A citation-based method for searching scientific literature

Marita P McCabe, Lucy Firth, Elodie O'Connor. J Clin Psychol Med Settings 2009
Times Cited: 46







List of co-cited articles
253 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Health-related quality of life in Huntington's disease: Which factors matter most?
Aileen K Ho, Abigail S Gilbert, Sarah L Mason, Anna O Goodman, Roger A Barker. Mov Disord 2009
96
19

Quality of life in couples living with Huntington's disease: the role of patients' and partners' illness perceptions.
A A Kaptein, M Scharloo, D I Helder, L Snoei, G M J van Kempen, J Weinman, J C van Houwelingen, R A C Roos. Qual Life Res 2007
36
19

Huntington's disease from the patient, caregiver and physician's perspectives: three sides of the same coin?
Krzysztof Banaszkiewicz, Emilia J Sitek, Monika Rudzińska, Witold Sołtan, Jarosław Sławek, Andrzej Szczudlik. J Neural Transm (Vienna) 2012
42
16

The hospital anxiety and depression scale.
A S Zigmond, R P Snaith. Acta Psychiatr Scand 1983
13

Patient and caregiver quality of life in Huntington's disease.
Rebecca E Ready, Melissa Mathews, Anne Leserman, Jane S Paulsen. Mov Disord 2008
68
13

Huntington disease: clinical care and evaluation.
I Shoulson, S Fahn. Neurology 1979
571
13



Anxiety undermines quality of life in ALS patients and caregivers.
A Vignola, A Guzzo, A Calvo, C Moglia, A Pessia, E Cavallo, S Cammarosano, S Giacone, P Ghiglione, A Chiò. Eur J Neurol 2008
51
10

The emotional experiences of family carers in Huntington disease.
Janet K Williams, Heather Skirton, Jane S Paulsen, Toni Tripp-Reimer, Lori Jarmon, Meghan McGonigal Kenney, Emily Birrer, Bonnie L Hennig, Joann Honeyford. J Adv Nurs 2009
36
13

Depression and stages of Huntington's disease.
Jane S Paulsen, Carissa Nehl, Karin Ferneyhough Hoth, Jason E Kanz, Michelle Benjamin, Rachel Conybeare, Bradley McDowell, Beth Turner. J Neuropsychiatry Clin Neurosci 2005
143
10

Huntington's disease.
Marianne J U Novak, Sarah J Tabrizi. BMJ 2010
148
10


Psychopathology in verified Huntington's disease gene carriers.
E van Duijn, E M Kingma, R C van der Mast. J Neuropsychiatry Clin Neurosci 2007
188
10


Living with Huntington's disease: illness perceptions, coping mechanisms, and spouses' quality of life.
D I Helder, A A Kaptein, G M J Van Kempen, J Weinman, J C Van Houwelingen, R A C Roos. Int J Behav Med 2002
31
12


Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis.
Andrea Kübler, Susanne Winter, Albert C Ludolph, Martin Hautzinger, Niels Birbaumer. Neurorehabil Neural Repair 2005
95
8

Quality of life in ALS depends on factors other than strength and physical function.
Z Simmons, B A Bremer, R A Robbins, S M Walsh, S Fischer. Neurology 2000
177
8

Impact of Huntington's disease on quality of life.
D I Helder, A A Kaptein, G M van Kempen, J C van Houwelingen, R A Roos. Mov Disord 2001
64
8



The impact of neurological illness on marital relationships.
Elodie J O'connor, Marita P McCabe, Lucy Firth. J Sex Marital Ther 2008
28
14





"Frontal" behaviors before the diagnosis of Huntington's disease and their relationship to markers of disease progression: evidence of early lack of awareness.
Kevin Duff, Jane S Paulsen, Leigh J Beglinger, Douglas R Langbehn, Chiachi Wang, Julie C Stout, Christopher A Ross, Elizabeth Aylward, Noelle E Carlozzi, Sarah Queller. J Neuropsychiatry Clin Neurosci 2010
132
8

Well-being of family caregivers of persons with late-stage Huntington's disease: lessons in stress and coping.
Lori A Roscoe, Elizabeth Corsentino, Shirley Watkins, Marcia McCall, Juan Sanchez-Ramos. Health Commun 2009
28
14

Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis.
Francesco Pagnini, Gabriella Rossi, Christian Lunetta, Paolo Banfi, Gianluca Castelnuovo, Massimo Corbo, Enrico Molinari. Psychol Health Med 2010
77
8



Health-related quality of life in Huntington's disease: a comparison of two generic instruments, SF-36 and SIP.
Aileen K Ho, Anna O G Robbins, Stephen J Walters, Stephen Kaptoge, Barbara J Sahakian, Roger A Barker. Mov Disord 2004
43
9



'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.
Aimee Victoria Aubeeluck, Heather Buchanan, Edward J N Stupple. Qual Life Res 2012
34
11

Anxiety in Huntington's Disease.
Maria Dale, Erik van Duijn. J Neuropsychiatry Clin Neurosci 2015
38
10



Quality of life and psychosocial issues in ventilated patients with amyotrophic lateral sclerosis and their caregivers.
Dagmar Kaub-Wittemer, Nicole von Steinbüchel, Maria Wasner, Gerhard Laier-Groeneveld, Gian Domenico Borasio. J Pain Symptom Manage 2003
107
6

Major stressors facing patients with amyotrophic lateral sclerosis (ALS): a survey to identify their concerns and to compare with those of their caregivers.
Marilyn Trail, Naomi Nelson, John N Van, Stanley H Appel, Eugene C Lai. Amyotroph Lateral Scler Other Motor Neuron Disord 2004
32
9


Relatives of the impaired elderly: correlates of feelings of burden.
S H Zarit, K E Reever, J Bach-Peterson. Gerontologist 1980
6

Quality of life in ALS is maintained as physical function declines.
R A Robbins, Z Simmons, B A Bremer, S M Walsh, S Fischer. Neurology 2001
145
6

A review of psychosocial aspects of motor neurone disease.
Janet E McLeod, David M Clarke. J Neurol Sci 2007
63
6

Assessing individual quality of life in amyotrophic lateral sclerosis.
S Clarke, A Hickey, C O'Boyle, O Hardiman. Qual Life Res 2001
89
6

Caregiver quality of life in multiple sclerosis: a multicentre Italian study.
F Patti, M P Amato, M A Battaglia, M Pitaro, P Russo, C Solaro, M Trojano. Mult Scler 2007
64
6

Diagnostic criteria for multiple sclerosis: 2005 revisions to the "McDonald Criteria".
Chris H Polman, Stephen C Reingold, Gilles Edan, Massimo Filippi, Hans-Peter Hartung, Ludwig Kappos, Fred D Lublin, Luanne M Metz, Henry F McFarland, Paul W O'Connor,[...]. Ann Neurol 2005
6

Informal caregiving in multiple sclerosis patients: data from the Madrid Demyelinating Disease Group study.
Jesús Rivera-Navarro, José Manuel Morales-González, Julián Benito-León. Disabil Rehabil 2003
50
6

Work and recreational changes among people with neurological illness and their caregivers.
Marita P McCabe, Candice Roberts, Lucy Firth. Disabil Rehabil 2008
26
11


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.