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Successful umbilical cord blood transplantation for Fanconi anemia using preimplantation genetic diagnosis for HLA-matched donorBIELORAI, Bella; HUGHES, Mark R; AUERBACH, Arleen D et al.American journal of hematology. 2004, Vol 77, Num 4, pp 397-399, issn 0361-8609, 3 p.Article

A 20-year perspective on the International Fanconi Anemia Registry (IFAR)KUTLER, David I; SINGH, Bhuvanesh; SATAGOPAN, Jaya et al.Blood. 2003, Vol 101, Num 4, pp 1249-1256, issn 0006-4971, 8 p.Article

Matched sibling donor haematopoietic stem cell transplantation in fanconi anaemia : an update of the Cincinnati Children's experienceFARZIN, Azadeh; DAVIES, Stella M; SMITH, Franklin O et al.British journal of haematology. 2007, Vol 136, Num 4, pp 633-640, issn 0007-1048, 8 p.Article

Successful engraftment without radiation after fludarabine-based regimen in fanconi anemia patients undergoing genotypically identical donor hematopoietic cell transplantationTAN, Poh-Lin; WAGNER, John E; AUERBACH, Arleen D et al.Pediatric blood & cancer. 2006, Vol 46, Num 5, pp 630-636, issn 1545-5009, 7 p.Article

Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4KIM, Yonghwan; SPITZ, Gabriella S; VETURI, Uma et al.Blood. 2013, Vol 121, Num 1, pp 54-63, issn 0006-4971, 10 p.Article

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemiaLEVRAN, Orna; ATTWOOLL, Claire; OTT, Jurg et al.Nature genetics. 2005, Vol 37, Num 9, pp 931-933, issn 1061-4036, 3 p.Article

GST genotype may modify clinical phenotype in patients with Fanconi anaemiaDAVIES, Stella M; RADLOFF, Gretchen A; DEFOR, Todd E et al.British journal of haematology. 2005, Vol 131, Num 1, pp 118-122, issn 0007-1048, 5 p.Article

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutationsCASTELLA, Maria; PUJOL, Roser; PORTO, Beatriz et al.Blood. 2011, Vol 117, Num 14, pp 3759-3769, issn 0006-4971, 11 p.Article

Hypomorphic mutations in the gene encoding a key fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotypeKALB, Reinhard; NEVELING, Kornelia; CASADO, José A et al.American journal of human genetics. 2007, Vol 80, Num 5, pp 895-910, issn 0002-9297, 16 p.Article

Postoperative Clinical Radiosensitivity in Patients With Fanconi Anemia and Head and Neck Squamous Cell CarcinomaBIRKELAND, Andrew C; AUERBACH, Arleen D; SANBORN, Erica et al.Archives of otolaryngology, head & neck surgery. 2011, Vol 137, Num 9, pp 930-934, issn 0886-4470, 5 p.Article

Human papillomavirus DNA and p53 polymorphisms in squamous cell carcinomas from Fanconi anemia patientsKUTLER, David I; WREESMANN, Volkert B; DIOTTI, Rafaella et al.Journal of the National Cancer Institute. 2003, Vol 95, Num 22, pp 1718-1721, issn 0027-8874, 4 p.Article

Evaluation of growth and hormonal status in patients referred to the international Fanconi anemia registryWAJNRAJCH, Michael P; GERTNER, Joseph M; AUERBACH, Arleen D et al.Pediatrics (Evanston). 2001, Vol 107, Num 4, pp 744-754, issn 0031-4005, 1Article

Correct mRNA Processing at a Mutant TT Splice Donor in FANCC Ameliorates the Clinical Phenotype in Patients and Is Enhanced by Delivery of Suppressor U1 snRNAsHARTMANN, Linda; NEVELING, Kornelia; SCHINDLER, Detlev et al.American journal of human genetics. 2010, Vol 87, Num 4, pp 480-493, issn 0002-9297, 14 p.Article

Genetic heterogeneity among fanconi anemia heterozygotes and risk of cancerBERWICK, Marianne; SATAGOPAN, Jaya M; DEV BATISH, Sat et al.Cancer research (Baltimore). 2007, Vol 67, Num 19, pp 9591-9596, issn 0008-5472, 6 p.Article

Unrelated donor bone marrow transplantation for the treatment of Fanconi anemiaWAGNER, John E; EAPEN, Mary; MACMILLAN, Margaret L et al.Blood. 2007, Vol 109, Num 5, pp 2256-2262, issn 0006-4971, 7 p.Article

Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemiaOFFIT, Kenneth; LEVRAN, Orna; PROUD, Virginia K et al.Journal of the National Cancer Institute. 2003, Vol 95, Num 20, pp 1548-1551, issn 0027-8874, 4 p.Article

High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemiaKUTLER, David I; AUERBACH, Arleen D; SATAGOPAN, Jaya et al.Archives of otolaryngology, head & neck surgery. 2003, Vol 129, Num 1, pp 106-112, issn 0886-4470, 7 p.Conference Paper

FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathwayMAHMOOD ALI, Abdullah; PRADHAN, Arun; RAMSINGH SINGH, Thiyam et al.Blood. 2012, Vol 119, Num 14, pp 3285-3294, issn 0006-4971, 10 p.Article

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerREID, Sarah; SCHINDLER, Detlev; WURM, Melanie et al.Nature genetics. 2007, Vol 39, Num 2, pp 162-164, issn 1061-4036, 3 p.Article

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemiaWAGNER, John E; TOLAR, Jakub; MACMILLAN, Margaret L et al.Blood. 2004, Vol 103, Num 8, pp 3226-3229, issn 0006-4971, 4 p.Article

Stem cell transplantation for the treatment of Fanconi anaemia using a fludarabine-based cytoreductive regimen and T-cell-depleted related HLA-mismatched peripheral blood stem cell graftsBOULAD, Farid; GILLIO, Alfred; O'REILLY, Richard J et al.British journal of haematology. 2000, Vol 111, Num 4, pp 1153-1157, issn 0007-1048Article

Fludarabine-based cytoreductive regimen and T-cell-depleted grafts from alternative donors for the treatment of high-risk patients with Fanconi anaemiaCHAUDHURY, Sonali; AUERBACH, Arleen D; KERNAN, Nancy A et al.British journal of haematology. 2008, Vol 140, Num 6, pp 644-655, issn 0007-1048, 12 p.Article

The Human Variome ProjectCOTTON, Richard G. H; AUERBACH, Arleen D; FREIMER, Nelson et al.Science (Washington, D.C.). 2008, Vol 322, Num 5903, pp 861-862, issn 0036-8075, 2 p.Article