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Nathan Ellis

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.8 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Ouyang Karen J; Woo Leslie L; Zhu Jianmei; Huo Dezheng; Matunis Michael J; Ellis Nathan A
SUMO modification regulates BLM and RAD51 interaction at damaged replication forks.
Kupfer Sonia S; Torres Jada Benn; Hooker Stanley; Anderson Jeffrey R; Skol Andrew D; Ellis Nathan A; Kittles Rick A
Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans.
Ellis N A; Sander M; Harris C C; Bohr V A
Bloom's syndrome workshop focuses on the functional specificities of RecQ helicases.

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All Publications

2009: Ouyang Karen J; Woo Leslie L; Zhu Jianmei; Huo Dezheng; Matunis Michael J; Ellis Nathan A
SUMO modification regulates BLM and RAD51 interaction at damaged replication forks.
PLoS biology 2009;7(12):e1000252.
2009: Kupfer Sonia S; Torres Jada Benn; Hooker Stanley; Anderson Jeffrey R; Skol Andrew D; Ellis Nathan A; Kittles Rick A
Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans.
Carcinogenesis 2009;30(8):1353-7.
2008: Ellis N A; Sander M; Harris C C; Bohr V A
Bloom's syndrome workshop focuses on the functional specificities of RecQ helicases.
Mechanisms of ageing and development 2008;129(11):681-91.
2008: Zhu Jianmei; Zhu Shanshan; Guzzo Catherine M; Ellis Nathan A; Sung Ki Sa; Choi Cheol Yong; Matunis Michael J
Small ubiquitin-related modifier (SUMO) binding determines substrate recognition and paralog-selective SUMO modification.
The Journal of biological chemistry 2008;283(43):29405-15.
2008: Ellis Nathan A; Huo Dezheng; Yildiz Ozlem; Worrillow Lisa J; Banerjee Mekhala; Le Beau Michelle M; Larson Richard A; Allan James M; Onel Kenan
MDM2 SNP309 and TP53 Arg72Pro interact to alter therapy-related acute myeloid leukemia susceptibility.
Blood 2008;112(3):741-9.
2008: Ouyang Karen J; Woo Leslie L; Ellis Nathan A
Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases.
Mechanisms of ageing and development 2008;129(7-8):425-40.
2008: Gold Bert; Kirchhoff Tomas; Stefanov Stefan; Lautenberger James; Viale Agnes; Garber Judy; Friedman Eitan; Narod Steven; Olshen Adam B; Gregersen Peter; Kosarin Kristi; Olsh Adam; Bergeron Julie; Ellis Nathan A; Klein Robert J; Clark Andrew G; Norton Larry; Dean Michael; Boyd Jeff; Offit Kenneth
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(11):4340-5.
2008: Olshen Adam B; Gold Bert; Lohmueller Kirk E; Struewing Jeffery P; Satagopan Jaya; Stefanov Stefan A; Eskin Eleazar; Kirchhoff Tomas; Lautenberger James A; Klein Robert J; Friedman Eitan; Norton Larry; Ellis Nathan A; Viale Agnes; Lee Catherine S; Borgen Patrick I; Clark Andrew G; Offit Kenneth; Boyd Jeff
Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping.
BMC genetics 2008;9():14.
2007: German James; Sanz Maureen M; Ciocci Susan; Ye Tian Z; Ellis Nathan A
Syndrome-causing mutations of the BLM gene in persons in the Bloom's Syndrome Registry.
Human mutation 2007;28(8):743-53.
2007: Guillem Jose G; Glogowski Emily; Moore Harvey G; Nafa Khedoudja; Markowitz Arnold J; Shia Jinru; Offit Kenneth; Ellis Nathan A
Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.
Annals of surgery 2007;245(4):560-5.
2007: Pereira Lutécia H Mateus; Pineda Marbin A; Rowe William H; Fonseca Libia R; Greene Mark H; Offit Kenneth; Ellis Nathan A; Zhang Jinghui; Collins Andrew; Struewing Jeffery P
The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies.
BMC genetics 2007;8():68.
2007: Woo Leslie L; Onel Kenan; Ellis Nathan A
The broken genome: genetic and pharmacologic approaches to breaking DNA.
Annals of medicine 2007;39(3):208-18.
2006: Matunis Michael J; Zhang Xiang-Dong; Ellis Nathan A
SUMO: the glue that binds.
Developmental cell 2006;11(5):596-7.
2006: Peterlongo Paolo; Mitra Nandita; Sanchez de Abajo Ana; de la Hoya Miguel; Bassi Chiara; Bertario Lucio; Radice Paolo; Glogowski Emily; Nafa Khedoudja; Caldes Trinidad; Offit Kenneth; Ellis Nathan A
Increased frequency of disease-causing MYH mutations in colon cancer families.
Carcinogenesis 2006;27(11):2243-9.
2006: Chen Sining; Wang Wenyi; Lee Shing; Nafa Khedoudja; Lee Johanna; Romans Kathy; Watson Patrice; Gruber Stephen B; Euhus David; Kinzler Kenneth W; Jass Jeremy; Gallinger Steven; Lindor Noralane M; Casey Graham; Ellis Nathan; Giardiello Francis M; Offit Kenneth; Parmigiani Giovanni;
Prediction of germline mutations and cancer risk in the Lynch syndrome.
JAMA : the journal of the American Medical Association 2006;296(12):1479-87.
2006: Ellis Nathan A; Kirchhoff Tomas; Mitra Nandita; Ye Tian-Zhang; Chuai Shaokun; Huang Helen; Nafa Khedoudja; Norton Larry; Neuhausen Susan; Gordon Derek; Struewing Jeffery P; Narod Steven; Offit Kenneth
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.
Genetic epidemiology 2006;30(1):48-61.
2005: Bian Yansong; Caldes Trinidad; Wijnen Juul; Franken Patrick; Vasen Hans; Kaklamani Virginia; Nafa Khédoudja; Peterlongo Paolo; Ellis Nathan; Baron John A; Burn John; Moeslein Gabriela; Morrison Patrick J; Chen Yu; Ahsan Habibul; Watson Patrice; Lynch Henry T; de la Chapelle Albert; Fodde Riccardo; Pasche Boris
TGFBR1*6A may contribute to hereditary colorectal cancer.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2005;23(13):3074-8.
2005: Peterlongo Paolo; Howe Louise R; Radice Paolo; Sala Paola; Hong Young-Joon; Hong Seok-Il; Mitra Nandita; Offit Kenneth; Ellis Nathan A
Germline mutations of AXIN2 are not associated with nonsyndromic colorectal cancer.
Human mutation 2005;25(5):498-500.
2005: Eladad Sonia; Ye Tian-Zhang; Hu Peng; Leversha Margaret; Beresten Sergey; Matunis Michael J; Ellis Nathan A
Intra-nuclear trafficking of the BLM helicase to DNA damage-induced foci is regulated by SUMO modification.
Human molecular genetics 2005;14(10):1351-65.
2005: Peterlongo Paolo; Mitra Nandita; Chuai Shaokun; Kirchhoff Tomas; Palmer Crystal; Huang Helen; Nafa Khedoudja; Offit Kenneth; Ellis Nathan A
Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH.
International journal of cancer. Journal international du cancer 2005;114(3):505-7.
2005: Shaag Avraham; Walsh Tom; Renbaum Paul; Kirchhoff Tomas; Nafa Khedoudja; Shiovitz Stacey; Mandell Jessica B; Welcsh Piri; Lee Ming K; Ellis Nathan; Offit Kenneth; Levy-Lahad Ephrat; King Mary-Claire
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.
Human molecular genetics 2005;14(4):555-63.
2005: Shia Jinru; Klimstra David S; Nafa Khedoudja; Offit Kenneth; Guillem Jose G; Markowitz Arnold J; Gerald William L; Ellis Nathan A
Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms.
The American journal of surgical pathology 2005;29(1):96-104.
2005: Siddiqui Rina; Onel Kenan; Facio Flavia; Nafa Kedoudja; Diaz Louis Robles; Kauff Noah; Huang Helen; Robson Mark; Ellis Nathan; Offit Kenneth
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li-Fraumeni-like kindreds.
Familial cancer 2005;4(2):177-81.
2004: Gold Bert; Kalush Francis; Bergeron Julie; Scott Kevin; Mitra Nandita; Wilson Kelly; Ellis Nathan; Huang Helen; Chen Michael; Lippert Ross; Halldorsson Bjarni V; Woodworth Beth; White Thomas; Clark Andrew G; Parl Fritz F; Broder Samuel; Dean Michael; Offit Kenneth
Estrogen receptor genotypes and haplotypes associated with breast cancer risk.
Cancer research 2004;64(24):8891-900.
2004: Mitra Nandita; Ye Tian-Zhang; Smith Alex; Chuai Shaokun; Kirchhoff Tomas; Peterlongo Paolo; Nafa Khedoudja; Phillips Michael S; Offit Kenneth; Ellis Nathan A
Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping.
Cancer research 2004;64(21):8116-25.
2004: Shia Jinru; Ellis Nathan A; Klimstra David S
The utility of immunohistochemical detection of DNA mismatch repair gene proteins.
Virchows Archiv : an international journal of pathology 2004;445(5):431-41.
2004: Kaklamani Virginia; Baddi Lisa; Rosman Diana; Liu Junjian; Ellis Nathan; Oddoux Carole; Ostrer Harry; Chen Yu; Ahsan Habibul; Offit Kenneth; Pasche Boris
No major association between TGFBR1*6A and prostate cancer.
BMC genetics 2004;5():28.
2004: Kirchhoff Tomas; Kauff Noah D; Mitra Nandita; Nafa Kedoudja; Huang Helen; Palmer Crystal; Gulati Tony; Wadsworth Eve; Donat Sheri; Robson Mark E; Ellis Nathan A; Offit Kenneth
BRCA mutations and risk of prostate cancer in Ashkenazi Jews.
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(9):2918-21.
2004: Robson Mark E; Glogowski Emily; Sommer Gunhild; Antonescu Cristina R; Nafa Khedoudja; Maki Robert G; Ellis Nathan; Besmer Peter; Brennan Murray; Offit Kenneth
Pleomorphic characteristics of a germ-line KIT mutation in a large kindred with gastrointestinal stromal tumors, hyperpigmentation, and dysphagia.
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(4):1250-4.
2004: Pasche Boris; Kaklamani Virginia; Hou Nanjiang; Young Taya; Rademaker Alfred; Peterlongo Paolo; Ellis Nathan; Offit Kenneth; Caldes Trinidad; Reiss Michael; Zheng Tongzhang
TGFBR1*6A and cancer: a meta-analysis of 12 case-control studies.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2004;22(4):756-8.
2004: Kirchhoff Tomas; Satagopan Jaya M; Kauff Noah D; Huang Helen; Kolachana Prema; Palmer Crystal; Rapaport Hannah; Nafa Khedoudja; Ellis Nathan A; Offit Kenneth
Frequency of BRCA1 and BRCA2 mutations in unselected Ashkenazi Jewish patients with colorectal cancer.
Journal of the National Cancer Institute 2004;96(1):68-70.
2004: Guillem Jose G; Moore Harvey G; Palmer Crystal; Glogowski Emily; Finch Rob; Nafa Khedoudja; Markowitz Arnold J; Offit Kenneth; Ellis Nathan A
A636P testing in Ashkenazi Jews.
Familial cancer 2004;3(3-4):223-7.
2003: Shia Jinru; Ellis Nathan A; Paty Philip B; Nash Garrett M; Qin Jing; Offit Kenneth; Zhang Xin-Min; Markowitz Arnold J; Nafa Khedoudja; Guillem Jose G; Wong W Douglas; Gerald William L; Klimstra David S
Value of histopathology in predicting microsatellite instability in hereditary nonpolyposis colorectal cancer and sporadic colorectal cancer.
The American journal of surgical pathology 2003;27(11):1407-17.
2003: Peterlongo Paolo; Nafa Khedoudja; Lerman Gabriel S; Glogowski Emily; Shia Jinru; Ye Tian Z; Markowitz Arnold J; Guillem José G; Kolachana Prema; Boyd Jeffrey A; Offit Kenneth; Ellis Nathan A
MSH6 germline mutations are rare in colorectal cancer families.
International journal of cancer. Journal international du cancer 2003;107(4):571-9.
2003: Offit Kenneth; Levran Orna; Mullaney Brian; Mah Katherine; Nafa Khedoudja; Batish Sat Dev; Diotti Raffaella; Schneider Hildegard; Deffenbaugh Amie; Scholl Thomas; Proud Virginia K; Robson Mark; Norton Larry; Ellis Nathan; Hanenberg Helmut; Auerbach Arleen D
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.
Journal of the National Cancer Institute 2003;95(20):1548-51.
2003: Sengupta Sagar; Linke Steven P; Pedeux Remy; Yang Qin; Farnsworth Julie; Garfield Susan H; Valerie Kristoffer; Shay Jerry W; Ellis Nathan A; Wasylyk Bohdan; Harris Curtis C
BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination.
The EMBO journal 2003;22(5):1210-22.
2003: Guillem José G; Rapaport Beth S; Kirchhoff Tomas; Kolachana Prema; Nafa Khedoudja; Glogowski Emily; Finch Rob; Huang Helen; Foulkes William D; Markowitz Arnold; Ellis Nathan A; Offit Kenneth
A636P is associated with early-onset colon cancer in Ashkenazi Jews.
Journal of the American College of Surgeons 2003;196(2):222-5.
2003: Offit Kenneth; Pierce Heather; Kirchhoff Tomas; Kolachana Prema; Rapaport Beth; Gregersen Peter; Johnson Steven; Yossepowitch Orit; Huang Helen; Satagopan Jaya; Robson Mark; Scheuer Lauren; Nafa Khedoudja; Ellis Nathan
Frequency of CHEK2*1100delC in New York breast cancer cases and controls.
BMC medical genetics 2003;4():1.
2002: Offit Kenneth; Gilad Shlomit; Paglin Shoshana; Kolachana Prema; Roisman Laila C; Nafa Khedoudja; Yeugelewitz Vincent; Gonzales Maria; Robson Mark; McDermott Deborah; Pierce Heather Hanson; Kauff Noah D; Einat Paz; Jhanwar Suresh; Satagopan Jaya M; Oddoux Carole; Ellis Nathan; Skaliter Rami; Yahalom Joachim
Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers.
Clinical cancer research : an official journal of the American Association for Cancer Research 2002;8(12):3813-9.
2002: Foulkes W D; Thiffault I; Gruber S B; Horwitz M; Hamel N; Lee C; Shia J; Markowitz A; Figer A; Friedman E; Farber D; Greenwood C M T; Bonner J D; Nafa K; Walsh T; Marcus V; Tomsho L; Gebert J; Macrae F A; Gaff C L; Paillerets B Bressac-De; Gregersen P K; Weitzel J N; Gordon P H; MacNamara E; King M-C; Hampel H; De La Chapelle A; Boyd J; Offit K; Rennert G; Chong G; Ellis N A
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.
American journal of human genetics 2002;71(6):1395-412.
2002: Gruber Stephen B; Ellis Nathan A; Scott Karen K; Almog Ronit; Kolachana Prema; Bonner Joseph D; Kirchhoff Tomas; Tomsho Lynn P; Nafa Khedoudja; Pierce Heather; Low Marcelo; Satagopan Jaya; Rennert Hedy; Huang Helen; Greenson Joel K; Groden Joanna; Rapaport Beth; Shia Jinru; Johnson Stephen; Gregersen Peter K; Harris Curtis C; Boyd Jeff; Rennert Gad; Offit Kenneth
BLM heterozygosity and the risk of colorectal cancer.
Science (New York, N.Y.) 2002;297(5589):2013.
2002: Teruya-Feldstein J; Greene J; Cohen L; Popplewell L; Ellis Nathan A; Offit K
Analysis of mismatch repair defects in the familial occurrence of lymphoma and colorectal cancer.
Leukemia & lymphoma 2002;43(8):1619-26.
2002: Kauff N D; Perez-Segura P; Robson M E; Scheuer L; Siegel B; Schluger A; Rapaport B; Frank T S; Nafa K; Ellis N A; Parmigiani G; Offit K
Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families.
Journal of medical genetics 2002;39(8):611-4.
2002: Beamish Heather; Kedar Padmini; Kaneko Hideo; Chen Philip; Fukao Toshiyuki; Peng Cheng; Beresten Sergei; Gueven Nuri; Purdie David; Lees-Miller Susan; Ellis Nathan; Kondo Naomi; Lavin Martin F
Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM.
The Journal of biological chemistry 2002;277(34):30515-23.
2002: Stark Jeremy M; Hu Peng; Pierce Andrew J; Moynahan Mary Ellen; Ellis Nathan; Jasin Maria
ATP hydrolysis by mammalian RAD51 has a key role during homology-directed DNA repair.
The Journal of biological chemistry 2002;277(23):20185-94.
2002: Kauff Noah D; Satagopan Jaya M; Robson Mark E; Scheuer Lauren; Hensley Martee; Hudis Clifford A; Ellis Nathan A; Boyd Jeff; Borgen Patrick I; Barakat Richard R; Norton Larry; Castiel Mercedes; Nafa Khedoudja; Offit Kenneth
Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation.
The New England journal of medicine 2002;346(21):1609-15.
2002: Scheuer Lauren; Kauff Noah; Robson Mark; Kelly Bridget; Barakat Richard; Satagopan Jaya; Ellis Nathan; Hensley Martee; Boyd Jeff; Borgen Patrick; Norton Larry; Offit Kenneth
Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2002;20(5):1260-8.
2002: Robson M; Scheuer L; Nafa K; Ellis N; Offit K
Unique de novo mutation of BRCA2 in a woman with early onset breast cancer.
Journal of medical genetics 2002;39(2):126-8.
2001: Pierce A J; Hu P; Han M; Ellis N; Jasin M
Ku DNA end-binding protein modulates homologous repair of double-strand breaks in mammalian cells.
Genes & development 2001;15(24):3237-42.
2001: Wang X W; Tseng A; Ellis N A; Spillare E A; Linke S P; Robles A I; Seker H; Yang Q; Hu P; Beresten S; Bemmels N A; Garfield S; Harris C C
Functional interaction of p53 and BLM DNA helicase in apoptosis.
The Journal of biological chemistry 2001;276(35):32948-55.
2001: Hu P; Beresten S F; van Brabant A J; Ye T Z; Pandolfi P P; Johnson F B; Guarente L; Ellis N A
Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability.
Human molecular genetics 2001;10(12):1287-98.
2001: Bischof O; Kim S H; Irving J; Beresten S; Ellis N A; Campisi J
Regulation and localization of the Bloom syndrome protein in response to DNA damage.
The Journal of cell biology 2001;153(2):367-80.
2001: Ellis N A; Ciocci S; German J
Back mutation can produce phenotype reversion in Bloom syndrome somatic cells.
Human genetics 2001;108(2):167-73.
2000: van Brabant A J; Ye T; Sanz M; German III J L; Ellis N A; Holloman W K
Binding and melting of D-loops by the Bloom syndrome helicase.
Biochemistry 2000;39(47):14617-25.
2000: Kawabe T; Tsuyama N; Kitao S; Nishikawa K; Shimamoto A; Shiratori M; Matsumoto T; Anno K; Sato T; Mitsui Y; Seki M; Enomoto T; Goto M; Ellis N A; Ide T; Furuichi Y; Sugimoto M
Differential regulation of human RecQ family helicases in cell transformation and cell cycle.
Oncogene 2000;19(41):4764-72.
2000: Huang S; Beresten S; Li B; Oshima J; Ellis N A; Campisi J
Characterization of the human and mouse WRN 3'-->5' exonuclease.
Nucleic acids research 2000;28(12):2396-405.
2000: Johnson F B; Lombard D B; Neff N F; Mastrangelo M A; Dewolf W; Ellis N A; Marciniak R A; Yin Y; Jaenisch R; Guarente L
Association of the Bloom syndrome protein with topoisomerase IIIalpha in somatic and meiotic cells.
Cancer research 2000;60(5):1162-7.
2000: van Brabant A J; Stan R; Ellis N A
DNA helicases, genomic instability, and human genetic disease.
Annual review of genomics and human genetics 2000;1():409-59.
2000: Sanz M M; Proytcheva M; Ellis N A; Holloman W K; German J
BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins.
Cytogenetics and cell genetics 2000;91(1-4):217-23.
1999: Zhong S; Hu P; Ye T Z; Stan R; Ellis N A; Pandolfi P P
A role for PML and the nuclear body in genomic stability.
Oncogene 1999;18(56):7941-7.
1999: Beresten S F; Stan R; van Brabant A J; Ye T; Naureckiene S; Ellis N A
Purification of overexpressed hexahistidine-tagged BLM N431 as oligomeric complexes.
Protein expression and purification 1999;17(2):239-48.
1999: Ellis N A; Proytcheva M; Sanz M M; Ye T Z; German J
Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal.
American journal of human genetics 1999;65(5):1368-74.
1999: Neff N F; Ellis N A; Ye T Z; Noonan J; Huang K; Sanz M; Proytcheva M
The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells.
Molecular biology of the cell 1999;10(3):665-76.
1998: Ellis N A; Ciocci S; Proytcheva M; Lennon D; Groden J; German J
The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry.
American journal of human genetics 1998;63(6):1685-93.
1998: Tippett P; Ellis N A
The Xg blood group system: a review.
Transfusion medicine reviews 1998;12(4):233-57.
1998: Ellis N A
The war of the sex chromosomes.
Nature genetics 1998;20(1):9-10.
1998: Li L; Eng C; Desnick R J; German J; Ellis N A
Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.
Molecular genetics and metabolism 1998;64(4):286-90.
1998: Straughen J E; Johnson J; McLaren D; Proytcheva M; Ellis N; German J; Groden J
A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene.
Human mutation 1998;11(2):175-8.
1997: Ellis N A
DNA helicases in inherited human disorders.
Current opinion in genetics & development 1997;7(3):354-63.
1996: Straughen J; Ciocci S; Ye T Z; Lennon D N; Proytcheva M; Alhadeff B; Goodfellow P; German J; Ellis N A; Groden J
Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1.
Genomics 1996;35(1):118-28.
1996: German J; Ellis N A; Proytcheva M
Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity.
Clinical genetics 1996;49(5):223-31.
1996: Ellis N A
Mutation-causing mutations.
Nature 1996;381(6578):110-1.
1996: Ellis N A; German J
Molecular genetics of Bloom's syndrome.
Human molecular genetics 1996;5 Spec No():1457-63.
1996: Affara N; Bishop C; Brown W; Cooke H; Davey P; Ellis N; Graves J M; Jones M; Mitchell M; Rappold G; Tyler-Smith C; Yen P; Lau Y F
Report of the Second International Workshop on Y Chromosome Mapping 1995.
Cytogenetics and cell genetics 1996;73(1-2):33-76.
1995: Ellis N A; Groden J; Ye T Z; Straughen J; Lennon D J; Ciocci S; Proytcheva M; German J
The Bloom's syndrome gene product is homologous to RecQ helicases.
Cell 1995;83(4):655-66.
1995: Ellis N A; Lennon D J; Proytcheva M; Alhadeff B; Henderson E E; German J
Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells.
American journal of human genetics 1995;57(5):1019-27.
1995: Ellis N A
Ecce Ohno!
Nature genetics 1995;10(4):373-5.
1995: Weller P A; Critcher R; Goodfellow P N; German J; Ellis N A
The human Y chromosome homologue of XG: transcription of a naturally truncated gene.
Human molecular genetics 1995;4(5):859-68.
1994: Ellis N A; Tippett P; Petty A; Reid M; Weller P A; Ye T Z; German J; Goodfellow P N; Thomas S; Banting G
PBDX is the XG blood group gene.
Nature genetics 1994;8(3):285-90.
1994: Ellis N A; Roe A M; Kozloski J; Proytcheva M; Falk C; German J
Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.
American journal of human genetics 1994;55(3):453-60.
1994: German J; Roe A M; Leppert M F; Ellis N A
Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(14):6669-73.
1994: Ellis N A; Ye T Z; Patton S; German J; Goodfellow P N; Weller P
Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp.
Nature genetics 1994;6(4):394-400.
1990: Ellis N; Yen P; Neiswanger K; Shapiro L J; Goodfellow P N
Evolution of the pseudoautosomal boundary in Old World monkeys and great apes.
Cell 1990;63(5):977-86.
1990: Ellis N; Kidd J; Goodfellow P J; Kidd K; Goodfellow P N
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary.
American journal of human genetics 1990;46(5):950-5.
1990: Ellis N; Taylor A; Bengtsson B O; Kidd J; Rogers J; Goodfellow P
Population structure of the human pseudoautosomal boundary.
Nature 1990;344(6267):663-5.
1989: Ellis N; Goodfellow P N
The mammalian pseudoautosomal region.
Trends in genetics : TIG 1989;5(12):406-10.
1989: Palmer M S; Sinclair A H; Berta P; Ellis N A; Goodfellow P N; Abbas N E; Fellous M
Genetic evidence that ZFY is not the testis-determining factor.
Nature 1989;342(6252):937-9.
1989: Ellis N A; Goodfellow P J; Pym B; Smith M; Palmer M; Frischauf A M; Goodfellow P N
The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome.
Nature 1989;337(6202):81-4.
1988: Goodfellow P N; Pym B; Pritchard C; Ellis N; Palmer M; Smith M; Goodfellow P J
MIC2: a human pseudoautosomal gene.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;322(1208):145-54.
1988: Hansen R S; Ellis N A; Gartler S M
Demethylation of specific sites in the 5' region of the inactive X-linked human phosphoglycerate kinase gene correlates with the appearance of nuclease sensitivity and gene expression.
Molecular and cellular biology 1988;8(11):4692-9.
1988: Adra C N; Ellis N A; McBurney M W
The family of mouse phosphoglycerate kinase genes and pseudogenes.
Somatic cell and molecular genetics 1988;14(1):69-81.
1987: Ellis N; Keitges E; Gartler S M; Rocchi M
High-frequency reactivation of X-linked genes in Chinese hamster X human hybrid cells.
Somatic cell and molecular genetics 1987;13(3):191-204.
1983: Carothers A M; Urlaub G; Ellis N; Chasin L A
Structure of the dihydrofolate reductase gene in Chinese hamster ovary cells.
Nucleic acids research 1983;11(7):1997-2012.
1982: Ellis N; Gallant J
An estimate of the global error frequency in translation.
Molecular & general genetics : MGG 1982;188(2):169-72.

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