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Increased risk of lymphoid neoplasm in patients with myeloproliferative neoplasm: a study of 1,915 patientsRUMI, Elisa; PASSAMONTI, Francesco; ELENA, Chiara et al.Haematologica (Roma). 2011, Vol 96, Num 3, pp 454-458, issn 0390-6078, 5 p.Article

The Impact of Substance Use on Brain Structure in People at High Risk of Developing SchizophreniaWELCH, Killian A; MCINTOSH, Andrew M; JOB, Dominic E et al.Schizophrenia bulletin. 2011, Vol 37, Num 5, pp 1066-1076, issn 0586-7614, 11 p.Article

The Relationship Between Smoking and Replicated Sequence Variants on Chromosomes 8 and 9 With Familial Intracranial AneurysmDEKA, Ranjan; KOLLER, Daniel L; ANDERSON, Craig et al.Stroke (1970). 2010, Vol 41, Num 6, pp 1132-1137, issn 0039-2499, 6 p.Article

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosisHOI SOO YOON; KIM, Hee-Jin; BAE, Keun-Wook et al.Haematologica (Roma). 2010, Vol 95, Num 4, pp 622-626, issn 0390-6078, 5 p.Article

Genome-Wide Linkage Scan for Prostate Cancer Susceptibility From the University of Michigan Prostate Cancer Genetics Project : Suggestive Evidence for Linkage at 16q23LANGE, Ethan M; BEEBE-DIMMER, Jennifer L; RAY, Anna M et al.The Prostate. 2009, Vol 69, Num 4, pp 385-391, issn 0270-4137, 7 p.Article

Nonagenarian Siblings and Their Offspring Display Lower Risk of Mortality and Morbidity than Sporadic Nonagenarians: The Leiden Longevity StudyWESTENDORP, Rudi G. J; VAN HEEMST, Diana; ROZING, Maarten P et al.Journal of the American Geriatrics Society. 2009, Vol 57, Num 9, pp 1634-1637, issn 0002-8614, 4 p.Article

A review of mathematical models used to determine sperm donor limits for infertility treatmentSAWYER, Neroli; MCDONALD, John.Fertility and sterility. 2008, Vol 90, Num 2, pp 265-271, issn 0015-0282, 7 p.Article

Exclusion of Linkage to Chromosome 14q in a Large South Tyrolean Family With Idiopathic Basal Ganglia Calcification (IBGC)BEU VOLPATO, Claudia; DE GRANDI, Alessandro; BUFFONE, Ebba et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1319-1322, issn 1552-4841, 4 p.Article

Rectal gastrointestinal stromal tumors associated with a novel germline KIT mutationWOZNIAK, Agnieszka; RUTKOWSKI, Piotr; SCIOT, Raf et al.International journal of cancer. 2008, Vol 122, Num 9, pp 2160-2164, issn 0020-7136, 5 p.Article

Centenarian Offspring : Start Healthier and Stay HealthierADAMS, Emily R; NOLAN, Vikki G; ANDERSEN, Stacy L et al.Journal of the American Geriatrics Society. 2008, Vol 56, Num 11, pp 2089-2092, issn 0002-8614, 4 p.Article

BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarraysBANE, Anita L; BECK, Jeanne C; JOHN, Esther M et al.The American journal of surgical pathology. 2007, Vol 31, Num 1, pp 121-128, issn 0147-5185, 8 p.Article

Acute aortic dissection in children and adolescents : Diagnostic and after-event follow-up obligation to the patient and familyFIKAR, Charles R.Clinical cardiology (Mahwah, NJ). 2006, Vol 29, Num 9, pp 383-386, issn 0160-9289, 4 p.Article

Evidence for increased clinical severity of familial and sporadic Paget's disease of bone in Campania, southern ItalyRENDINA, Domenico; GENNARI, Luigi; DE FILIPPO, Gianpaolo et al.Journal of bone and mineral research (Print). 2006, Vol 21, Num 12, pp 1828-1835, issn 0884-0431, 8 p.Article

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma casesPAL, Tuya; PERMUTH-WEY, Jenny; WILBANKS, George et al.Cancer. 2005, Vol 104, Num 12, pp 2807-2816, issn 0008-543X, 10 p.Article

Low-density lipoprotein receptor genotype and response to pravastatin in children with familial hypercholesterolemia : Substudy of an intima-media thickness trialKOEIJVOETS, Kristel C. M. C; RODENBURG, Jessica; HUTTEN, Barbara A et al.Circulation (New York, N.Y.). 2005, Vol 112, Num 20, pp 3168-3173, issn 0009-7322, 6 p.Article

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Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancerNAN HU; CHAOYU WANG; HAN, Xiao-You et al.Oncogene (Basingstoke). 2004, Vol 23, Num 3, pp 852-858, issn 0950-9232, 7 p.Article

A novel mutation in the SDHD gene in a family with inherited paragangliomas-implications of genetic diagnosis for follow up and treatmentRENARD, Laurette; GODFRAIND, Catherine; BOON, Laurence M et al.Head & neck. 2003, Vol 25, Num 2, pp 146-151, issn 1043-3074, 6 p.Article

Familial early-onset progressive vestibulopathy without hearing impairmentBRANTBERG, Krister.Acta oto-laryngologica. 2003, Vol 123, Num 6, pp 713-717, issn 0001-6489, 5 p.Article

Familial predisposition to tufted angioma: identification of blood and lymphatic vascular componentsTILLE, J.-C; MORRIS, M. A; BRÜNDLER, M.-A et al.Clinical genetics. 2003, Vol 63, Num 5, pp 393-399, issn 0009-9163, 7 p.Article

Familial Intracranial Aneurysms: Is Anatomic Vulnerability Heritable?MACKEY, Jason; BROWN, Robert D; MEISSNER, Irene et al.Stroke (1970). 2013, Vol 44, Num 1, pp 38-42, issn 0039-2499, 5 p.Article

Depressive symptoms are associated with (sub)clinical psychotic symptoms in patients with non-affective psychotic disorder, siblings and healthy controlsKLAASSEN, R. M. C; HEINS, M; LUTEIJN, L. B et al.Psychological medicine (Print). 2013, Vol 43, Num 4, pp 747-756, issn 0033-2917, 10 p.Article

Inherited Mosaicism for the Supernumerary Marker Chromosome in Cat Eye Syndrome: Inter- and Intra-Individual Variation and Correlation to the PhenotypeKVARNUNG, Malin; LINDSTRAND, Anna; MALMGREN, Helena et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 5, pp 1111-1117, issn 1552-4825, 7 p.Article

Leucémies lymphoïdes chroniques (LLC) familiales: état des lieux = Familial Chronic lymphoid leukemia (CLL): state of the artCHOQUET, Sylvain.Hématologie (Montrouge). 2012, Vol 18, Num 3, pp 182-188, issn 1264-7527, 7 p.Article