatments: How often does it occur?

AMERICAN JOURNAL OF MEDICINE. 2003 APR 15; 114 (6): 503-505

199

5686 Pennell CE, Jacobsson B, Williams SM, Buns RM, Muglia LJ, et al.

Genetic epidemiologic studies of preterm birth: guidelines for research

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY. 2007 FEB; 196 (2): 107-118

133

200

2294 Moroi SE, Gokhale PA, Schteingart MT, Sugar A, Downs CA, et al.

Clinicopathologic correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy

AMERICAN JOURNAL OF OPHTHALMOLOGY. 2003 APR; 135 (4): 461-470

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
List of All Records