| Year |
Citation |
Score |
| 2022 |
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, ... ... Herman GE, et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics. PMID 35982160 DOI: 10.1038/s41588-022-01104-0 |
0.31 |
|
| 2019 |
Repnikova EA, Lyalin DA, McDonald K, Astbury C, Hansen-Kiss E, Cooley LD, Pfau R, Herman GE, Pyatt RE, Hickey SE. CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. European Journal of Medical Genetics. PMID 30836150 DOI: 10.1016/J.Ejmg.2019.02.008 |
0.354 |
|
| 2018 |
Islam MP, Herman GE, de Los Reyes EC. Language Regression in an Atypical SLC6A1 Mutation. Seminars in Pediatric Neurology. 26: 25-27. PMID 29961511 DOI: 10.1016/J.Spen.2018.04.001 |
0.407 |
|
| 2018 |
Kumar R, Gardner A, Homan CC, Douglas E, Mefford H, Wieczorek D, Lüdecke HJ, Stark Z, Sadedin S, Nowak CB, Douglas J, Parsons G, Mark P, Loidi L, ... Herman GE, et al. Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery. Human Mutation. PMID 29851191 DOI: 10.1002/Humu.23557 |
0.364 |
|
| 2017 |
Tsutiya A, Nakano Y, Hansen-Kiss E, Kelly B, Nishihara M, Goshima Y, Corsmeier D, White P, Herman GE, Ohtani-Kaneko R. Human CRMP4 mutation and disrupted Crmp4 expression in mice are associated with ASD characteristics and sexual dimorphism. Scientific Reports. 7: 16812. PMID 29196732 DOI: 10.1038/S41598-017-16782-8 |
0.366 |
|
| 2017 |
Hansen-Kiss E, Beinkampen S, Adler B, Frazier T, Prior T, Erdman S, Eng C, Herman G. A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children. Journal of Medical Genetics. PMID 28526761 DOI: 10.1136/Jmedgenet-2016-104484 |
0.379 |
|
| 2017 |
Manolio TA, Fowler DM, Starita LM, Haendel MA, MacArthur DG, Biesecker LG, Worthey E, Chisholm RL, Green ED, Jacob HJ, McLeod HL, Roden D, Rodriguez LL, Williams MS, Cooper GM, ... ... Herman GE, et al. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 169: 6-12. PMID 28340351 DOI: 10.1016/J.Cell.2017.03.005 |
0.319 |
|
| 2016 |
Kalia SS, Adelman K, Bale SJ, Chung WK, Eng C, Evans JP, Herman GE, Hufnagel SB, Klein TE, Korf BR, McKelvey KD, Ormond KE, Richards CS, Vlangos CN, Watson M, et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27854360 DOI: 10.1038/Gim.2016.190 |
0.303 |
|
| 2015 |
Cunningham D, DeBarber AE, Bir N, Binkley L, Merkens LS, Steiner RD, Herman GE. Analysis of hedgehog signaling in cerebellar granule cell precursors in a conditional Nsdhl allele demonstrates an essential role for cholesterol in postnatal CNS development. Human Molecular Genetics. 24: 2808-25. PMID 25652406 DOI: 10.1093/Hmg/Ddv042 |
0.445 |
|
| 2014 |
Shehata L, Simeonov DR, Raams A, Wolfe L, Vanderver A, Li X, Huang Y, Garner S, Boerkoel CF, Thurm A, Herman GE, Tifft CJ, He M, Jaspers NG, Gahl WA. ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination. American Journal of Medical Genetics. Part A. 164: 2892-900. PMID 25251875 DOI: 10.1002/Ajmg.A.36709 |
0.366 |
|
| 2014 |
Marks KC, Banks WR, Cunningham D, Witman PM, Herman GE. Analysis of two candidate genes for Basan syndrome. American Journal of Medical Genetics. Part A. 164: 1188-91. PMID 24664640 DOI: 10.1002/Ajmg.A.36438 |
0.391 |
|
| 2012 |
Herman GE, Kratz L. Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 160: 301-21. PMID 23042573 DOI: 10.1002/Ajmg.C.31340 |
0.31 |
|
| 2012 |
Muller EA, Aradhya S, Atkin JF, Carmany EP, Elliott AM, Chudley AE, Clark RD, Everman DB, Garner S, Hall BD, Herman GE, Kivuva E, Ramanathan S, Stevenson DA, Stockton DW, et al. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. American Journal of Medical Genetics. Part A. 158: 391-9. PMID 22190277 DOI: 10.1002/Ajmg.A.34216 |
0.365 |
|
| 2011 |
Gripp KW, Hopkins E, Sol-Church K, Stabley DL, Axelrad ME, Doyle D, Dobyns WB, Hudson C, Johnson J, Tenconi R, Graham GE, Sousa AB, Heller R, Piccione M, Corsello G, ... Herman GE, et al. Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C American Journal of Medical Genetics, Part A. 155: 706-716. PMID 21438134 DOI: 10.1002/Ajmg.A.33884 |
0.335 |
|
| 2011 |
Cottrell CE, Bir N, Varga E, Alvarez CE, Bouyain S, Zernzach R, Thrush DL, Evans J, Trimarchi M, Butter EM, Cunningham D, Gastier-Foster JM, McBride KL, Herman GE. Contactin 4 as an autism susceptibility locus. Autism Research : Official Journal of the International Society For Autism Research. 4: 189-99. PMID 21308999 DOI: 10.1002/Aur.184 |
0.391 |
|
| 2010 |
McLarren KW, Severson TM, du Souich C, Stockton DW, Kratz LE, Cunningham D, Hendson G, Morin RD, Wu D, Paul JE, An J, Nelson TN, Chou A, DeBarber AE, Merkens LS, ... ... Herman GE, et al. Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome. American Journal of Human Genetics. 87: 905-14. PMID 21129721 DOI: 10.1016/J.Ajhg.2010.11.004 |
0.448 |
|
| 2010 |
McBride KL, Varga EA, Pastore MT, Prior TW, Manickam K, Atkin JF, Herman GE. Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly. Autism Research : Official Journal of the International Society For Autism Research. 3: 137-41. PMID 20533527 DOI: 10.1002/Aur.132 |
0.438 |
|
| 2010 |
Solomon BD, Lange E, Shubrook J, Service FJ, Herman G, Karne RJ, Gorden P, Muenke M, Stratakis CA. Deletion of 8q24 in an adult with mild dysmorphic features, developmental delay, and ketotic hypoglycemia. American Journal of Medical Genetics. Part A. 152: 1545-9. PMID 20503333 DOI: 10.1002/Ajmg.A.33395 |
0.363 |
|
| 2010 |
McGill AK, Pastore MT, Herman GE, Alliman S, Rosenfeld JA, Weaver DD. A tale of two deletions: a report of two novel 20p13 --> pter deletions. American Journal of Medical Genetics. Part A. 152: 1000-7. PMID 20358616 DOI: 10.1002/Ajmg.A.33339 |
0.348 |
|
| 2010 |
Cunningham D, Talabere T, Bir N, Kennedy M, McBride KL, Herman GE. Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos. Human Molecular Genetics. 19: 364-73. PMID 19880419 DOI: 10.1093/Hmg/Ddp502 |
0.333 |
|
| 2009 |
Cunningham D, Spychala K, McLarren KW, Garza LA, Boerkoel CF, Herman GE. Developmental expression pattern of the cholesterogenic enzyme NSDHL and negative selection of NSDHL-deficient cells in the heterozygous Bpa(1H)/+ mouse. Molecular Genetics and Metabolism. 98: 356-66. PMID 19631568 DOI: 10.1016/J.Ymgme.2009.06.016 |
0.326 |
|
| 2009 |
Varga EA, Pastore M, Prior T, Herman GE, McBride KL. The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 111-7. PMID 19265751 DOI: 10.1097/Gim.0B013E31818Fd762 |
0.437 |
|
| 2007 |
Herman GE, Henninger N, Ratliff-Schaub K, Pastore M, Fitzgerald S, McBride KL. Genetic testing in autism: how much is enough? Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 268-74. PMID 17505203 DOI: 10.1097/Gim.0B013E31804D683B |
0.385 |
|
| 2007 |
Herman GE, Butter E, Enrile B, Pastore M, Prior TW, Sommer A. Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly. American Journal of Medical Genetics. Part A. 143: 589-93. PMID 17286265 DOI: 10.1002/Ajmg.A.31619 |
0.417 |
|
| 2006 |
Jiang F, Herman GE. Analysis of Nsdhl-deficient embryos reveals a role for Hedgehog signaling in early placental development. Human Molecular Genetics. 15: 3293-305. PMID 17028112 DOI: 10.1093/Hmg/Ddl405 |
0.406 |
|
| 2005 |
Cunningham D, Swartzlander D, Liyanarachchi S, Davuluri RV, Herman GE. Changes in gene expression associated with loss of function of the NSDHL sterol dehydrogenase in mouse embryonic fibroblasts. Journal of Lipid Research. 46: 1150-62. PMID 15805545 DOI: 10.1194/Jlr.M400462-Jlr200 |
0.444 |
|
| 2005 |
Caldas H, Cunningham D, Wang X, Jiang F, Humphries L, Kelley RI, Herman GE. Placental defects are associated with male lethality in bare patches and striated embryos deficient in the NAD(P)H Steroid Dehydrogenase-like (NSDHL) Enzyme. Molecular Genetics and Metabolism. 84: 48-60. PMID 15639195 DOI: 10.1016/J.Ymgme.2004.08.007 |
0.442 |
|
| 2003 |
Lucas ME, Ma Q, Cunningham D, Peters J, Cattanach B, Bard M, Elmore BK, Herman GE. Identification of two novel mutations in the murine Nsdhl sterol dehydrogenase gene and development of a functional complementation assay in yeast. Molecular Genetics and Metabolism. 80: 227-33. PMID 14567972 DOI: 10.1016/S1096-7192(03)00137-9 |
0.497 |
|
| 2003 |
Caldas H, Herman GE. NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets. Human Molecular Genetics. 12: 2981-91. PMID 14506130 DOI: 10.1093/Hmg/Ddg321 |
0.351 |
|
| 2003 |
Hummel M, Cunningham D, Mullett CJ, Kelley RI, Herman GE. Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene. American Journal of Medical Genetics. Part A. 122: 246-51. PMID 12966526 DOI: 10.1002/Ajmg.A.20248 |
0.416 |
|
| 2003 |
Herman GE. Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes. Human Molecular Genetics. 12: R75-88. PMID 12668600 DOI: 10.1093/Hmg/Ddg072 |
0.329 |
|
| 2003 |
Tsao CY, Herman G, Boué DR, Prior TW, Lo WD, Atkin JF, Rusin J. Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review. Journal of Child Neurology. 18: 62-4. PMID 12661941 DOI: 10.1177/08830738030180011401 |
0.326 |
|
| 2002 |
Herman GE, Kelley RI, Pureza V, Smith D, Kopacz K, Pitt J, Sutphen R, Sheffield LJ, Metzenberg AB. Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome). Genetics in Medicine : Official Journal of the American College of Medical Genetics. 4: 434-8. PMID 12509714 DOI: 10.1097/00125817-200211000-00006 |
0.484 |
|
| 2002 |
McEntagart M, Parsons G, Buj-Bello A, Biancalana V, Fenton I, Little M, Krawczak M, Thomas N, Herman G, Clarke A, Wallgren-Pettersson C. Genotype–phenotype correlations in X-linked myotubular myopathy Neuromuscular Disorders. 12: 939-946. PMID 12467749 DOI: 10.1016/S0960-8966(02)00153-0 |
0.472 |
|
| 2002 |
Cunningham D, Xiao Q, Chatterjee A, Sulik K, Juriloff D, Elder F, Harrison W, Schuster G, Overbeek PA, Herman GE. exma: an X-linked insertional mutation that disrupts forebrain and eye development. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 179-85. PMID 11956759 DOI: 10.1007/S00335-001-2121-Z |
0.454 |
|
| 2002 |
Copley LM, Zhao WD, Kopacz K, Herman GE, Kioschis P, Poustka A, Taudien S, Platzer M. Exclusion of mutations in the MTMR1 gene as a frequent cause of X-linked myotubular myopathy. American Journal of Medical Genetics. 107: 256-8. PMID 11807911 DOI: 10.1002/Ajmg.10135 |
0.652 |
|
| 2002 |
Herman GE, Kopacz K, Zhao W, Mills PL, Metzenberg A, Das S. Characterization of mutations in fifty North American patients with X-linked myotubular myopathy. Human Mutation. 19: 114-21. PMID 11793470 DOI: 10.1002/Humu.10033 |
0.494 |
|
| 2001 |
Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW. Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations. Journal of Medical Genetics. 38: 761-6. PMID 11694548 DOI: 10.1136/Jmg.38.11.761 |
0.437 |
|
| 2001 |
Carrel T, Herman GE, Moore GE, Stanier P. Lack of mutations in ZIC3 in three families with neural tube defects. American Journal of Medical Genetics. 98: 283-5. PMID 11169570 DOI: 10.1002/1096-8628(20010122)98:3<283::Aid-Ajmg1089>3.0.Co;2-G |
0.358 |
|
| 2000 |
Herman GE. X-Linked dominant disorders of cholesterol biosynthesis in man and mouse. Biochimica Et Biophysica Acta. 1529: 357-373. PMID 11111102 DOI: 10.1016/S1388-1981(00)00160-8 |
0.509 |
|
| 2000 |
Carrel T, Purandare SM, Harrison W, Elder F, Fox T, Casey B, Herman GE. The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus. Human Molecular Genetics. 9: 1937-42. PMID 10942421 DOI: 10.1093/Hmg/9.13.1937 |
0.507 |
|
| 2000 |
Mallon AM, Platzer M, Bate R, Gloeckner G, Botcherby MRM, Nordsiek G, Strivens MA, Kioschis P, Dangel A, Cunningham D, Straw RNA, Weston P, Gilbert M, Fernando S, Goodall K, ... ... Herman GE, et al. Comparative genome sequence analysis of the Bpa/Str region in mouse and man Genome Research. 10: 758-775. PMID 10854409 DOI: 10.1101/Gr.10.6.758 |
0.393 |
|
| 2000 |
Aradhya S, Nelson DL, Heiss NS, Poustka A, Woffendin H, Kenwrick S, Esposito T, Ciccodicola A, Bardaro T, D'Urso M, Smahi A, Munnich A, Herman GE, Lewis RA. Human homologue of the murine bare patches/striated gene is not mutated in incontinentia pigmenti type 2. American Journal of Medical Genetics. 91: 241-4. PMID 10756353 DOI: 10.1002/(Sici)1096-8628(20000320)91:3<241::Aid-Ajmg19>3.0.Co;2-J |
0.461 |
|
| 1999 |
Derry JMJ, Gormally E, Means GD, Zhao W, Meindl A, Kelley RI, Boyd Y, Herman GE. Mutations in a Δ8-Δ7 sterol isomerase in the tattered mouse and X- linked dominant chondrodysplasia punctata Nature Genetics. 22: 286-290. PMID 10391218 DOI: 10.1038/10350 |
0.491 |
|
| 1999 |
Liu XY, Dangel AW, Kelley RI, Zhao W, Denny P, Botcherby M, Cattanach B, Peters J, Hunsicker PR, Mallon AM, Strivens MA, Bate R, Miller W, Rhodes M, Brown SD, ... Herman GE, et al. The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase. Nature Genetics. 22: 182-7. PMID 10369263 DOI: 10.1038/9700 |
0.547 |
|
| 1999 |
Herman GE, Finegold M, Zhao W, Gouyon Bd, Metzenberg A. Medical complications in long-term survivors with X-linked myotubular myopathy. The Journal of Pediatrics. 134: 206-214. PMID 9931531 DOI: 10.1016/S0022-3476(99)70417-8 |
0.35 |
|
| 1998 |
Boyd Y, Blair HJ, Cunliffe P, Denny P, Gormally E, Herman GE. Mouse chromosome X Mammalian Genome. 8. PMID 9662637 DOI: 10.1007/S003359900665 |
0.368 |
|
| 1998 |
Botcherby MRM, Strivens MA, Straw R, Williams GW, Fernando S, Mallon AM, Umrania Y, Woollard PM, Gilbert M, Bates R, Goodall K, Greystrong JS, Denny P, Rhodes M, Mundy CR, ... Herman GE, et al. Comparative sequencing on the mouse and human X chromosomes Genetics Research. 72: 59-72. DOI: 10.1017/S0016672398273307 |
0.383 |
|
| 1997 |
Gouyon BMd, Zhao W, Laporte J, Mandel J, Metzenberg A, Herman GE. Characterization of Mutations in the Myotubularin Gene in Twenty Six Patients with X-Linked Myotubular Myopathy Human Molecular Genetics. 6: 1499-1504. PMID 9285787 DOI: 10.1093/Hmg/6.9.1499 |
0.512 |
|
| 1997 |
Heiss NS, Gloeckner G, Bächner D, Kioschis P, Klauck SM, Hinzmann B, Rosenthal A, Herman GE, Poustka A. Genomic structure of a novel LIM domain gene (ZNF185) in Xq28 and comparisons with the orthologous murine transcript Genomics. 43: 329-338. PMID 9268636 DOI: 10.1006/Geno.1997.4810 |
0.394 |
|
| 1997 |
Boyd Y, Herman GE, Avner P, Disteche CM, Adler D, Reed V, Blair HJ. Mouse X chromosome. Mammalian Genome : Official Journal of the International Mammalian Genome Society. S313-26. PMID 9233403 DOI: 10.1007/S003359900332 |
0.424 |
|
| 1996 |
Uwechue IC, Cooper BF, Goble C, Hacker T, Blair HJ, Burke DT, Herman G, Boyd Y. The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization. Genomics. 37: 238-41. PMID 8921395 DOI: 10.1006/Geno.1996.0549 |
0.472 |
|
| 1996 |
Frattini A, Chatterjee A, Faranda S, Sacco MG, Villa A, Herman GE, Vezzoni P. The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue Genomics. 32: 277-280. PMID 8833156 DOI: 10.1006/Geno.1996.0116 |
0.405 |
|
| 1996 |
Levin ML, Chatterjee A, Pragliola A, Worley KC, Wehnert M, Zhuchenko O, Smith RF, Lee CC, Herman GE. A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28. Genome Research. 6: 465-477. PMID 8828036 DOI: 10.1101/Gr.6.6.465 |
0.473 |
|
| 1996 |
Dupuis L, Leon-Del-Rio A, Leclerc D, Campeau E, Sweetman L, Saudubray JM, Herman G, Gibson KM, Gravel RA. Clustering of mutations in the biotin-binding region of holocarboxylase synthetase in biotin-responsive multiple carboxylase deficiency Human Molecular Genetics. 5: 1011-1016. PMID 8817339 DOI: 10.1093/Hmg/5.7.1011 |
0.399 |
|
| 1996 |
Gouyon Bd, Chatterjee A, Monaco A, Quaderi N, Brown SDM, Herman GE. Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region. Mammalian Genome. 7: 575-579. PMID 8678976 DOI: 10.1007/S003359900172 |
0.451 |
|
| 1995 |
Chatterjee A, Tanaka T, Parrish JE, Herman GE. Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mammalian Genome. 6: 802-804. PMID 8597638 DOI: 10.1007/Bf00539008 |
0.454 |
|
| 1995 |
Joseph M, Pai GS, Holden KR, Herman G. X‐linked myotubular myopathy: Clinical observations in ten additional cases American Journal of Medical Genetics. 59: 168-173. PMID 8588581 DOI: 10.1002/Ajmg.1320590211 |
0.343 |
|
| 1995 |
Pasteris NG, Gouyon Bd, Cadle AB, Campbell K, Herman GE, Gorski JL. Cloning and regional localization of the mouse faciogenital dysplasia ( Fgd1 ) gene Mammalian Genome. 6: 658-661. PMID 8535076 DOI: 10.1007/Bf00352375 |
0.356 |
|
| 1995 |
Rivella S, Tamanini F, Bione S, Mancini M, Herman G, Chatterjee A, Maestrini E, Toniolo D. A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes. Genomics. 28: 377-82. PMID 7490070 DOI: 10.1006/Geno.1995.1164 |
0.428 |
|
| 1994 |
Chatterjee A, Faust CJ, Molinari-Storey L, Kiochis P, Poustka A, Herman GE. A 2.3-Mb yeast artificial chromosome contig spanning from Gabra3 to G6pd on the mouse X chromosome. Genomics. 21: 49-57. PMID 8088815 DOI: 10.1006/Geno.1994.1223 |
0.379 |
|
| 1994 |
Quaderi NA, Meehan RR, Tate PH, Cross SH, Bird AP, Chatterjee A, Herman GE, Brown SDM. Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome. Genomics. 22: 648-651. PMID 8001979 DOI: 10.1006/Geno.1994.1442 |
0.42 |
|
| 1994 |
Dahl N, Samson F, Thomas NST, Hu LJ, Gong W, Herman G, Laporte J, Kioschis P, Poustka A, Mandel JL. X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684) Journal of Medical Genetics. 31: 922-924. PMID 7891372 DOI: 10.1136/Jmg.31.12.922 |
0.396 |
|
| 1994 |
Rogner UC, Kioschis P, Wilke K, Gong W, Pick E, Dietrich A, Zechner U, Hameister H, Pragllola A, Herman GE, Yates JRW, Lehrach H, Poustka A. A YAC clone map spanning 7.5 megabases of human chromosome band Xq28 Human Molecular Genetics. 3: 2137-2146. PMID 7881410 DOI: 10.1093/Hmg/3.12.2137 |
0.388 |
|
| 1993 |
Faust CJ, Gonzales JC, Seibold A, Birnbaumer M, Herman GE. Comparative mapping on the mouse and human X chromosomes of a human cDNA clone encoding the vasopressin renal-type receptor (AVP2R) Genomics. 15: 439-441. PMID 8449515 DOI: 10.1006/Geno.1993.1085 |
0.404 |
|
| 1993 |
Angel TA, Faust CJ, Gonzales JC, Kenwrick S, Lewis RA, Herman GE. Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 171-6. PMID 8439729 DOI: 10.1007/Bf00352233 |
0.539 |
|
| 1993 |
Daniele A, Faust CJ, Herman GE, Di Natale P, Ballabio A. Cloning and characterization of the cDNA for the murine iduronate sulfatase gene. Genomics. 16: 755-7. PMID 8325651 DOI: 10.1006/Geno.1993.1259 |
0.393 |
|
| 1993 |
Chatterjee A, Faust CJ, Herman GE. Genetic and physical mapping of the biglycan gene on the mouse X chromosome. Mammalian Genome. 4: 33-36. PMID 8093671 DOI: 10.1007/Bf00364660 |
0.429 |
|
| 1992 |
Faust CJ, Verkerk AJMH, Wilson PJ, Morris CP, Hopwood JJ, Oostra BA, Herman GE. Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes. Genomics. 12: 814-817. PMID 1572654 DOI: 10.1016/0888-7543(92)90314-I |
0.477 |
|
| 1992 |
Faust CJ, Levinson B, Gitschier J, Herman GE. Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage Genomics. 13: 1289-1295. PMID 1354645 DOI: 10.1016/0888-7543(92)90048-W |
0.427 |
|
| 1991 |
Herman GE, Berry M, Munro E, Craig IW, Levy ER. The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction. Genomics. 10: 961-70. PMID 1916827 DOI: 10.1016/0888-7543(91)90186-I |
0.345 |
|
| 1991 |
Faust CJ, Herman GE. Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28 Genomics. 11: 154-164. PMID 1684949 DOI: 10.1016/0888-7543(91)90112-R |
0.39 |
|
| 1991 |
Herman GE, Faust CJ, Darlison MG, Barnard EA. Genetic mapping of the mouse X chromosome in the region homologous to human Xq27-Xq28. Genomics. 9: 670-7. PMID 1674728 DOI: 10.1016/0888-7543(91)90360-Q |
0.418 |
|
| 1990 |
Arn PH, Hauser ER, Thomas GH, Herman G, Hess D, Brusilow SW. Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma. The New England Journal of Medicine. 322: 1652-5. PMID 2342525 DOI: 10.1056/Nejm199006073222307 |
0.421 |
|
| 1990 |
Herman GE, Walton SJ. Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics. 7: 307-312. PMID 1973136 DOI: 10.1016/0888-7543(90)90162-N |
0.493 |
|
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